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cuboid. The joints are approximately on an imaginary line traced from muscles that produce this motion are tibialis anterior and fibularis
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AnklE And fooT 1438 9 noITCES longus. Flexion and extension are brought about by the long and short ments of adjoining metatarsophalangeal joints. The interossei are flexors and extensors of the toes. Movement between the medial cunei­ dorsal to, and the lumbricals, digital vessels and nerves are plantar to, form and first metatarsal, and between the fourth and fifth metatarsal these ligaments. They resemble the deep transverse metacarpal liga­ bases and the cuboid, is moderate and allows the foot to adapt to ments except that, in the foot, there is a deep transverse metatarsal liga­ uneven surfaces, whereas movement between the second and third ment between the plantar ligament of the second metatarsophalangeal metatarsal bases and their corresponding cuneiforms is very limited. joint and that of the first metatarsophalangeal joint (see Fig. 84.17). Collateral ligaments The collateral ligaments are strong cords flanking INTERMETATARSAL JOINTS each joint. They are attached to the dorsal tubercles on the metatarsal heads and the corresponding side of the phalangeal bases, and they The intermetatarsal ligaments are very strong and are present between slope inferodistally. The first metatarsophalangeal joint also contains all the lateral four metatarsals; they are absent between the first and metatarsosesamoid ligaments. On either side, the ligaments arise from second metatarsals. The base of the second metatarsal is joined to the metatarsal head with a narrow origin and then fan out to insert on the first tarsometatarsal joint by the cuneometatarsal interosseous the border of the proximal phalanx and the plantar plate. Each collat­ ligament. eral ligament consists of the phalangeal collateral ligament, which inserts into the base of the proximal phalanx, and the accessory col­ Ligaments The ligaments of the intermetatarsal joints include the lateral ligament, which inserts into the plantar plate. dorsal and plantar intermetatarsal ligaments. Synovial membrane Each metatarsophalangeal joint is a separate
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Dorsal and plantar intermetatarsal ligaments As with their dorsal synovial joint. counterparts, the plantar intermetatarsal ligaments are longitudinal, oblique or transverse and they vary considerably in both number and Innervation The main nerve supply of the metatarsophalangeal joints organization. The plantar ligaments are significantly stronger than the is from the plantar digital nerves, which supply the first, second, third corresponding dorsal ligaments. The strongest is the second oblique and medial half of the fourth metatarsophalangeal joint on their plantar plantar ligament, which connects the medial cuneiform to the bases of aspects. Digital branches of the lateral plantar nerve supply the lateral the second and third metatarsals. half of the fourth joint, and both medial and lateral aspects of the fifth joint, on their plantar sides. The medial dorsal cutaneous branch of the Other ligaments All the metatarsal heads are connected indirectly by superficial fibular nerve supplies the dorsomedial side of the hallucal deep transverse metatarsal ligaments. Dorsal and plantar ligaments pass metatarsophalangeal joint. The deep fibular nerve supplies the dorso­ transversely between adjacent bases; interosseous ligaments are strong lateral side of the hallucal metatarsophalangeal joint and the medial transverse bands that connect non­articular parts of the adjacent sur­ side of the metatarsophalangeal joint of the second toe. faces (see Fig. 84.17). Relations Dorsally, the tendon of extensor hallucis longus lies medial to the tendon of extensor hallucis brevis. The same arrangement occurs METATARSOPHALANGEAL JOINTS in the lateral four toes with the tendons of extensor digitorum longus and brevis. The interossei are plantarmedial and plantarlateral, dorsal Metatarsophalangeal articulations are ovoid or ellipsoid joints between to the transverse intermetatarsal ligament, whereas the lumbrical ten­ the rounded metatarsal heads and shallow cavities on the proximal dons and the digital artery and nerve are plantar to the transverse phalangeal bases. They are usually 2.5 cm proximal to the web spaces intermetatarsal ligament. The extrinsic and intrinsic flexors lie on the
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of the toes. plantar aspect of the joint in the midline. If approaching the metatar­ sophalangeal joint surgically from the plantar surface, it is important Articulating surfaces Articular surfaces cover the distal and plantar, not to stray from the midline. but not the dorsal, aspects of the metatarsal heads. The plantar aspect of the first metatarsal head has two longitudinal grooves separated by Factors maintaining stability The first metatarsophalangeal joint a ridge (the crista). Each articulates with a sesamoid bone embedded owes its stability to its capsuloligamentous structures, and to flexor and in the capsule of the joint, formed here by the two tendons of flexor extensor hallucis brevis, with a small contribution from flexor and hallucis brevis. The sesamoid bones are connected to each other by the extensor hallucis longus or the bony contours. The collateral ligaments intersesamoid ligament, which forms the floor of the tendinous canal and plantar plates stabilize the metatarsophalangeal joints of the lateral for the tendon of flexor hallucis longus. The medial sesamoid bone four toes. Rupture of the plantar plate can lead to dislocation of the receives an attachment from abductor hallucis and the lateral sesamoid metatarsophalangeal joint and, possibly, hammer toe deformity. bone receives an attachment from adductor hallucis, forming the con­ joint tendon. Muscles producing movement The types of movements that Articular areas on the proximal phalangeal bases are concave. occur at these joints are like those that occur at the corresponding joints The ligaments are capsular, plantar, deep transverse metatarsal and in the hand, but the range of movement is quite different. In contrast collateral. to the metacarpophalangeal joints, the range of active extension that can occur at the metatarsophalangeal joints (50–60°) is greater than Fibrous capsules Fibrous capsules are attached to their articular that of flexion (30–40°); this is an adaptation to the needs of walking, margins. They are thin dorsally, and may be separated from the extrinsic and is most marked in the joint of the great toe, where flexion is a few
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extensor tendons by small bursae, or they may be replaced by the degrees while extension may reach 90°. When the foot is on the ground, tendons, but they are inseparable from the plantar and collateral liga­ metatarsophalangeal joints are already extended to at least 25° because ments. The plantar aponeurosis blends with the plantar capsule to form the metatarsals incline proximally in the longitudinal arches of the foot the so­called ‘plantar plate’, which inserts distally into the base of the (see Fig. 84.8A). The range of passive movements in these joints is 90° proximal phalanx via medial and lateral bundles. Proximally, the plate (extension) and 45° (flexion), according to Kapandji (2011). The fol­ is attached to the metatarsal head via a thin synovial fold. It also receives lowing muscles produce movements at the metatarsophalangeal joints: an attachment from the accessory collateral ligament. Flexion Flexor digitorum brevis, lumbricals and interossei, assisted by Ligaments The ligaments of the metatarsophalangeal joints are the flexor digitorum longus and flexor accessorius. In the fifth toe, flexor plantar, deep transverse metatarsal and collateral ligaments. digiti minimi brevis assists. For the great toe, flexors hallucis longus and brevis and the oblique head of the adductor hallucis are the only flexors. Plantar ligaments The plantar ligaments are thick and dense. They lie between and blend with the collateral ligaments, being loosely attached Extension Extensors digitorum longus and extensor digitorum brevis, to the metatarsals and firmly attached to the phalangeal bases. Their extensor hallucis longus. margins blend with the deep transverse metatarsal ligaments. Their plantar surfaces are grooved for the flexor tendons, the fibrous sheaths Adduction Adductor hallucis; in the third to fifth toes, the first, second of which connect with the edges of the grooves, and their deep surfaces and third plantar interossei, respectively. extend the articular areas for metatarsal heads. Abduction Abductor hallucis; in the second toe, the first and second
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Deep transverse metatarsal ligaments The deep transverse metatarsal dorsal interossei; in the third and fourth toes, the corresponding dorsal ligaments are four short, wide, flat bands that unite the plantar liga­ interossei; in the fifth toe, abductor digiti minimi.
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Arches of the foot 1439 48 RETPAHC Note that the line of reference for adduction and abduction is along (Hicks 1954). Dorsiflexion, especially of the great toe, draws the two the second digit, which has the least mobile metatarsal. The second toe pillars together, thus heightening the arch: the so­called ‘windlass’ may therefore be ‘abducted’ medially and laterally by the first and mechanism. Next in importance is the spring ligament, which supports second dorsal interossei, respectively. the head of the talus. If this ligament fails, the navicular and calcaneus separate, allowing the talar head, which is the highest point of the arch, Hallux valgus Hallux valgus is a common condition, occurring to descend, leading to a flat­foot deformity. The talocalcaneal ligaments mainly in individuals who have a genetic predisposition. Footwear is and the anterior fibres of the deltoid ligament, from the tibia to the implicated in the condition, which presumably accounts for the greater navicular, also contribute to the stability of the arch. incidence in females. Metatarsus primus varus, an adduction deformity Muscles play a role in the maintenance of the medial longitudinal of the first metatarsal, is commonly associated with hallux valgus. arch. Flexor hallucis longus acts as a bowstring. Flexor digitorum longus, The more spheroidal the shape of the first metatarsal head, the more abductor hallucis and the medial half of flexor digitorum brevis also likely it is to be unstable. Conversely, a flat metatarsal head is less likely contribute but to a lesser extent. Tibialis posterior and anterior invert to be associated with hallux valgus. No muscle inserts into the first and adduct the foot, and so help to raise its medial border. The impor­ metatarsal head, and therefore its position is determined by the posi­ tance of tibialis posterior is manifest by the collapse of the medial tion of the proximal phalanx. As the proximal phalanx moves laterally longitudinal arch that accompanies failure of its tendon (see below). on the metatarsal head, it pushes the head medially. This leads to
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attenuation of the medial soft tissue structures and contracture of the Lateral longitudinal arch lateral ones. The sesamoid sling (i.e. plantar plate and flexor hallucis brevis), which is anchored laterally by adductor hallucis, remains in The lateral longitudinal arch is a much less pronounced arch than the place as the head moves medially, displacing the sesamoid bones from medial one. The bones making up the lateral longitudinal arch are the beneath the metatarsal head. As this happens, the weakest point of the calcaneus, the cuboid and the fourth and fifth metatarsals; they con­ medial capsule fails, so that abductor hallucis slips under the metatarsal tribute little to the arch in terms of stability (see Fig. 84.8A). The pillars head. This leads to failure of the intrinsic muscles to stabilize the joint, are the calcaneus posteriorly and the lateral two metatarsal heads ant­ and the pull of abductor hallucis leads to spinning of the proximal eriorly. Ligaments play a more important role in stabilizing the arch, phalanx, which results in a varus deformity. Failure to intervene surgi­ especially the lateral part of the plantar aponeurosis and the long and cally inevitably results in a progressive deformity. short plantar ligaments. However, the tendon of fibularis longus makes the most important contribution to the maintenance of the lateral arch. INTERPHALANGEAL JOINTS The lateral two tendons of flexor digitorum longus (and flexor acces­ sorius), the muscles of the first layer (lateral half of flexor digitorum brevis and abductor digiti minimi), and fibularis brevis and tertius also Interphalangeal articulations are almost pure hinge joints, in which the contribute to the maintenance of the lateral longitudinal arch. trochlear surfaces on the phalangeal heads articulate with reciprocally curved surfaces on adjacent phalangeal bases. Each has an articular Transverse arch capsule and two collateral ligaments, as occurs in the metatarsophalan­ geal joints. The plantar surface of the capsule is a thickened fibrous
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plate, like the plantar metatarsophalangeal ligaments, and is often The bones involved in the transverse arch are the bases of the five meta­ termed the plantar ligament. tarsals, the cuboid and the cuneiforms (see Fig. 84.8A). The intermedi­ ate and lateral cuneiforms are wedge­shaped and thus adapted to Innervation The interphalangeal articulations are innervated by maintenance of the transverse arch. The ligaments, which bind the branches from the plantar digital nerves. The medial dorsal cutaneous cuneiforms and the metatarsal bases, mainly provide the stability of the branch of the superficial fibular nerve also supplies the interphalangeal arch, as does the tendon of fibularis longus, which tends to approximate joint of the great toe. Branches of the deep fibular, intermediate dorsal the medial and lateral borders of the foot. A shallow arch is maintained cutaneous and sural nerves sometimes supply the joints of the lateral at the metatarsal heads by the deep transverse ligaments, transverse four toes. fibres that tie together the digital slips of the plantar aponeurosis, and, to a lesser extent, by the transverse head of adductor hallucis. Muscles producing movement Movements are flexion and exten­ sion, which are greater in amplitude between the proximal and middle Pes planus and pes cavus phalanges than between the middle and distal. Flexion is marked, but extension is limited by tension of the flexor muscles and plantar liga­ The term pes planus denotes an excessively flat foot. There is no precise ments. Abduction, adduction and rotation occur to a minor extent. The degree of flatness that defines pes planus but it may be either physiologi­ following muscles produce movements at the interphalangeal joints: cal or pathological. In physiological pes planus, the feet are flexible and rarely problematic. There is a high prevalence in children of preschool Flexion Flexor digitorum longus, flexor digitorum brevis, and flexor age. In the age group 2–6 years, normal arch volumes in the sitting and hallucis longus. Flexor accessorius assists flexor digitorum longus to standing positions correlate with the height of the navicular (lowest
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maintain an extended toe and neutralize the medial pull of flexor digi­ palpable medial projection of the navicular to the floor (Chang et al torum longus. 2012)). In marked contrast, pathological pes planus is often associated with stiffness and pain. The windlass (or ‘Jack’s great toe’) test involves Extension Extensor digitorum longus, extensor digitorum brevis, exten­ passively dorsiflexing the great toe at the metatarsophalangeal joint. sor hallucis longus and extensor hallucis brevis. This tightens the plantar aponeurosis and, in flexible pes planus, results in accentuation of the medial longitudinal arch. In pathological pes ARCHES OF THE FOOT planus, no accentuation of the arch is seen. This test can also be carried out by asking the individual to stand with both feet plantar flexed while viewing the hindfoot from behind. In flexible flat feet, the calcaneus Three main arches are recognized in the foot. They are the medial lon­ swings into a varus position; in pathological pes planus it does not. gitudinal, the lateral longitudinal and the transverse arches. The roles Causes of pathological pes planus include tarsal coalition, disruption of the arches of the foot in standing, walking and running are discussed of the tendon of tibialis posterior, rupture of the spring ligament, tar­ later in this chapter. sometatarsal arthritis (and subsequent collapse), and hindfoot (talocal­ caneal or subtalar joint) degenerative or inflammatory arthritis. Medial longitudinal arch Pes cavus denotes an excessively high­arched foot. The majority of cases arise as a result of a neurological disorder (e.g. Charcot–Marie– The medial margin of the foot arches up between the heel proximally Tooth disease, tethered spinal cord, poliomyelitis). According to the and the medial three metatarsophalangeal joints to form a visible arch anatomical location of the deformity, pes cavus may be classified into (see Fig. 84.8A). It is made up of the calcaneus, talar head, navicular, hindfoot, midfoot or forefoot cavus. When pes cavus involves all three
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the three cuneiforms and the medial three metatarsals. The posterior parts of the foot, it is called ‘global’ cavus. and anterior pillars are the posterior part of the inferior calcaneal surface In Charcot–Marie–Tooth disease, an overactive fibularis longus leads and the three metatarsal heads, respectively. The bones themselves con­ to plantar hyperflexion of the first metatarsal. To keep the forefoot in tribute little to the stability of the arch, whereas the ligaments contribute contact with the ground, the patient develops a progressive compens­ significantly. The most important ligamentous structure is the plantar atory hindfoot varus. If ignored, the hindfoot varus, which is initially aponeurosis, which acts as a tie beam between the supporting pillars flexible, becomes fixed.
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AnklE And fooT 1440 9 noITCES section (Ahmed et al 1998, Zantop et al 2003, Chen et al 2009). The MUSCLES posterior tibial artery primarily supplies the proximal and distal sec­ tions, and the midsection receives a relatively poor blood supply from The muscles acting on the foot may be divided into extrinsic and intrin­ the fibular artery (Chen et al 2009). These findings support previous sic groups. work showing that the hypovascular midsection of the calcaneal tendon is the area most prone to rupture and also underscore the importance of avoiding disruption of the vascular supply to the tendon EXTRINSIC MUSCLES during percutaneous surgery. The vascularity of the skin overlying the calcaneal tendon varies according to location: the skin on the medial The extrinsic muscles are described in Chapter 83. Their tendons cross side of the tendon is supplied by the posterior tibial artery and on the the ankle, and move and stabilize this joint. Distally, the tendons also lateral side by the fibular artery (Yepes et al 2010). The skin covering act on the joints of the foot and help to stabilize them. The muscles the posterior aspect of the tendon is the most poorly vascularized; can be grouped according to their arrangement in the leg. The extensors medial or lateral incisions of the skin surrounding the tendon should arise in the anterior compartment of the leg and their tendons pass reduce post­surgical healing complications relative to a direct posterior anterior to the ankle, where they are bound down by the extensor reti­ approach. nacula. The lateral group arises in the relatively narrow lateral compart­ The calcaneal tendon is not the only plantar flexor of the ankle, ment of the leg and their tendons pass posterior to the lateral malleolus, which is one of the reasons that ruptures of the calcaneal tendon may bound down by the fibular retinacula. The flexors arise in the posterior not always be clinically apparent. However, it is a frequent site of compartment of the leg and their tendons pass posterior to the ankle, pathology because of its susceptibility to rupture, degenerative change
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where the tendons of the superficial group of flexors are inserted into (tendinosis) and inflammation (paratendinitis); the area of relative the calcaneus (see below), and the tendons of the deep group of flexors avascularity in the mid­substance of the tendon is where the majority are bound down by the flexor retinaculum. of problems occur. Anterior group Relations The calcaneal tendon is subcutaneous. The sural nerve crosses its lateral border about 10 cm above its insertion; the nerve is Tibialis anterior, extensor hallucis longus, extensor digitorum longus especially vulnerable here to iatrogenic injury during surgery. Distally, and fibularis tertius are described on pages 1406–1408. there are bursae superficial and deep to the tendon. The muscle belly of flexor hallucis longus lies deep to the deep fascia on the anterior Lateral group surface of the tendon. Actions The calcaneal tendon produces plantar flexion of the ankle Fibularis longus and fibularis brevis are described on page 1408. joint. The tendon fibres spiral laterally through 90° as they descend, so that the fibres associated with gastrocnemius come to insert on the bone Posterior group more laterally, and those associated with soleus more medially. Superficial group Heel bursae There are three locations about the heel where bursae Gastrocnemius, soleus and plantaris are described on pages 1409–1410; occur. The most common is the retrocalcaneal bursa, which lies between the calcaneal tendon is described below. the calcaneal tendon and the posterior surface of the calcaneus. An almost constant finding, it has an anterior bursal wall composed of Calcaneal (Achilles) tendon fibrocartilage and a thin posterior wall, which blends with the thin The calcaneal tendon is the common tendon of gastrocnemius and epitenon (epitendineum) of the calcaneal tendon. Dorsiflexion of the soleus. It is the thickest and strongest tendon in the human body (see ankle results in compression of the bursa. Less common are an adventi­
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Fig. 82.3). Approximately 15 cm long, it begins near the middle of the tious bursa superficial to the calcaneal tendon, and a subcalcaneal bursa calf; its anterior surface receives muscle fibres from soleus almost to its between the inferior surface of the calcaneus and the origin of the inferior end. It gradually becomes more rounded until approximately plantar aponeurosis. A prominent superolateral calcaneal tuberosity 4 cm above the calcaneus; below this level, it expands and becomes may impinge on the deep aspect of the calcaneal tendon where it inserts attached to the midpoint of the posterior surface of the calcaneus. Age­ on to the calcaneus (Haglund’s disease). It is often associated with a dependent variability in the terminal insertion site of the calcaneal retrocalcaneal bursa, and symptoms are exacerbated by dorsiflexion of tendon (Snow et al 1995, Kim et al 2010, Kim et al 2011) may explain the ankle because this movement increases the pressure within the why calcaneal tendinopathy is infrequently found in children and adol­ bursa and causes impingement of calcaneus against the tendon escents. It also has implications for the appropriate siting of surgical insertion. entry portals about the calcaneal tendon insertion in order to reduce the risk of iatrogenic injury to the tendon (Lohrer et al 2008). The fibres Plantaris of the calcaneal tendon are not aligned strictly vertically and they Plantaris is described on page 1410. display a variable degree of spiralization (Cummins and Anson 1946). Deep group The tendon fibres spiral laterally through 90° as they descend, so that the fibres associated with gastrocnemius come to insert on the The deep muscles of the calf include popliteus, which acts on the knee calcaneus more laterally, and those associated with soleus more medi­ joint, and flexor hallucis longus, flexor digitorum longus and tibialis ally. The fibres in the tendon of plantaris (described in Ch. 83) exhibit posterior, which all act on the ankle joint and joints of the foot. varying degrees of blending with the fibres of the calcaneal tendon,
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sometimes blending entirely at its insertion or inserting into the plantar flexor hallucis longus aponeurosis. Flexor hallucis longus is described on page 1411. The tendon of flexor hallucis longus is described below. Tensile properties The estimated tensile breaking load of a fetal calcaneal tendon increases from 2 kg at 6 months post fertilization to flexor digitorum longus 18 kg at full term (Yamada 1970). In adults, the average estimated Flexor digitorum longus is described on page 1410. tensile breaking load of the calcaneal tendon is 192 kg, decreasing to 160 kg in the eighth decade (Takigawa 1953), which may explain why Tibialis posterior calcaneal tendon ruptures are infrequently encountered in youth Tibialis posterior is described on page 1412. (Yamada 1970). Vascular supply The blood supply to the calcaneal tendon is poor; INTRINSIC MUSCLES the predominant artery is a recurrent branch of the posterior tibial artery, which mainly supplies peritendinous tissues (Salmon et al The intrinsic muscles, i.e. those contained entirely within the foot, 1994). There is an additional supply from the paratenon (Carr and follow the primitive limb pattern of plantar flexors and dorsal Norris 1989, Chen et al 2009), as well as a supply proximally from extensors. intramuscular arterial branches and distally from the calcaneus. Micro­ The plantar muscles may be divided into medial, lateral and inter­ dissection and angiographic studies have identified three main vascular mediate groups. The medial and lateral groups consist of the intrinsic territories: a proximal section, a hypovascular midsection and a distal muscles of the great and fifth toes, respectively, and the central or
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48 RETPAHC Ankle and foot 1 17 14 2 16 1 3 15 4 13 5 12 2 11 6 14 3 A 4 13 7 8 9 10 5 12 6 1 11 16 15 7 10 2 14 9 13 8 12 B 3 11 10 4 9 5 8 C 6 7 Fig. 84.19 Turbo spin-echo, T1-weighted magnetic resonance (MR) images of the left ankle of a woman aged 26. A, A coronal turbo spin-echo, T1-weighted MR image of the forefoot through a metatarsal. Key: 1, extensor hallucis longus tendon; 2, first metatarsal; 3, adductor hallucis, oblique head; 4, flexor hallucis (medial head); 5, flexor hallucis (lateral head); 6, flexor hallucis longus tendon; 7, flexor digitorum longus tendons; 8, third metatarsal; 9, fourth metatarsal; 10, flexor digiti minimi brevis; 11, abductor digiti minimi; 12, fifth metatarsal; 13, dorsal interossei; 14, second metatarsal. B, An axial turbo spin-echo, T1-weighted MR image of the ankle. Key: 1, deep fibular nerve; 2, tibia; 3, tendon of tibialis posterior; 4, tendon of flexor digitorum longus; 5, posterior tibial artery; 6, tibial nerve (early medial and lateral plantar branching); 7, tendon of flexor hallucis longus; 8, calcaneal tendon; 9, soleus; 10, sural nerve; 11, flexor hallucis longus; 12, fibularis brevis; 13, tendon of fibularis longus; 14, fibula; 15, extensor digitorum longus;
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16, extensor hallucis longus; 17, tendon of anterior tibialis. C, A sagittal turbo spin-echo, T1-weighted MR image of the ankle and hindfoot. Key: 1, flexor digitorum longus; 2, soleus; 3, talocalcaneal (subtalar) joint; 4, calcaneal tendon; 5, calcaneus; 6, flexor digitorum brevis; 7, flexor accessorius; 8, cuboid; 9, lateral cuneiform; 10, intermediate cuneiform; 11, navicular; 12, talocalcaneal interosseous ligament; 13, talus; 14, talocrural joint; 15, tibia; 16, tibialis anterior. (Courtesy of Robert J. Ward, MD, Tufts University School of Medicine, Boston, MA.) 1440.e1
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Muscles 1441 48 RETPAHC A B Tendon of flexor hallucis longus Tendinous Cruciform Tendinous sheath of sheath of part toes Anular great toe part Tendinous sheath of toes Tendon of flexor Tendons of flexor hallucis longus digitorum longus Tendons of First to fourth Flexor hallucis Adductor hallucis, flexor digitorum lumbricals brevis transverse head brevis Adductor hallucis, transverse head First to fourth Flexor hallucis brevis lumbricals Third plantar Flexor digiti interosseus Tendon of minimi brevis flexor digitorum longus Abductor digiti Abductor digiti minimi minimi Plantar tendinous sheath of Abductor hallucis Flexor digiti minimi brevis fibularis longus Fourth dorsal interosseus Tendon of Flexor digitorum brevis flexor hallucis longus Tendon of fibularis longus Plantar aponeurosis Abductor hallucis Flexor accessorius Abductor digiti minimi Flexor digitorum brevis Calcaneal tuberosity Calcaneal tuberosity Fig. 84.20 Muscles of the sole of the foot. A, First layer. B, Second layer. (With permission from Waschke J, Paulsen F (eds), Sobotta Atlas of Human Anatomy, 15th ed, Elsevier, Urban & Fischer. Copyright 2013.) intermediate group includes the lumbricals, interossei and intrinsic Clinical anatomy Abductor hallucis fascia is strong and can be used digital flexors. It is customary to group the muscles in four layers in soft tissue augmentation following correction of hallux valgus because this is the order in which they are encountered during dissec­ deformity. Rarely, persistent, exaggerated tonus in the muscle may be a tion. In clinical practice and in terms of function, however, the former cause of varus deformity of the foot, necessitating surgical intervention. grouping is often more useful. The vascular supply and innervation of An abductor hallucis flap is sometimes used for provision of soft tissue
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the intrinsic muscles of the foot are given at the end of this section. coverage. Plantar muscles of the foot: first layer Flexor digitorum brevis Attachments Flexor digitorum brevis arises by a narrow tendon from This superficial layer includes abductor hallucis, abductor digiti minimi the medial process of the calcaneal tuberosity, from the central part of and flexor digitorum brevis (Fig. 84.20). All three extend from the the plantar aponeurosis, and from the intermuscular septa between it calcaneal tuberosity to the toes, and all assist in maintaining the concav­ and adjacent muscles (see Fig. 84.20A). It divides into four tendons, ity of the foot. which pass to the lateral four toes; the tendons enter digital tendinous sheaths accompanied by the tendons of flexor digitorum longus, which Abductor hallucis lie deep to them. At the bases of the proximal phalanges, each tendon Attachments Abductor hallucis arises principally from the flexor divides around the corresponding tendon of flexor digitorum longus; retinaculum, but also from the medial process of the calcaneal tuberos­ the two slips then reunite and partially decussate, forming a tunnel ity, the plantar aponeurosis, and the intermuscular septum between this through which the tendon of flexor digitorum longus passes to the muscle and flexor digitorum brevis. The muscle fibres end in a tendon distal phalanx. The tendon of flexor digitorum brevis divides again and that is attached, together with the medial tendon of flexor hallucis attaches to both sides of the shaft of the middle phalanx. The way in brevis, to the medial side of the base of the proximal phalanx of the which the tendon of flexor digitorum brevis divides and attaches to the great toe. Frequently, some fibres are attached more proximally to the phalanges is identical to that of the tendons of flexor digitorum super­ medial sesamoid bone of this toe. The muscle may also send some ficialis in the hand. The slip to a given toe may be absent, or it may be
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fibres to the dermis along the medial border of the foot. replaced by a small muscular slip from the extrinsic flexor tendons or from flexor accessorius. Conversely, the slip may be joined by a second, Relations Abductor hallucis lies along the medial border of the foot supernumerary slip. and covers the origins of the plantar vessels and nerves (Fig. 84.21). The space created for the plantar nerves and vessels by abductor hallucis Relations Flexor digitorum brevis lies immediately deep to the central and its relationship to the calcaneus is called the porta pedis. part of the plantar aponeurosis (see Fig. 84.20A). Its deep surface is separated from the lateral plantar vessels and nerves by a thin layer of Actions Abductor hallucis produces abduction of the great toe relative fascia. to the longitudinal axis of the foot at the shaft of the second metatarsal. Actions Flexor digitorum brevis flexes the lateral four toes at the Testing Abductor hallucis is tested clinically by instructing the subject proximal interphalangeal joint, with equal effect in any position of the to resist a forcibly applied lateral deviation of the proximal phalanx. ankle joint.
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AnklE And fooT 1442 9 noITCES Flexor tendinous sheaths The terminations of the tendons of the extrinsic and intrinsic flexor muscles are contained in osseo­aponeurotic canals similar to those that occur in the fingers. These canals are bounded above by the phalanges Tendons of and below by fibrous bands, the digital fibrous sheaths, which arch Proper plantar digital flexor digitorum brevis across the tendons and attach on either side to the margins of the arteries phalanges (see Fig. 84.20A). Along the proximal and middle phalanges, the fibrous bands are strong and the fibres are transverse (anular part); Common plantar digital arteries opposite the joints they are much thinner and the fibres decussate Tendon of flexor (cruciform part). Each osseo­aponeurotic canal has a synovial lining, hallucis longus which is reflected around its tendon; within this sheath, vincula tendi­ Flexor hallucis Common plantar num are arranged as they are in the fingers. brevis digital nerves Flexor accessorius (quadratus plantae) Tendons of flexor Attachments Flexor accessorius (quadratus plantae) arises by two digitorum longus heads, with the long plantar ligament situated deeply in the interval between the two heads (see Figs 84.20B, 84.19C). The medial head is Superficial Lateral larger and is attached to the medial concave surface of the calcaneus, branch plantar below the groove for the tendon of flexor hallucis longus. The lateral nerve Deep branch head is flat and tendinous, and is attached to the calcaneus distal to the Abductor hallucis lateral process of the tuberosity, and to the long plantar ligament. The muscle belly inserts into the tendon of flexor digitorum longus at the Flexor accessorius point where it is bound by a fibrous slip to the tendon of flexor hallucis longus and where it divides into its four tendons. Cutaneous branch Lateral plantar artery The muscle is sometimes absent altogether. Its distal attachment to the tendons of flexor digitorum longus may vary, which means that the Medial plantar nerve
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Abductor digiti minimi fourth and fifth long flexor tendons may, at times, fail to receive slips Flexor retinaculum from the flexor accessorius. Plantar aponeurosis Muscular branch Flexor digitorum brevis Relations The medial plantar nerve passes medial to and the lateral Posterior tibial artery plantar nerve passes superficial to flexor accessorius. Lateral plantar nerve Actions By pulling on the tendons of flexor digitorum longus, flexor accessorius provides a means of flexing the lateral four toes in any posi­ tion of the ankle joint. Abductor hallucis Calcaneal anastomosis Lumbrical muscles Attachments The lumbrical muscles are four small muscles (num­ Fig. 84.21 Plantar nerves and vessels in relation to muscle layers. (With bered from the medial side of the foot) that are accessory to the tendons permission from Waschke J, Paulsen F (eds), Sobotta Atlas of Human of flexor digitorum longus (see Fig. 84.20). They arise from these Anatomy, 15th ed, Elsevier, Urban & Fischer. Copyright 2013.) tendons as far back as their angles of separation, each springing from the sides of two adjacent tendons, except for the first lumbrical, which arises only from the medial border of the first tendon. The muscles end in tendons that pass distally on the medial sides of the four lateral toes Testing To test the action of flexor digitorum brevis, the examiner and are attached to the dorsal digital expansions on their proximal passively extends the distal interphalangeal joint and asks the subject phalanges. to flex the toes at the proximal interphalangeal joint. Contracture of the tendons of flexor digitorum brevis can lead to toe deformities, and Relations The lumbricals are intimately related to the tendons of release or lengthening procedures may be required. The muscle belly is flexor digitorum longus before the latter enter their corresponding sometimes excised as a flap to cover a soft tissue defect. fibrous flexor sheaths. The lumbricals remain outside the fibrous flexor Abductor digiti minimi sheaths and cross the plantar aspects of the deep transverse metatarsal
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Attachments Abductor digiti minimi arises from both processes of ligaments before reaching the dorsal digital expansions. the calcaneal tuberosity, from the plantar surface of the bone between them, from the plantar aponeurosis and from the intermuscular septum Actions The lumbricals help to maintain extension of the interphalan­ between the muscle and flexor digitorum brevis. Its tendon glides in a geal joints of the toes. In injuries of the tibial nerve, and in conditions smooth groove on the plantar surface of the base of the fifth metatarsal such as the hereditary motor–sensory neuropathies (e.g. Charcot– and is attached, with flexor digiti minimi brevis, to the lateral side of Marie–Tooth disease), lumbrical dysfunction contributes to clawing of the base of the proximal phalanx of the fifth toe; hence it is more a the toes. flexor than an abductor. Some of the fibres arising from the lateral calcaneal process usually reach the tip of the tuberosity of the fifth Plantar muscles of the foot: third layer metatarsal (see Fig. 84.5B) and may form a separate muscle: abductor ossis metatarsi digiti quinti. An accessory slip from the base of the fifth The third layer of the foot contains the shorter intrinsic muscles of the metatarsal is not infrequent. toes, i.e. flexor hallucis brevis, adductor hallucis and flexor digiti minimi brevis (Fig. 84.22). Relations Abductor digiti minimi lies along the lateral border of the foot, and its medial margin is related to the lateral plantar vessels and Flexor hallucis brevis nerve (see Fig. 84.21). Attachments Flexor hallucis brevis has a bifurcate tendon of origin (see Figs 84.20, 84.22). The lateral limb arises from the medial part of Actions Despite its name, abductor digiti minimi is more a flexor than the plantar surface of the cuboid, posterior to the groove for the tendon an abductor of the metatarsophalangeal joint of the fifth toe. of fibularis longus, and from the adjacent part of the lateral cuneiform. The medial limb has a deep attachment directly continuous with the
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Plantar muscles of the foot: second layer lateral division of the tendon of tibialis posterior, and a more superficial attachment to the middle band of the medial intermuscular septum. The second layer consists of flexor accessorius and the four lumbrical The belly of the muscle divides into medial and lateral parts, the twin muscles. The tendons of flexor hallucis longus and flexor digitorum tendons of which are attached to the sides of the base of the proximal longus run in the same plane as the muscles of the second layer (see phalanx of the great toe. The medial part blends with the tendon of Fig. 84.20B); flexor hallucis longus and flexor digitorum longus are abductor hallucis, and the lateral with that of adductor hallucis, as they described on pages 1410–1412. reach their terminations.
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Muscles 1443 48 RETPAHC is no phalangeal attachment for the transverse part of the muscle; fibres that fail to reach the lateral sesamoid bone are attached with the oblique Tendons of part. flexor digitorum longus The transverse part of adductor hallucis is sometimes absent; part of the muscle may be attached to the first metatarsal, constituting an Tendon of opponens hallucis; a slip may also extend to the proximal phalanx of flexor hallucis longus the second toe. Tendons of Relations Adductor hallucis lies plantar to the metatarsal shafts and flexor digitorum brevis interossei and the long and short toe flexors. The medial and lateral plantar arteries and nerves are superficial, and flexor hallucis brevis is proximal and medial. Lumbricals Actions Adductor hallucis partly flexes the proximal phalanx of the great toe, but also stabilizes the metatarsal heads. Transverse Adductor head Third dorsal hallucis Oblique head interosseus Clinical anatomy Adductor hallucis is one of the deforming forces Second and third in hallux valgus and needs to be released during a distal soft tissue plantar interossei release when there is a fixed deformity. Flexor hallucis brevis Fourth dorsal interosseus Opponens digiti Flexor digiti minimi brevis minimi Attachments Flexor digiti minimi brevis arises from the medial part Abductor hallucis Flexor digiti minimi brevis of the plantar surface of the base of the fifth metatarsal, and from the Tendon of sheath of fibularis longus (see Figs 84.20B, 84.22 and 84.19A). It has Abductor digiti minimi flexor hallucis longus a distal tendon that inserts into the lateral side of the base of the proxi­ Tendon of fibularis longus Tendon of mal phalanx of the fifth toe; this tendon usually blends laterally with flexor digitorum that of abductor digiti minimi. Occasionally, some of its deeper fibres longus Flexor accessorius extend to the lateral part of the distal half of the fifth metatarsal, con­
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Tendon of tibialis posterior stituting what may be described as a distinct muscle: opponens digiti Flexor retinaculum Long plantar ligament minimi. Tendon of flexor hallucis longus Abductor digiti minimi Relations The fifth metatarsal shaft lies on the deep surface of flexor Plantar aponeurosis digiti minimi brevis, the interossei lie medially and abductor digiti Abductor hallucis minimi is lateral. The most lateral branch of the lateral plantar nerve Flexor digitorum brevis lies superficially and just medial to flexor digiti minimi brevis. Actions Flexor digiti minimi brevis flexes the metatarsophalangeal joint of the fifth toe. Fig. 84.22 Muscles of the sole of the foot, third layer. (With permission from Waschke J, Paulsen F (eds), Sobotta Atlas of Human Anatomy, 15th Plantar muscles of the foot: fourth layer ed, Elsevier, Urban & Fischer. Copyright 2013.) The fourth layer of muscles of the foot consists of the plantar and dorsal interossei and the tendons of tibialis posterior and fibularis longus A sesamoid bone usually occurs in each tendon near its attachment. (tibialis posterior and fibularis longus are described in Ch. 83). The Clinical problems with flexor hallucis brevis are usually related to the interossei resemble their counterparts in the hand except that, when associated sesamoid bones. However, excision of both sesamoid bones describing adduction and abduction of the toes, the axis of reference is leads to disruption of both tendons and a subsequent extension deform­ a longitudinal axis corresponding to the shaft of the second metatarsal ity at the first metatarsophalangeal joint; such surgery is, therefore, not (unlike in the hand, where reference is made to the long axis of the recommended. third metacarpal). Accessory slips may arise proximally from the calcaneus or long Dorsal interossei plantar ligament. A tendinous slip may extend to the proximal phalanx of the second toe. Attachments The dorsal interossei (Fig. 84.23A; see Fig. 84.19A) are
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situated between the metatarsals. They consist of four bipennate Relations Flexor hallucis brevis lies on the underside of the first muscles, each arising by two heads from the sides of the adjacent meta­ metatarsal shaft; abductor hallucis lies medially. The medial digital tarsals. Their tendons are attached to the bases of the proximal phalanges nerve to the great toe and the tendon of flexor hallucis longus pass to and to the dorsal digital expansions. The first inserts into the medial the great toe on its plantar surface. The medial plantar nerve lies more side of the second toe; the other three pass to the lateral sides of the superficially on its lateral side. second, third and fourth toes. Actions Flexor hallucis brevis flexes the proximal phalanx of the great Relations Between the heads of each of the three lateral muscles, there toe. is an angular space through which a perforating artery passes to the dorsum of the foot. Between the heads of the first muscle, the corres­ Testing The individual is asked to flex the first metatarsophalangeal ponding space transmits the terminal part of the dorsalis pedis artery joint with the interphalangeal joint extended, thereby eliminating the to the sole (see Fig. 84.1). action of flexor hallucis longus. Actions Dorsal interossei abduct the toes relative to the longitudinal Adductor hallucis axis of the second metatarsal. They also flex the metatarsophalangeal Attachments Adductor hallucis arises by oblique and transverse joints and extend the interphalangeal joints of the lateral four toes. The heads (see Figs 84.20B, 84.22 and 84.19A). The oblique head arises great and fifth toes have their own abductors. from the bases of the second, third and fourth metatarsals, and from the fibrous sheath of the tendon of fibularis longus. The transverse head Clinical anatomy Denervation of the interossei leads to claw­toe – a narrow, flat fasciculus – arises from the plantar metatarsophalangeal deformities. Development of clawed toes should alert the clinician to
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ligaments of the third, fourth and fifth toes (sometimes only from the the possibility of a neuropathic process (e.g. Charcot–Marie–Tooth third and fourth), and from the deep transverse metatarsal ligaments disease, tethered spinal cord). between them. The oblique head has medial and lateral parts. The medial part blends with the lateral part of flexor hallucis brevis and is Plantar interossei attached to the lateral sesamoid bone of the great toe. The lateral part There are three plantar interossei (see Fig. 84.23B). They lie below, joins the transverse head and is also attached to the lateral sesamoid rather than between, the metatarsals, and each is connected to only one bone and directly to the base of the first phalanx of the great toe. There metatarsal. They are unipennate, unlike the dorsal interossei; they arise
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AnklE And fooT 1444 9 noITCES The muscle belly and tendon of extensor hallucis brevis serve as guides A B to the location of the dorsalis pedis artery and deep fibular nerve. The tendon of extensor hallucis brevis can be used as a local graft. Vascular supply to the intrinsic muscles of the foot Abductor hallucis is supplied by the medial malleolar network, medial calcaneal branches of the lateral plantar artery (see Fig. 84.9), the medial plantar artery (directly and via superficial and deep branches), the first plantar metatarsal artery and perforators from the plantar art­ erial arch. Flexor digitorum brevis is supplied by the lateral and medial plantar arteries, the plantar metatarsal arteries and the plantar digital arteries to the lateral four toes. Abductor digiti minimi is supplied by the medial and lateral plantar arteries (see Figs 84.21, 84.25A), the plantar digital artery to the lateral side of this muscle, branches from 1st the deep plantar arch, the fourth plantar metatarsal artery, and end twigs from the arcuate and lateral tarsal arteries (see Fig. 84.9). Flexor 2nd 1st 2nd accessorius is supplied by the stem of the medial plantar artery (to the 3rd 3rd medial head), the lateral plantar artery and the deep plantar arch. The 4th lumbricals are supplied by the lateral plantar artery and deep plantar arch and by four plantar metatarsal arteries (four distal perforating arteries joined by three proximal perforating arteries). Their tendons are supplied by twigs from the dorsal digital arteries (and their parent dorsal metatarsal arteries) to the lateral four toes. Flexor hallucis brevis is supplied by branches of the medial plantar artery, the first plantar metatarsal artery, the lateral plantar artery and the deep plantar arch. Fig. 84.23 The interossei of the left foot. A, The dorsal interossei viewed Adductor hallucis is supplied by branches of the medial and lateral from the dorsal aspect. B, The plantar interossei viewed from the plantar plantar arteries, the deep plantar arch and the first to fourth plantar
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aspect. The axis to which the movements of abduction and adduction are metatarsal arteries. Flexor digiti minimi brevis is supplied by end twigs referred is indicated. of the arcuate and lateral tarsal arteries, and the lateral plantar artery and its digital (plantar) branch to the lateral side of the fifth toe. Dorsal interossei are supplied by the arcuate artery, lateral and medial tarsal from the bases and medial sides of the third, fourth and fifth metatar­ arteries, the first to fourth plantar arteries and the first to fourth dorsal sals, and insert into the medial sides of the bases of the proximal metatarsal arteries (receiving proximal and distal perforating arteries), phalanges of the numerically corresponding toes, and into their dorsal and by the dorsal digital arteries of the lateral four toes. Plantar inter­ digital expansions. ossei are supplied by the lateral plantar artery, the deep plantar arch, Relations The plantar interossei lie plantar to the dorsal interossei the second to fourth plantar metatarsal arteries and the dorsal digital and deep to the muscles of the third layer. arteries of the lateral three toes. Extensor digitorum brevis is supplied by the anterior perforating branch of the fibular artery, the anterior Actions Plantar interossei adduct the third, fourth and fifth toes, flex lateral malleolar artery, lateral tarsal arteries, dorsalis pedis artery, the metatarsophalangeal joints and extend the interphalangeal joints. arcuate artery, the first, second and third dorsal metatarsal arteries, proximal and distal perforating arteries, and the dorsal digital arteries Clinical anatomy The clinical anatomy of the plantar interossei is to the medial four toes (including the great toe). similar to that of the dorsal interossei. Innervation of the intrinsic muscles of the foot Abductor Extensor muscles of the foot hallucis is innervated by the medial plantar nerve, S1 and S2. Contrac­ tion of the muscle confirms an intact medial plantar nerve when the Extensor digitorum brevis and extensor integrity of this nerve is in question. Flexor digitorum brevis is innervated by the medial plantar nerve, hallucis brevis S1 and S2. Abductor digiti minimi and flexor accessorius are innervated
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Attachments Extensor digitorum brevis (see Fig. 84.2A) is a thin by the lateral plantar nerve, S1, S2 and S3. The first lumbrical is supplied muscle that arises from the distal part of the superolateral surface of by the medial plantar nerve; the other lumbricals are supplied by the the calcaneus in front of the shallow lateral groove for fibularis brevis, deep branch of the lateral plantar nerve, S2 and S3. Flexor hallucis from the interosseous talocalcaneal ligament, and from the deep surface brevis is supplied by the medial plantar nerve, S1 and S2. Adductor of the stem of the inferior extensor retinaculum. It slants distally and hallucis is innervated by the deep branch of the lateral plantar nerve, medially across the dorsum of the foot and ends in four tendons. The S2 and S3. Flexor digiti minimi brevis is innervated by the superficial medial part of the muscle is usually a more or less distinct slip, ending branch of the lateral plantar nerve, S2 and S3. Dorsal interossei are in a tendon that crosses the dorsalis pedis artery superficially to insert supplied by the deep branch of the lateral plantar nerve (S2 and S3), into the dorsal aspect of the base of the proximal phalanx of the great except that of the fourth intermetatarsal space, which is supplied by the toe; this slip is termed extensor hallucis brevis. The other three tendons superficial branch of the lateral plantar nerve. Plantar interossei are attach to the lateral sides of the tendons of extensor digitorum longus supplied by the deep branch of the lateral plantar nerve (S2 and S3), for the second, third and fourth toes. except that of the fourth intermetatarsal space, which is supplied by the The muscle is subject to much variation, e.g. accessory slips from the superficial branch of the lateral plantar nerve. Extensor digitorum brevis talus and navicular, an extra tendon to the fifth digit, or an absence of is supplied by the lateral terminal branch of the deep fibular nerve, L5
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one or more tendons. It may be connected to the adjacent dorsal and S1. interossei. Relations The most medial tendon, that of extensor hallucis brevis, VASCULAR SUPPLY courses dorsomedially and passes superficial to the dorsalis pedis artery and the deep fibular nerve. The remaining three tendons pass obliquely ARTERIES deep to the corresponding tendons of extensor digitorum longus. Dorsalis pedis artery Actions The muscle assists in extending the phalanges of the middle three toes via the tendons of extensor digitorum longus; for the great toe, it assists in extension of the metatarsophalangeal joint. The dorsalis pedis artery (see Fig. 84.1; Fig. 84.24) is usually the con­ tinuation of the anterior tibial artery distal to the ankle. It passes to the Clinical anatomy Laceration of extensor digitorum brevis leads to proximal end of the first intermetatarsal space, where it turns into little in the way of functional impairment because the long extensors the sole between the heads of the first dorsal interosseous to complete can compensate for the loss of the muscle. The proximal part of the the deep plantar arch, and provides the first plantar metatarsal artery. muscle can be used as interposition material to prevent bone fusion The artery may be larger than normal, to compensate for a small after resection of a calcaneonavicular bar (a common tarsal coalition). lateral plantar artery. It may be absent, in which event it is replaced by
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Vascular supply 1445 48 RETPAHC First dorsal metatarsal artery The first dorsal metatarsal artery (see Fig. 84.24) arises just before the dorsalis pedis artery enters the sole. It runs distally on the first dorsal interosseous and divides at the Anterior tibial artery cleft between the first and second toes. One branch passes under the tendon of extensor hallucis longus and supplies the medial side of the great toe; the other bifurcates to supply the adjoining sides of the great and second toes. Anterior medial Perforating branch of Cutaneous vessels from the dorsalis pedis artery The dor­ malleolar artery fibular artery salis pedis artery and its first dorsal metatarsal branch give rise to small Anterior lateral direct cutaneous branches that supply the dorsal foot skin between the malleolar artery extensor retinaculum and the first web space. This vessel provides the Dorsalis pedis artery Lateral basis for a fasciocutaneous flap raised from this region, and which may tarsal artery be used to cover superficial defects elsewhere. Deep plantar arch Medial tarsal arteries Arcuate artery The deep plantar arch (Fig. 84.25B) is deeply situated, extending from the fifth metatarsal base to the proximal end of the first intermetatarsal space. Convex distally, it is plantar to the bases of the second to fourth metatarsals and corresponding interossei, but dorsal to the oblique part of adductor hallucis. Branches Dorsal metatarsal arteries The deep plantar arch gives rise to three perforating and four plantar metatarsal branches, and numerous branches that supply the skin, fasciae and muscles in the sole. Three perforating branches ascend through the proximal ends of the second to fourth intermetatarsal spaces, between the heads of dorsal interossei, and anastomose with the dorsal metatarsal arteries. Four plantar metatarsal arteries extend distally between the metatarsals in contact with the interossei (Fig. 84.25). Each divides into two plantar digital arteries, supplying the adjacent digital aspects. Near its division, each plantar metatarsal artery sends a distal Dorsal digital
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perforating branch dorsally to join a dorsal metatarsal artery. The first arteries plantar metatarsal artery springs from the junction between the lateral plantar and dorsalis pedis arteries, and sends a digital branch to the Fig. 84.24 The dorsal arteries of the foot. medial side of the great toe. The lateral digital branch for the fifth toe arises directly from the lateral plantar artery near the fifth metatarsal base. Haemorrhage from the deep plantar arch is difficult to control because of the depth of the vessel and its important close relations. a large perforating branch of the fibular artery. It often diverges laterally from its usual route. Surface anatomy The lateral plantar artery begins between the heel and medial malleolus, Relations and crosses obliquely to a point 2.5 cm medial to the tuberosity of the The dorsalis pedis artery crosses, successively, the talocrural articular fifth metatarsal. With a slight distal convexity, it reaches the proximal capsule, talus, navicular and intermediate cuneiform and their liga­ end of the first intermetatarsal space. ments; superficial to it are the skin, fasciae, inferior extensor retinacu­ lum and, near its termination, extensor hallucis brevis. Medial to it is Posterior tibial artery the tendon of extensor hallucis longus and lateral to it are the medial tendon of extensor digitorum longus and medial terminal branch of Before the posterior tibial artery divides into its two main terminal the deep fibular nerve. The tendons are useful landmarks in the plan­ branches, it gives off a communicating branch that runs posteriorly ning of safe anatomical approaches in surgery of the ankle and foot. across the tibia approximately 5 cm above its distal end, deep to flexor Branches hallucis longus, and joins a communicating branch of the fibular artery; calcaneal branches, which arise just proximal to the termination of the The dorsalis pedis artery gives rise to the tarsal, arcuate and first dorsal posterior tibial artery, pierce the flexor retinaculum and supply the skin metatarsal arteries (see Figs 84.1, 84.9, 84.24).
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and fat behind the calcaneal tendon; and the artery of the tarsal canal. Tarsal arteries There are two tarsal arteries, lateral and medial (see The terminal branches of the posterior tibial artery are the medial and lateral plantar arteries. Fig. 84.24). They arise as the dorsalis pedis artery crosses the navicular. The lateral runs laterally under extensor digitorum brevis; it supplies Branches this muscle and the tarsal articulations, and anastomoses with branches Medial plantar artery The medial plantar artery is the smaller ter­ of the arcuate, anterior lateral malleolar and lateral plantar arteries, and minal branch of the posterior tibial artery (see Fig. 84.25). It arises the perforating branch of the fibular artery. Two or three medial tarsal midway between the medial malleolus and the medial calcaneal tuber­ arteries ramify on the medial border of the foot and join the medial cle, and passes distally along the medial side of the foot, with the medial malleolar arterial network. plantar nerve lateral to it. At first deep to abductor hallucis, it runs dis­ tally between abductor hallucis and flexor digitorum brevis, supplying Arcuate artery The arcuate artery (see Fig. 84.24) arises near the both. Near the first metatarsal base, when its calibre is already dimin­ medial cuneiform, passes laterally over the metatarsal bases, deep to ished as a result of supplying numerous muscular branches, it is further the tendons of the digital extensors, and anastomoses with the lateral diminished by a superficial stem. It passes to the medial border of the tarsal and plantar arteries. It supplies the second to fourth dorsal meta­ great toe, where it anastomoses with a branch of the first plantar meta­ tarsal arteries, running distally superficial to the corresponding dorsal tarsal artery. Its superficial stem then trifurcates and supplies three super­ interossei, and divides into two dorsal digital branches for the adjoining ficial digital branches that accompany the digital branches of the medial toes in the interdigital clefts. Proximally, these branches receive proxi­
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plantar nerve and join the first to third plantar metatarsal arteries. mal perforating branches from the deep plantar arch. Distally, they are joined by distal perforating branches from the plantar metatarsal arter­ Lateral plantar artery The lateral plantar artery is the larger termi­ ies. The fourth dorsal metatarsal artery sends a branch to the lateral side nal branch of the posterior tibial artery (see Fig. 84.25). It passes distally of the fifth toe. and laterally to the fifth metatarsal base; the lateral plantar nerve is The frequency of the arcuate artery has been reported to range from medial. The plantar nerves lie between the plantar arteries. Turning 10% to 67%, depending on the precise definition of the artery (DiLan­ medially, with the deep branch of the nerve, it gains the interval between dro et al 2001). the first and second metatarsal bases, and unites with the dorsalis pedis
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AnklE And fooT 1446 9 noITCES A B Plantar digital arteries Adductor hallucis, tendon of Plantar digital arteries oblique head Abductor hallucis Tendon of flexor hallucis brevis, lateral part Adductor hallucis, transverse head Dorsalis pedis artery, junction with deep plantar arch Plantar metatarsal arteries Digital branch to fifth toe Flexor hallucis brevis Deep plantar arch Superficial digital branch Medial plantar artery Lateral plantar artery Medial plantar artery Adductor hallucis, oblique head Flexor digitorum brevis Cutaneous branch Lateral plantar artery Abductor digiti minimi Flexor accessorius Abductor hallucis Abductor digiti minimi Calcaneal branches Flexor digitorum brevis Plantar aponeurosis Abductor hallucis Fig. 84.25 The plantar arteries of the left foot. A, Superficial dissection. B, Deep dissection. artery to complete the deep plantar arch. As it passes laterally, it is first The principal named superficial veins are the long and short saphen­ between the calcaneus and abductor hallucis, then between flexor digi­ ous. Their numerous tributaries are mostly (but not wholly) unnamed; torum brevis and flexor accessorius. Running distally to the fifth meta­ named vessels will be noted (see Fig. 78.9). As in the upper limb, the tarsal base, it passes between flexor digitorum brevis and abductor digiti vessels will be described centripetally from peripheral to major drainage minimi, and is covered by the plantar aponeurosis, superficial fascia channels. and skin. Dorsal digital veins receive rami from the plantar digital veins in the Muscular branches supply the adjoining muscles. Superficial clefts between the toes and then join to form dorsal metatarsal veins, branches emerge along the intermuscular septum to supply the skin which are united across the proximal parts of the metatarsals in a dorsal and subcutaneous tissue over the lateral part of the sole. Anastomotic venous arch. Proximal to this arch, an irregular dorsal venous network
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branches run to the lateral border and join branches of the lateral tarsal receives tributaries from deep veins and is continuous proximally with and arcuate arteries. Sometimes, a calcaneal branch pierces abductor a venous network in the leg. At each side of the foot, this network con­ hallucis to supply the skin of the heel. Anastomosis between the medial nects with medial and lateral marginal veins, which are both formed and lateral plantar arteries superficial to the flexor digitorum brevis is mainly by veins from more superficial parts of the sole. In the sole, sometimes present and is termed the superficial plantar arch. superficial veins form a plantar cutaneous arch across the roots of the toes and also drain into the medial and lateral marginal veins. Proximal Perforator flaps in the ankle and foot region to the deep plantar arch there is a plantar cutaneous venous plexus, especially dense in the fat of the heel. It connects with the plantar cutaneous venous arch and other deep veins, but drains mainly into the The arteries around the ankle and in the foot are the medial and lateral marginal veins. The veins of the sole are an important part of the lower calcaneal arteries, medial and lateral plantar arteries and the dorsalis limb ‘venous pump’ system aiding propulsion of blood up the limb pedis artery (see Fig. 78.7). In the foot, the two plantar arteries with (Broderick et al 2008). Intermittent foot compression devices are avail­ communicating arteries from the dorsalis pedis artery give rise to mul­ able to enhance this flow and so reduce the risk of deep vein thrombosis tiple small perfor ators. In the sole of the foot, the perforators emerge during periods of increased risk, e.g. after surgery. on either side of the plantar aponeurosis, and also pass through it, to supply the skin. ‘Island flaps’ from these perforators may be advanced to reconstruct small defects in the weight­bearing area. The skin of the INNERVATION sole of the foot is highly specialized and therefore, ideally, defects in this region should be reconstructed using local skin. Superficial fibular nerve DEEP AND SUPERFICIAL VENOUS SYSTEMS The superficial fibular nerve is described on page 1416. IN THE FOOT Deep fibular nerve
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Plantar digital veins arise from plexuses in the plantar regions of the toes. They connect with dorsal digital veins to form four plantar meta­ The deep fibular nerve is described on page 1416. tarsal veins, which run proximally in the intermetatarsal spaces and Tibial nerve connect via perforating veins with dorsal veins, then continue to form the deep plantar venous arch, which is situated alongside the deep plantar arterial arch. From this venous arch, medial and lateral plantar The branches of the tibial nerve that innervate structures in the ankle veins run near the corresponding arteries and, after communicating and foot are articular, muscular, sural, medial calcaneal and medial and with the long and short saphenous veins, form the posterior tibial veins lateral plantar nerves. The course and distribution of the tibial nerve in behind the medial malleolus. the calf are described on page 1415.
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Biomechanics of standing, walking and running 1447 48 RETPAHC Medial calcaneal nerve Proper plantar digital arteries The medial calcaneal nerve arises from the tibial nerve and perforates Proper plantar digital nerves the flexor retinaculum to supply the skin of the heel and medial side of the sole. Medial plantar nerve The medial plantar nerve is the larger terminal division of the tibial nerve, and lies lateral to the medial plantar artery. From its origin under the flexor retinaculum, it passes deep to abductor hallucis, then appears between it and flexor digitorum brevis, gives off a medial proper digital Common plantar nerve to the great toe, and divides near the metatarsal bases into three digital nerves common plantar digital nerves (Fig. 84.26; see Fig. 84.21). Plantar metatarsal Cutaneous branches pierce the plantar aponeurosis between abduc­ arteries tor hallucis and flexor digitorum brevis to supply the skin of the sole of the foot. Muscular branches supply abductor hallucis, flexor digit­ orum brevis, flexor hallucis brevis and the first lumbrical. The first two arise near the origin of the nerve and enter the deep surfaces of the Lateral plantar nerve, muscles. The branch to flexor hallucis brevis is from the hallucal medial Medial plantar nerve superficial branch digital nerve, and that to the first lumbrical from the first common plantar digital nerve. Articular branches supply the joints of the tarsus and metatarsus. Three common plantar digital nerves pass between the slips of the plantar aponeurosis, each dividing into two proper digital branches. The first supplies adjacent sides of the great and second toes; the second Plantar aponeurosis supplies adjacent sides of the second and third toes; and the third sup­ plies adjacent sides of the third and fourth toes, and also connects with the lateral plantar nerve. The first gives a branch to the first lumbrical. Each proper digital nerve has cutaneous and articular branches: near the distal phalanges, a dorsal branch supplies structures around the Flexor retinaculum nail. Abductor hallucis, flexor hallucis brevis and the first lumbrical are Medial calcaneal branches
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all supplied by the medial plantar nerve. (tibial nerve) Medial plantar nerve Lateral plantar nerve Posterior tibial artery The lateral plantar nerve supplies the skin of the fifth toe, the lateral Lateral plantar nerve half of the fourth toe, and most of the deep muscles of the foot (see Fig. 84.21). It is located medial to the lateral plantar artery and courses anteriorly towards the tubercle of the fifth metatarsal. Next, it passes Fig. 84.26 The plantar digital nerves. (With permission from Waschke J, Paulsen F (eds), Sobotta Atlas of Human Anatomy, 15th ed, Elsevier, between flexor digitorum brevis and flexor accessorius, and ends Urban & Fischer. Copyright 2013.) between flexor digiti minimi brevis and abductor digiti minimi by dividing into superficial and deep branches. Before division, it supplies flexor accessorius and abductor digiti minimi, and gives rise to small branches that pierce the plantar aponeurosis to supply the skin of the nerve can be damaged in severe inversion injuries of the ankle, and the lateral part of the sole (see Fig. 84.26). The superficial branch splits into deep fibular nerve is sometimes compressed by osteophytes in the two common plantar digital nerves: the lateral supplies the lateral side region of the second tarsometatarsal joint. Sural nerve entrapment is of the fifth toe, flexor digiti minimi brevis and the two interossei in the usually not due to compression by fascial elements. Entrapment of the fourth intermetatarsal space; the medial connects with the third third common digital nerve as it passes deep to the intermetatarsal liga­ common plantar digital branch of the medial plantar nerve and divides ment of the third (or less commonly the second) web space can result into two to supply the adjoining sides of the fourth and fifth toes. The in a Morton’s neuroma, which is probably the most common form of deep branch accompanies the lateral plantar artery deep to the flexor nerve entrapment in the foot. tendons and adductor hallucis, and supplies the second to fourth lum­ bricals, adductor hallucis and all the interossei (except those of the
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fourth intermetatarsal space). Branches to the second and third lumbri­ ANATOMY OF THE TOENAILS cals pass distally deep to the transverse head of adductor hallucis, and travel around its distal border to reach them. See Video 84.1. NAIL STRUCTURE Nerve entrapment syndromes in the foot A toenail consists of a nail plate and unit (Dykyj 1989; pages 151–152). The toenail is commonly a site of several pathologies, including ony­ All nerves of the foot can be affected by entrapment, leading classically chomycosis and onychocryptosis (Jules 1989, Eekhof et al 2012). to a burning sensation in the distribution of that nerve. Tarsal tunnel syndrome is much less common than carpal tunnel syndrome. The BIOMECHANICS OF STANDING, WALKING flexor retinaculum may compress the tibial nerve or either of its AND RUNNING branches (medial and lateral plantar nerves); entrapment at this level is most commonly due to a space­occupying lesion, e.g. a ganglion, or to compression by either a leash of vessels or the deep fascia associated PLANES OF MOTION with abductor hallucis. Compression of the first branch of the lateral plantar nerve (Baxter’s nerve) by the deep fascia that covers abductor Much confusion surrounds the descriptive terms for movement in the hallucis has been implicated as a possible cause of chronic heel pain foot and ankle. Plantar flexion and dorsiflexion refer to movement in and of plantar fasciitis. (Plantar fasciitis, often caused by repetitive high­ the sagittal plane and occur principally, but not exclusively, at the ankle, impact injury to the foot, may be associated with pain, especially over metatarsophalangeal and interphalangeal joints. Inversion is tilting of the medial calcaneal process, which may be exacerbated by passive the plantar surface of the foot towards the midline, and eversion is ankle or great toe flexion.) The medial plantar nerve can be compressed tilting away from the midline. This is motion in the coronal plane and
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at the ‘knot of Henry’, which is the point where the tendon of flexor takes place principally in the talocalcaneal and transverse tarsal joints. hallucis longus crosses deep to the tendon of flexor digitorum longus, Adduction is movement of the foot towards the midline in the trans­ to reach its medial side in the sole of the foot. The superficial fibular verse plane; abduction is movement away from the midline. This
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48 RETPAHC Ankle and foot Patients with Morton’s neuroma usually present with a main com­ plaint of metatarsalgia. While there is no pathognomonic clinical test, diagnostic imaging coupled with clinical tests can provide convergent validity to help with diagnosis (Owens et al 2011). Two commonly used clinical tests are web­space tenderness and forefoot squeeze tests. The web­space tenderness test is performed by placing the side of the thumb into the third web space and pressing down. The forefoot squeeze test is performed by squeezing the forefoot from side to side while concur­ rently performing the web­space test. 1447.e1
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AnklE And fooT 1448 9 noITCES movement occurs at the transverse tarsal joints and, to a limited degree, force fluctuations have to be larger at higher speeds, to give the same the first tarsometatarsal and metatarsophalangeal joints. vertical movement in less time. Supination describes a three­dimensional movement and is a com­ Development of walking bination of adduction, inversion and plantar flexion. Pronation is the opposite motion, i.e. a combination of abduction, eversion and dorsi­ The average child sits at 6 months, crawls at 9 months, walks with flexion. Pronation and supination are usually better terms than eversion support at 12 months, and walks without support at 18 months. The and inversion, as the latter rarely occur in isolation and the former characteristic early gait matures rapidly and is similar to that of the describe the ‘compound’ motion that usually occurs. adult by 3 years. Some minor changes occur up to 7 years, which are Active movements occur at the ankle, talocalcaneonavicular and sub­ largely a reflection of neurological development but are also related to talar joints. Movements at the ankle joint are almost entirely restricted stature (Thomson & Volpe 2001). Early gait is jerky, unsteady and wide­ to dorsiflexion and plantar flexion, but slight rotation may occur in based. Initial ground contact varies, and heel–toe, whole foot and toe– plantar flexion. The ranges of movement at the talocalcaneonavicular heel are all possible. Generally, a plantar flexed posture is adopted, and subtalar joints are greater; inversion and eversion mainly occur which contrasts with the adult pattern. In adults, heel strike is accom­ here. panied by a straight knee, which then flexes. A child strikes the ground with a flexed knee, which is then extended in response to weight­ bearing, and a short time is spent in single­leg stance (Fig. 84.28). STANDING Maturation is associated with diminution of base width and increase in step length and velocity. The earliest changes are development of heel­strike, knee flexion during stance, and reciprocal upper limb swing. Humans are bipedal: we stand and walk with an erect trunk and knees
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that are almost straight. Moreover, we are plantigrade, i.e. we set the Running whole length of the foot down on the ground, whereas most medium to large mammals are digitigrade, i.e. they stand and walk on their toes, and ungulates stand on hooves on the tips of their toes. In the sagittal Walking involves dual­support phases, but in running each foot is on plane, body weight acts along a line that passes a few centimetres ant­ the ground for 40% (jogging) to 27% (sprinting) of the stride, so there erior to the tibiotalar joint, exerting a moment that must be balanced is an aerial phase – the ‘double­float’ phase – when neither foot is on by the plantar flexor muscles. the ground. The faster the subject runs, the shorter the stance phase; world­class sprinters spend approximately 22% of the gait cycle in stance. During each aerial phase, the body rises and then falls under PROPULSION gravity, which means that its height and potential energy are maximal in the middle of this phase and minimal at mid­stance, when, in marked contrast to walking, the knee of the supporting leg bends. The The contraction of tibialis posterior, gastrocnemius and soleus is the changes in muscle belly lengths are relatively slight during running. The chief factor responsible for propulsion in walking, running and muscles are acting as tensioners of the tendons; indeed, most of the jumping. The propulsive action of these calf muscles is enhanced by change of length is produced by the stretch and recoil of the tendons. arching of the foot and flexion of the toes. In walking, the weight on It has been estimated that, of the kinetic and potential energy lost and the foot is taken successively on the heel, lateral border and the first regained in each stance phase, 35% is stored temporarily as elastic strain metatarsophalangeal joint. The last part of the foot to leave the ground energy in the calcaneal tendon, and 17% in the ligaments of the arch is the anterior pillar of the medial longitudinal arch and the medial of the foot. Together, these springs approximately halve the work three toes. In the act of sprinting, the heel does not touch the ground,
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required from the muscles. but the point of take­off is still the anterior pillar of the medial longi­ The calcaneal tendon is the most important ‘spring’ in the leg. Most tudinal arch. As the heel leaves the ground, the toes gradually extend. runners strike the ground first with the heel, and the centre of pressure Extension, of the great toe particularly, tightens the plantar aponeurosis moves rapidly forwards to the distal heads of the metatarsals, where it and thus heightens the arch. At the same time, flexor hallucis longus remains for most of the stance phase. and flexor digitorum longus elongate, which increases their subsequent As in walking, the ground force acts more or less in line with the contraction. The extrinsic and intrinsic toe flexors increase the force of leg, so the body is decelerated and re­accelerated during each stance take­off by exerting force on the ground. The most important muscle phase. The stance phase starts with deceleration and absorption of in this respect is flexor hallucis longus, which is strongly assisted by the energy. Power is generated after stance phase reversal as the limb pushes intrinsic toe flexors. The lumbricals provide a balancing action to the up with the knee extending and foot plantar flexed, and this continues extrinsic flexors and prevent buckling of the toes during the toe­off in the swing phase as the limb is accelerated forwards. Once the limb phase of gait. is ahead of the trunk, the final phase of swing­phase absorption is initi­ ated, during which the limb is decelerated. Walking The ground force acts upwards on the metatarsal heads, and the calcaneal tendon pulls upwards on the calcaneus. The necessary balan­ In walking, each foot is on the ground (stance phase) for approximately cing reaction occurs at the ankle, where the tibia presses downwards on 60% of the stride, and off the ground (swing phase) for approximately the talus. Together, these three forces flatten the longitudinal arch of 40% (Fig. 84.27). Thus, single­support phases (one foot on the ground) the foot, forcing the ankle 10 mm nearer to the ground than it would
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alternate with double­support phases (two feet on the ground). The be if the foot were rigid. Mechanical tests on amputated feet have shown knee is straight at heel strike and remains nearly straight (10–30°) for that the foot is a reasonably good spring, giving an energy return of most of the stance phase of that leg, bending more only immediately nearly 80%. The plantar aponeurosis, long and short plantar ligaments before toe­off. During the swing phase, the knee flexes to a maximum and the plantar calcaneonavicular ligament are all involved in the of 60° at mid­swing. spring action; they are predominantly collagenous but presumably have Stance phase starts with ‘heel strike’. With the foot still planted in elastic properties similar to those of tendon. front of the body, ‘foot flat’ is reached, and becomes ‘mid­stance’ when the body comes to be directly above the planted foot. The heel then rises as the contralateral foot makes contact with the ground (the MOVEMENTS OF THE FOOT ‘double stance’ phase). The last event of stance is ‘toe­off’ when the ‘swing phase’ starts. Early in the stance phase, while it is ‘foot flat’ in With the foot on the ground, body weight causes some supination front of the trunk, the foot pushes downwards and forwards on the (used here to imply uneven distribution of weight to the lateral side of ground, decelerating the body as well as supporting it. Later, when the the foot) and flattening of the longitudinal arches; about one­third of foot is behind the trunk, it pushes downwards and backwards, the weight borne by the forefoot is taken by the head of the first meta­ re­accelerating the body (see Fig. 84.27). tarsal (McDonald and Tavener 1999). When a resting position becomes The height of the centre of gravity, and therefore the potential energy active, as occurs on starting to walk, the foot is pronated (used here to of the body, also fluctuates. This is inevitable if the knee is kept nearly imply uneven distribution of weight to the medial side of the foot) by fully extended, making the hip move in a near­circular arc about the muscular effort, and the first metatarsal is depressed (the second less
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ankle of the supporting foot. The vertical component of the total force so), which accentuates the longitudinal arch to its maximum height exerted by both feet on the ground in the double­support phase is (Hicks 1954). Similar changes can be imposed on a weight­bearing foot greater than body weight, giving the body an upward acceleration. The by active lateral rotation, which is transmitted through the tibia to the vertical component of the ground force during the single­support phase talus and entails passive supination of the foot. Medial rotation has an is less than body weight, giving the body a downward acceleration. The opposite effect. When the foot is grounded and immobile, muscles that
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Biomechanics of standing, walking and running 1449 48 RETPAHC Phase of gait Stance phase Swing phase Double Double support Single-limb support support Single-limb support (opposite side) Pressure Heel strike Foot flat Mid-stance Heel-off Toe-off Mid-swing Heel strike distribution Hip Joint angle (extension = 0º) 45º 40º 30º 20º 5º 0º 20º 40º 50º 45º Flexor mm Extensor mm Abductor mm Adductor mm Knee Joint angle (extension = 0º) 5º 10º 15º 10º 5º 10º 65º 55º 30º 5º Flexor mm Extensor mm Ankle foot Joint angle 5º 10º 0º 5º 5º 0º 5º 0º 5º 5º (neutral = 0º) plantar- plantar- dorsi- dorsi- plantar- plantar- plantar- Dorsiflexor mm Plantar flexor mm Inverter mm Everter mm Intrinsic mm Ground reaction force % Body weight 100 Vertical force 15 Deceleration 0 Acceleration –15 Sagittal force % Gait cycle 0 10 20 30 40 50 60 70 80 90 100 Fig. 84.27 The events that occur during the different phases of a normal gait cycle. Depicted are: distribution of pressure on the plantar surface of the foot; changes in the angles of hip, knee and ankle joints, together with activity in the corresponding muscle groups; and vertical and horizontal (sagittal plane) components of the ground reaction force during stance phase. (Chart collated from various sources by Michael Gunther, Department of Human Anatomy and Cell Biology, University of Liverpool.)
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AnklE And fooT 1450 9 noITCES A A B B C C Fig. 84.29 The concept of the foot skeleton as a twisted plate that may be untwisted (supination) or further twisted (pronation) during the maintenance of a plantigrade stance in various positions of the foot. A, The foot skeleton in supination, as in standing with the feet widely separated. Note the marked medial tilting of the talus and, to a lesser Fig. 84.28 Development of a mature gait. A, A 1-year-old. Note the flexed degree, of the calcaneus and the depression of the medial longitudinal elbows and lack of arm swing. The foot is plantar flexed at contact. B, A arch. B, Relative pronation of the foot, as in standing with the feet close 3-year-old. Arm swing is now present, as is heel strike. C, A 6-year-old. together. C, Supination of the foot when standing on an inclined surface; There is now an adult-type gait. (With permission from Benson MKD, if the position of the wedge had been reversed, the foot skeleton would, Fixsen JA, MacNicol MF (eds) 2001 Development of a mature gait. In: of course, approach maximal pronation. (Based on MacConaill MA 1945 Children’s Orthopaedics and Fractures, 2nd edn. Edinburgh: Churchill The postural mechanism of the human foot. Proc Roy Irish Acad Livingstone.) 50:265–278.) move it when it is freely suspended may exert effects on the leg, e.g. the dorsiflexors can then pull the leg forwards at the ankle joint. (though this varies with the position of the feet (Fig. 84.29), the devel­ The foot has two major functions: to support the body in standing opment of associated soft tissues, and the nature of the surface). In any and progression, and to lever it forwards and absorb shock in walking, activity, as soon as the heel rises, the toes are extended and muscular running and jumping (Alexander 1992). To fulfil the first function, the structures (including the plantar aponeurosis) tighten up in the sole,
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pedal platform must be able to spread the stresses of standing and accentuating the longitudinal arches. It has been suggested that tension moving, and be pliable enough to accommodate walking or running diminishes in the deeper plantar ligaments in this phase. over uneven and sloping surfaces. To fulfil the second function, the foot The sole is transversely concave, both in skeletal form and usually must be transformable into a strong, adjustable lever in order to resist in external appearance, and serial transverse arches are most developed inertia and powerful thrust; a segmented lever can best meet such inferior to the metatarsus and adjoining tarsus. Transmission of force stresses if it is arched. occurs at the metatarsal heads, to some degree along the lateral border In infants and young children, fatty connective tissue on the plantar of the foot, and through subjacent soft tissues. aspect may give the foot a flat appearance and soft tissues modify its In standing, with only body weight to support, both the intrinsic appearance to varying degrees at all ages. The thickness of the medial and extrinsic muscles appear to relax (Perry 2010). If the longitudinal mid­foot plantar fat pad ranges from 3.1 to 4.9 mm (Riddiford­Harland arches are allowed to sink as a result of muscular relaxation, the plantar et al 2007). However, the skeleton of the human foot is normally ligaments tie the bones into an arched form. The medial arch is more arched, and the sole of the foot is usually visibly concave. These arches elevated when the feet are together than when they are apart, i.e. inver­ vary individually in height, especially the longitudinal in its medial sion with supination increases as the feet are separated. This medial sag part. Since they are dynamic, their heights also differ in different phases can be countered by voluntary contraction of muscles such as tibialis of activity. anterior. Pronation and supination ensure that in standing, whatever The medial longitudinal arch contains the calcaneus, talus, navicular, the position of the feet, a maximal weight­bearing area is grounded, cuneiform and medial three metatarsals. Its summit, at the superior from the metatarsal heads along the lateral border of the foot to the
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talar articular surface, takes the full thrust from the tibia and passes it calcaneus. The twist of the ligamentous skeleton of the foot imparted backwards to the calcaneus, and forwards through the navicular and by pronation (which is partly undone in supination) prompts the liken­ cuneiforms to the metatarsals. When the foot is grounded, these forces ing of the foot to a twisted but resilient plate (see Fig. 84.29), where are transmitted through the three metatarsal heads and calcaneus (espe­ adequate ground contact was ensured whatever the angle between the cially its tuberosity). The medial arch is higher, and more mobile and foot and leg, and adaptable resilience was imparted in standing and resilient than the lateral arch; its flattening progressively tightens the progression. plantar calcaneonavicular ligament and plantar aponeurosis. The lateral arch is adapted to transmit weight and thrust rather than to absorb such Bonus e-book images and video forces; the long plantar and plantar calcaneocuboid ligaments tighten as it flattens. The lateral arch makes contact with the ground more extensively than the medial arch. As the foot flattens, an increasing fraction of load Fig. 84.19 Turbo spin-echo, T1-weighted magnetic resonance (MR) traverses soft tissues, which are inferior to the entire arch. The whole images of the left ankle of a woman aged 26. lateral border usually touches the ground, whereas the medial border does not. However, the medial border is visibly concave, usually even Video 84.1 Ankle block: surface anatomy. in standing, which explains the familiar outline of human footprints
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1451 48 RETPAHC key references KEY REFERENCES Barclay­Smith EB 1896 Astragalo­calcaneo­navicular joint. J Anat 30: Eekhof JA, Van Wijk B, Knuistingh Neven A et al 2012 Interventions for 390–412. ingrowing toenails. Cochrane Database Syst Rev 4:CD001541. The first description of the astragalo-calcaneo-navicular joint and explained A meta-analysis of the efficacy of procedures used to treat ingrown toenails. the importance of the joint complex in terms of hindfoot motion. Jones FW 1949 Structure and Function as Seen in the Foot, 2nd ed. London: Chen TM, Rozen WM, Pan WR et al 2009 The arterial anatomy of the Achil­ Baillière, Tindall & Cox. les tendon: anatomical study and clinical implications. Clin Anat 22: Remains one of the classic texts on the foot. 377–85. Kim PJ, Richey JM, Wissman LR et al 2010 The variability of the Achilles A demonstration that the calcaneal tendon has three main territories of tendon insertion: a cadaveric examination. J Foot Ankle Surg 49: vascularity: a proximal section, mid-section and distal section. The 417–20. mid-section had the poorest blood supply of all three territories. A description of the variability in the terminal insertion site of the calcaneal DiLandro AC, Lilja EC, Lepore FL et al 2001 The prevalence of the arcuate tendon that may be dependent on age. artery: a cadaveric study of 72 feet. J Am Podiatr Med Assoc 91: Wildenauer E 1950 Die Blutversorgung des Talus. Zeitschrift für Anatomie 300–5. und Entwicklungsgeschichte 115:32–6. A large cadaveric study in which the authors found that the arcuate artery The first comprehensive account of talar blood supply and the identification was present in only 16.7% of their sample of feet. They established that the of the important artery of the tarsal canal. lateral tarsal artery supplied dorsal metatarsal arteries 2–4 in 47.2% of their sample, an arrangement that was more frequently found than the
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commonly described arcuate artery.
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48 RETPAHC Ankle and foot REFERENCES Ahmed IM, Lagopoulos M, McConnell P et al 1998 Blood supply of the Dykyj D 1989 Anatomy of the nail. Clin Podiatr Med Surg 6:215–28. Achilles tendon. J Orthop Res 16:591–6. Eekhof JA, Van Wijk B, Knuistingh Neven A et al 2012 Interventions for Alexander R McN 1992 The Human Machine. New York: Columbia Univer­ ingrowing toenails. Cochrane Database Syst Rev 4:CD001541. sity Press. A meta-analysis of the efficacy of procedures used to treat ingrown toenails. Barclay­Smith EB 1896 Astragalo­calcaneo­navicular joint. J Anat 30: Gardner E, Gray DJ 1968 The innervation of the joints of the foot. Anat Rec 390–412. 161:141–8. A paper that gave the first description of the astragalo-calcaneo-navicular Gluck GS, Heckman DS, Parekh SG 2010 Tendon disorders of the foot and joint and explained the importance of the joint complex in terms of hindfoot ankle, part 3: the posterior tibial tendon. Am J Sports Med 38: motion. 2133–44. Barnes DJ 2003 Anatomy of the Lower Extremity. Marietta, OH: CBLS. Gregersen HN 1977 Naviculocuneiform coalition. J Bone Joint Surg Am Blouet JM, Rebaud C, Marquer Y et al 1983 Anatomy of the tarsometatarsal 59:128–30. joint and its applications to dislocation of this articular interface. Anat Gupta SC, Gupta CD, Arora AK 1977 Pattern of talar articular facets in Clin 5:9–16. Indian calcanei. J Anat 124:651–5. Bonnel F, Teissier P, Colombier JA et al 2013 Biometry of the calcaneocuboid Halvorson JJ, Winter SB, Teasdall RD et al 2012 Talar neck fractures: a sys­
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joint: biomechanical implications. Foot Ankle Surg 2013:70–5. tematic review of the literature. J Foot Ankle Surg 52:56–61. Bonnel F, Teissier P, Maestro M et al 2011 Biometry of bone components in Harris RI 1965 Retrospect–personeal (sic) spastic flat foot (rigid valgus foot). the talonavicular joint: a cadaver study. Orthop Traumatol Surg Res: J Bone Joint Surg Am 47:1657–67. S66–73. Harris RI, Beath T 1948 Etiology of peroneal spastic flat foot. J Bone Joint Boss AP, Hintermann B 2002 Anatomical study of the medial ankle ligament Surg Br 30B:624–34. complex. Foot Ankle Int 23:547–53. Hicks JH 1954 The mechanics of the foot. II. The plantar aponeurosis and Brennan SA, Kiernan C, Maleki F et al 2012 Talonavicular synostosis with the arch. J Anat 88:25–30. lateral ankle instability – a case report and review of the literature. Foot Hopkinson WJ, St Pierre P, Ryan JB et al 1990 Syndesmosis sprains of the Ankle Surg 18:e34–e36. ankle. Foot Ankle 10:325–30. Broderick BJ, Corley GJ, Quondamatteo F et al 2008 A haemodynamic study Jennings MM, Christensen JC 2008 The effects of sectioning the spring liga­ of the physiological mechanisms of the venous pump in the healthy ment on rearfoot stability and posterior tibial tendon efficiency. J Foot human foot. Conf Proc IEEE Eng Med Biol Soc:1411–14. Ankle Surg 47:219–24. Carmont MR, Rees RJ, Blundell CM 2009 Freiberg’s disease. Foot Ankle Int Johnson KA, Strom DE 1989 Tibialis posterior tendon dysfunction. Clin 30:167–76. Orthop Relat Res 239:196–206. Carr AJ, Norris SH 1989 The blood supply of the calcaneal tendon. J Bone Jones FW 1949 Structure and Function as Seen in the Foot, 2nd ed. London:
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Joint Surg Br 71:100–1. Baillière, Tindall & Cox. Castro M, Melao L, Canella C et al 2010 Lisfranc joint ligamentous complex: Remains one of the classic texts on the foot. MRI with anatomic correlation in cadavers. Am J Roentgenol 195: W447–55. Jules KT 1989 Nail infections. Clin Podiatr Med Surg 6:403–16. Cavazos GJ, Khan KH, D’Antoni AV et al 2009 Cryosurgery for the treatment Kapandji IA 2011 The Physiology of the Joints, 6th ed. Edinburgh: Elsevier, of heel pain. Foot Ankle Int 30:500–5. Churchill Livingstone. Cerrato RA 2011 Freiberg’s disease. Foot Ankle Clin 16:647–58. Kim PJ, Martin E, Ballehr L et al 2011 Variability of insertion of the Achilles tendon on the calcaneus: an MRI study of younger subjects. J Foot Ankle Chaney DM 2010 The Lisfranc joint. Clin Podiatr Med Surg 27:547–60. Surg 50:41–3. Chang HW, Lin CJ, Kuo LC et al 2012 Three­dimensional measurement of Kim PJ, Richey JM, Wissman LR et al 2010 The variability of the Achilles foot arch in preschool children. Biomed Eng Online 11:76. tendon insertion: a cadaveric examination. J Foot Ankle Surg 49: Chen TM, Rozen WM, Pan WR et al 2009 The arterial anatomy of the Achil­ 417–20. les tendon: anatomical study and clinical implications. Clin Anat A description of the variability in the terminal insertion site of the calcaneal 22:377–85. tendon that may be dependent on age. A demonstration that the calcaneal tendon has three main territories of vascularity: a proximal section, mid-section and distal section. The Kose O 2010 Do we really need radiographic assessment for the diagnosis mid-section had the poorest blood supply of all three territories. of non­specific heel pain (calcaneal apophysitis) in children? Skeletal Radiol 39:359–61.
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Coskun N, Yuksel M, Cevener M et al 2009 Incidence of accessory ossicles Landorf KB, Menz HB 2008 Plantar heel pain and fasciitis. Clin Evid and sesamoid bones in the feet: a radiographic study of the Turkish (Online). PMID: 19450330; PMCID: PMC2907928. subjects. Surg Radiol Anat 31:19–24. League AC 2008 Current concepts review: plantar fasciitis. Foot Ankle Int Cummins EJ, Anson BJ 1946 The structure of the calcaneal tendon (of Achil­ 29:358–66. les) in relation to orthopedic surgery, with additional observations on the plantaris muscle. Surg Gynecol Obstet 83:107–16. Lemley F, Berlet G, Hill K et al 2006 Current concepts review: tarsal coalition. Foot Ankle Int 27:1163–9. Daftary A, Haims AH, Baumgaertner MR 2005 Fractures of the calcaneus: a review with emphasis on CT. RadioGraphics 25:1215–26. Lemont H, Ammirati KM, Usen N 2003 Plantar fasciitis: a degenerative process (fasciosis) without inflammation. J Am Podiatr Med Assoc Davis WH, Sobel M, DiCarlo EF et al 1996 Gross, histological, and micro­ 93:234–7. vascular anatomy and biomechanical testing of the spring ligament complex. Foot Ankle Int 17:95–102. Lohrer H, Arentz S, Nauck T et al 2008 The Achilles tendon insertion is crescent­shaped: an in vitro anatomic investigation. Clin Orthop Relat Deland JT 2008 Adult­acquired flatfoot deformity. J Am Acad Orthop Surg Res 466:2230–7. 16:399–406. McDonald SW, Tavener G 1999 Pronation and supination of the foot: con­ de Palma L, Santucci A, Sabetta SP et al 1997 Anatomy of the Lisfranc joint fused terminology. Foot 9:6–11. complex. Foot Ankle Int 18:356–64.
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Michaud TC 2011 Human Locomotion: The Conservative Management of DiLandro AC, Lilja EC, Lepore FL et al 2001 The prevalence of the arcuate Gait­Related Disorders. Newton, MA: Newton Biomechanics. artery: a cadaveric study of 72 feet. J Am Podiatr Med Assoc 91: 300–5. Micheli LJ, Ireland ML 1987 Prevention and management of calcaneal apo­ A large cadaveric study in which the authors found that the arcuate artery physitis in children: an overuse syndrome. J Pediatr Orthop 7:34–8. was present in only 16.7% of their sample of feet. They established that the Milner CE, Soames RW 1998 The medial collateral ligaments of the human lateral tarsal artery supplied dorsal metatarsal arteries 2–4 in 47.2% of ankle joint: anatomical variations. Foot Ankle Int 19:289–92. their sample, an arrangement that was more frequently found than the Muehleman C, Williams J, Bareither ML 2009 A radiologic and histologic commonly described arcuate artery. study of the os peroneum: prevalence, morphology, and relationship to Durrant B, Chockalingam N, Hashmi F 2011 Posterior tibial tendon dysfunc­ degenerative joint disease of the foot and ankle in a cadaveric sample. tion: a review. J Am Podiatr Med Assoc 101:176–86. Clin Anat 22:747–54. 1451.e1
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9 noITCES AnklE And fooT Myerson MS 1997 Adult acquired flatfoot deformity: treatment of dysfunc­ Scheyerer MJ, Helfet DL, Wirth S 2011 Diagnostics in suspicion of ankle tion of the posterior tibial tendon. Instr Course Lect 46:393–405. syndesmotic injury. Am J Orthop (Belle Mead NJ) 40:192–7. Nakai T, Takakura Y, Tanaka Y 2000 Morphologic changes of the ankle in Snow SW, Bohne WH, DiCarlo E 1995 Anatomy of the Achilles tendon and children as assessed by radiography and arthrography. J Orthop Sci plantar fascia in relation to the calcaneus in various age groups. Foot 5:134–8. Ankle Int 16:418–21. Owens R, Gougoulias N, Guthrie H et al 2011 Morton’s neuroma: clinical Subhas N, Vinson EN, Cothran RL et al 2008 MRI appearance of surgically testing and imaging in 76 feet, compared to a control group. Foot Ankle proven abnormal accessory anterior­inferior tibiofibular ligament (Bas­ Surg 17:197–200. sett’s ligament). Skeletal Radiol 37:27–33. Oyedele O, Maseko C, Mkasi N et al 2006 High incidence of the os pero­ Takigawa M 1953 Study upon strength of human and animal tendons. neum in a cadaver sample in Johannesburg, South Africa: possible J Kyoto Pref Med Univ 53:915–33. clinical implications? Clin Anat 19:605–10. Thomson P, Volpe RG 2001 Introduction to Podopediatrics, 2 ed. Edin­ Panchani PN, Chappell TM, Moore GD et al 2014 Anatomic study of the burgh: Elsevier, Churchill Livingstone. deltoid ligament of the ankle. Foot Ankle Int 35:916–21. Trepal MJ, Cangiano SA, Anarella JJ 1986 Transchondral fractures of the talar A large cadaveric study in which the authors studied the morphology and dome. J Foot Surg 25:369–73. variations of the bands that comprise the deltoid ligament. They reported
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Varner KE, Michelson JD 2000 Tarsal coalition in adults. Foot Ankle Int that the ligament can be composed of up to 8 different bands. 21:669–72. Pankovich AM, Shivaram MS 1979 Anatomical basis of variability in injuries Wildenauer E 1950 Die Blutversorgung des Talus. Zeitschrift für Anatomie of the medial malleolus and the deltoid ligament. I. Anatomical studies. und Entwicklungsgeschichte 115:32–6. Acta Orthop Scand 50:217–23. The first comprehensive account of talar blood supply and the identification Perry J 2010 Gait Analysis: Normal and Pathological Function, 2nd ed. of the important artery of the tarsal canal. Thorofare, NJ: SLACK. Yamada H 1970 Strength of Biological Materials. Huntington, NY: Robert E. Rachel JN, Williams JB, Sawyer JR et al 2011 Is radiographic evaluation neces­ Krieger. sary in children with a clinical diagnosis of calcaneal apophysitis (sever Yepes H, Tang M, Geddes C et al 2010 Digital vascular mapping of the disease)? J Pediatr Orthop 31:548–50. integument about the Achilles tendon. J Bone Joint Surg Am 92: Riddiford­Harland DL, Steele JR, Baur LA 2007 The use of ultrasound 1215–220. imaging to measure midfoot plantar fat pad thickness in children. Yi TI, Lee GE, Seo IS et al 2011 Clinical characteristics of the causes of plantar J Orthop Sports Phys Ther 37:644–7. heel pain. Ann Rehabil Med 35(4):507–13. Ryan JD, Timpano ED, Brosky TA 2nd 2012 Average depth of tarsometatarsal Zantop T, Tillmann B, Petersen W 2003 Quantitative assessment of blood joint for trephine arthrodesis. J Foot Ankle Surg 51:168–71. vessels of the human Achilles tendon: an immunohistochemical cadaver Salmon M, Taylor GI, Razaboni RM 1994 Anatomic Studies: Arteries of the study. Arch Orthop Trauma Surg 123:501–4.
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Muscles of the Extremities and the Trunk: Arterial Anastomotic Path­ Zaw H, Calder JD 2010 Tarsal coalitions. Foot Ankle Clin 15:349–64. ways of the Extremities. St Louis: Quality Medical Publishers. Sarrafian SK 2011 Anatomy of the Foot and Ankle: Descriptive, Topographic, Functional, 3rd ed. Philadelphia: Lippincott Williams & Wilkins. 1451.e2
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COMMENTARY 9.1 Nerve biomechanics Although assumed postures and movements place physical forces on tive tissue fibres contribute to stiffness (Borschel et al 2003). Endoneur­ peripheral nerves, the biomechanical properties of these nerves permit ial fluid and the perineurial sheath that maintains the fluid compartment continued electrical signalling in the face of reasonable physical also contribute to stiffness. When a nerve is elongated, it undergoes demands. Consider the sciatic nerve in an individual moving from a transverse contraction (Walbeehm et al 2004): the reduction in cross­ standing to a seated posture. Where it crosses the lateral rotators of the sectional area increases endoneurial compartment pressure contribut­ femur, the nerve undergoes lengthening, its cross­sectional shape ing to nerve stiffness (Millesi et al 1995). As one might predict, nerve becomes elliptical and narrowed, and endoneurial fluid is forced proxi­ roots, which lack a perineurial sheath, demonstrate less stiffness than mally and distally away from the site of shape change. The segment of a peripheral nerve (Beel et al 1986). External features, such as nerve the sciatic nerve in the thigh glides proximally, converging towards the branching and entering/exiting blood vessels, resist elongation of a flexing hip joint and diverging away from the flexing knee joint (Topp nerve in its nerve bed, and increase nerve stiffness measured in situ and Boyd 2006). (Millesi et al 1995). When a nerve bed is elongated across a moving joint, the nerve undergoes longitudinal tension. The biomechanical response of that nerve may be documented in a load–elongation curve, in which load is measured in Newtons and length in millimetres (Haftek 1970). To enable comparisons to be made between nerves, it is helpful to measure their cross­sectional areas and starting lengths, and translate the load– elongation curves into stress–strain curves. Stress is defined as the inten­ sity of force per unit cross­sectional area, and may be reported in N/m2 or MPa (Pascal). Strain is defined as the ratio of change in length to the o ler nig gi tn ha . l Tl hen reg et h d, isa tn ind c ti s r
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eo gf it oen n sr e ap reo r st ee ed n a s in a lop ae drc –e en lt oa ng ge a o tif o nth e o ro sr tig rein ssa –l Stiffness s tit ora ni n o fc u verv rye s l i( tF tli eg l. o 9 a. d1 . o1 r) . s tI rn e st sh e re i sn ui lt ti sa l i n‘t o sie g’ n r ie fig cio ann t o ef l oth ne g ac tu iorv ne , o a rp sp trl aic ina­ . Slope = In the ‘linear behaviour’ region, there is a correlation between the applied tensile load or stress and the elongation or strain. In the ‘plastic’ region of the curve, minimal tensile load or stress results in mechanical Toe region failure and discontinuity of nerve structures. Several structural features of peripheral nerves may be related to segments of the stress–strain curve. Nerve in situ is under tension; the transition between the ‘toe’ region and the ‘linear behaviour’ region of the curve corresponds roughly with the in situ strain (Kwan et al 1992). When severed, a peripheral nerve recoils approximately 10% of its length. The elasticity observed in the stress–strain curve is due to struc­ tures that make up visible, periodic light–dark bands that were initially described by, and named after, Felix Fontana (Fontana 1781). These bands vary in their angulation, width, spacing and periodicity; they have long been assumed to be optical artefacts produced by the char­ acteristic zig­zag course of individual nerve fibres (i.e. axons, both myelinated and unmyelinated) lying within the perineurial sheath. A strong linear relationship between increasing nerve strain and decreas­ ing band frequency and axonal undulations has been demonstrated experimentally in rat sciatic nerve using Fourier analysis (Love et al 2013). In vivo microdissection studies coupled with computer model­ ling suggest that the layers of perineurial cells are probably responsible
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for the short­wavelength, large­amplitude bands and that wavy spiral­ ling nerve fibres in the endoneurium are responsible for the long­ wavelength, small­amplitude bands (Merolli et al 2012), the two patterns merging to form the visible bands of Fontana. Interestingly, a recent study of Trembler-J mice, a model of Charcot–Marie–Tooth disease, suggested that the altered bands of Fontana in Trembler-J sciatic nerve appear to be the result of unusually long, sinuous axons moving Fig. 9.1.1 Typical load–elongation (A) and stress–strain curves (B) for a out of phase (Power et al 2015). The zig­zag, spiralling nerve fibres are peripheral nerve. The transition between the toe region and the linear thought to provide the elasticity evident in the ‘toe’ region of the stress– region in the stress–strain curve (asterisk) has been shown to correspond strain curve. Increasing strain in the ‘linear behaviour’ region of the approximately with the strain in situ. The slope of the stress–strain curve stress–strain curve causes the bands of Fontana to disappear (Pourmand is called the modulus of elasticity and represents the stiffness of the et al 1994). nerve, as seen in the load–elongation curve. If the slope is steep, then the Anatomical features have been studied to discern their contribution nerve has more stiffness and is less compliant to elongation. If the slope to the ‘linear behaviour’ region of the stress–strain curve. The slope of is less steep, then the nerve has less stiffness and is more compliant to this region is termed Young’s modulus of elasticity, or in the case of the elongation. Once the nerve has reached ultimate strain, the structural load–elongation curve, it indicates the stiffness of a nerve. A steep slope integrity of the nerve is overcome and the deformation is termed ‘plastic’ indicates that a nerve is stiff, and significant tensile force results in only or ‘permanent’. (From Topp KS, Boyd BS 2006 Structure and modest change in length. The modulus of elasticity or stiffness of an biomechanics of peripheral nerves: nerve responses to physical stresses
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e80 acellular nerve is similar to that of fresh nerve, indicating that connec­ and implications for physical therapist practice. Phys Ther 86:92–109.) )N( daoL Plastic region Ultimate load 12 1 680 Linear behaviour region Ultimate elongation 4 2 0 0 5 10 15 20 Elongation (mm) Plastic region Ultimate stress 12 1 680 Co inrr e ss itp uo sn td ras i nw *ith Linear behaviour region Modulus of elasticity U slt ti rm aa inte 4 Slope = 2 Toe region 0 0 5 10 15 20 25 30 35 40 45 Strain (%) )aPM( ssertS Kimberly S Topp A B
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Nerve biomechanics e81 1.9 YRATNEMMOC In the ‘plastic’ region of the stress–strain curve, increasing longitu­ increasing stress along the ‘linear behaviour’ region of the stress–strain dinal stress causes non­recoverable elongation and structural integrity curve, long before the ultimate strain is reached. is lost. The force per unit cross­sectional area at the point of mechanical Nerve is best described as a viscoelastic tissue because its biomech­ failure is termed ultimate stress and occurs at ultimate strain. At this anical properties are time­dependent. In response to fixed tension, point, a nerve behaves like a viscous material (Haftek 1970). Along the nerve demonstrates creep or elongation over time (Grewal et al 1996). stress–strain curve, structures within the nerve become impaired in a Slow elongation allows for higher ultimate strain (Haftek 1970, Rydevik hierarchical fashion. With increasing tensile load, there is first sliding et al 1990). When stretched to a fixed length, nerve exhibits stress and loss of tenuous connections in the interface between the layer of relaxation or a reduction in tension over time (Wall et al 1991, Driscoll inner perineurial cells and the sheath of outer perineurial cells and et al 2002). associated epineurial tissues (Tillett et al 2004, Georgeu et al 2005). Returning to the example of the sciatic nerve, during movement from With continued load, the core of nerve fibres and inner perineurial cell standing to seated, the nerve bed is elongated posterior to the hip as layers is disrupted and function is impaired or lost; ultimately, the forward trunk motion causes flexion at the hip joint. The sciatic nerve sheath of outer perineurial and epineurial tissues ruptures. Given that is exposed to tensile load or stress with resultant elongation or strain. acellular nerve demonstrates significantly lower tensile strength and Adjusting to these forces, segments of the nerve converge towards the ultimate strain than fresh nerve (Borschel et al 2003), the perineurial flexing hip joint, with minimal motion in distant segments (Topp and cell layer should be appreciated for its ability to withstand stress. Boyd 2006). Endoneurial pressure resists transverse contraction. When
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Although definitive anatomical studies are lacking, it is likely that the seated posture is assumed and maintained, the nerve undergoes microscopic disruptions of perineurial cell–cell connections occur with stress­relaxation – until the next postural adjustment. REFERENCES Beel JA, Stodieck LS, Luttges MW 1986 Structural properties of spinal nerve Merolli A, Mingarelli L, Rochchi L 2012 A more detailed mechanism to root: biomechanics. Exp Neurol 91:30–40. explain the ‘Bands of Fontana’ in peripheral nerves. Muscle Nerve 46: Borschel GH, Kia KF, Kuzon WM et al 2003 Mechanical properties of acel­ 540–7. lular peripheral nerve. J Surg Res 114:133–9. Millesi H, Zoch G, Reihsner R 1995 Mechanical properties of peripheral Driscoll PJ, Glasby MA, Lawson GM 2002 An in vivo study of peripheral nerves. Clin Orthop Relat Res 314:76–83. nerves in continuity: biomechanical and physiological responses to Pourmand R, Oches S, Jersild RA 1994 The relation of the beading of myeli­ elongation. J Orthop Res 20:370–5. nated nerve fibers to the bands of Fontana. Neuroscience 61:373–80. Fontana F 1781 Traité sur le vénin de la vipere, sur les poisons américains, Power BJ, O’Reilly G, Murphy R et al 2015 Normal nerve striations are sur le laurier­cerise et sur quelques autres poisons végetaux. On y a joint altered in the Trembler­J mouse, a model of Charcot–Marie–Tooth des observations sur la structure primitive du corps animal. Différentes disease. Muscle Nerve 51:246–52. experiences sur la reproduction des nerfs et la description d’un nouveau Rydevik BL, Kwan MK, Myers RR et al 1990 An in vitro mechanical and canal de l’œil, vol. 2. Florence: Nyon L’Ainè. histological study of acute stretching on rabbit tibial nerve. J Orthop Res Georgeu GA, Walbeehm ET, Tillett R et al 2005 Investigating the mechanical 8:694–701.
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shear­plane between core and sheath elements. Cell Tissue Res 320: Tillett RL, Afoke A, Hall SM et al 2004 Investigating mechanical behavior at 229–34. a core–sheath interface in peripheral nerve. J Peripheral Nerv Sys 9: Grewal R, Xu J, Sotereanos DG et al 1996 Biomechanical properties of 255–62. peripheral nerves. Hand Clin 12:195–204. Topp KS, Boyd BS 2006 Structure and biomechanics of peripheral nerves: Haftek J 1970 Stretch injury of peripheral nerve. Acute effects of stretching nerve responses to physical stresses and implications for physical thera­ on rabbit nerve. J Bone Joint Surg 52:354–65. pist practice. Phys Ther 86:92–109. Kwan MK, Wall EJ, Massie J et al 1992 Strain, stress and stretch of peripheral Walbeehm ET, Afoke A, de Wit T et al 2004 Mechanical functioning of nerve. Rabbit experiments in vitro and in vivo. Acta Orthop Scand 63: peripheral nerves: linkage with the ‘mushrooming’ effect. Cell Tissue Res 267–72. 316:115–21. Love JM, Chuang T­H, Lieber RL et al 2013 Nerve strain correlates with Wall EJ, Kwan MK, Rydevik BL et al 1991 Stress relaxation of a peripheral structural changes quantified by Fourier analysis. Muscle Nerve 48: nerve. J Hand Surg Am 16:859–63. 433–5.
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COMMENTARY Functional anatomy and biomechanics 9.2 of the pelvis Andry Vleeming, Frank H Willard This commentary focuses on the anatomy and biomechanics of the men and women (Vleeming et al 2012). The increase in mobility of the pelvic girdle and, specifically, the sacroiliac joints. In bipeds, the pelvis pelvic ring seen in the post-pubescent female pelvis is functional in serves as a basic platform with three large levers acting on it (the spine allowing passage for the child during labour. When the data are com- and two lower limbs). Movement of the pelvic platform upon the hip bined from published studies employing RSA and appropriate placing joints relative to the femur, such as flexion and extension (pelvic ante- of markers, the maximum sagittal rotation of the sacroiliac joint never and retroversion), and rotation and abduction/adduction, strongly exceeds 3.6° and translation of the joint never exceeds 2 mm (Kibsgård influences lumbar spinal movement. As well as this substantial exter- et al 2012). If these data are amalgamated with the observation that nal pelvic motion, internal pelvic motion through the sacroiliac joint osteophytosis is rare in women, regardless of age (1.83% of females), is essential for effectively transferring loads between the spine and and is not very common in men (12.27%; Dar et al 2008), it appears lower limbs. It has been postulated that the sacroiliac joints act as that small sacroiliac joint movements are present, even at an advanced important stress relievers in the ‘force–motion’ relationships between age (Vleeming et al 2012). the trunk and lower limb (Vleeming et al 2007). These joints ensure that the pelvic girdle is a flexible ring of bone that will not easily frac- Sacroiliac joint stability ture under the great forces to which it might be subject, either from trauma or from its many bipedal functions (Lovejoy 1988). Analysis of To illustrate the importance of both myofascial and ligamentous stabil- gait mechanics demonstrates that the sacroiliac joints provide suffi- ity of the sacroiliac joint, the biomechanical principles of form and
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cient flexibility for the intrapelvic forces to be transferred effectively to force closure were introduced (Vleeming et al 1990a, Vleeming et al and from the lumbar spine and lower extremities (Vleeming et al 1990b). Form closure refers to a theoretical stable situation in a joint 2007). with closely fitting surfaces, where no extra forces are needed to main- The sacroiliac joint is a highly specialized joint that lends stable (yet tain the state of the system. With force closure (leading to joint com- flexible) support to the upper body. Both the tightness of the well- pression), both a lateral force and friction are needed to withstand developed dorsal fibrous apparatus and the specific architecture of the vertical load. The structural features that contribute to sacroiliac joint sacroiliac joint result in limited mobility. Numerous researchers have form closure are complementary ridges and grooves of the articular tried to model sacroiliac joint function by studying its principal dis- surfaces; dorsocranial ‘wedging’ of the sacrum into the ilia; a particular placement characteristics. A common assumption of these studies is high coefficient of friction in the sacroiliac joint (Vleeming et al 1990a, that increased loading on the sacrum leads to tilting of the sacrum Vleeming et al 1990b); and the integrity of the dorsal binding ligaments ventrally (nutation), a process by which most dorsal sacroiliac joint in particular, which are among the strongest in the body (Vleeming et al ligaments are stretched and the dorsal aspects of the iliac bones are 1990a). Both form and force closure are necessary for balancing friction/ drawn together (Solonen 1957, Vleeming et al 1990a, Vleeming et al compression in the sacroiliac joint. Force closure is the result of altered 1990b). Counternutation normally takes place in unloaded situations, joint reaction forces by tensing ligaments, fasciae, muscles and ground such as lying. Nutation implies a forward tilting of the sacrum relative reaction forces (Vleeming et al 1990a, Vleeming et al 1990b). Force to a posterior rotation of the ilia, and vice versa in counternutation.
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closure ideally generates a perpendicular compressional reaction force to the sacroiliac joint to overcome the forces of gravity (Vleeming et al Sacroiliac joint movement 1990b). Pelvic motion of males and females has been investigated by roentgen Biomechanical considerations and the active stereophotogrammetric motion analysis (RSA). RSA is a technique for straight leg raise (ASLR) test in pelvic girdle measuring small movements and is regarded as the gold standard for pain (PGP) patients determining mobility in orthopaedics (Kibsgård et al 2012). Several studies applied this technique to measure the mean sacroiliac joint mobility, especially around the sagittal axis, in patients with pelvic PGP patients, who test positively on the functional ASLR test, show an girdle pain (PGP; Sturesson 2007). The average mobility for men is inability to raise the leg while lying supine. This test can temporarily about 40% less than for women. However, with age, there was no be normalized by manual anterior compression of the pelvis or the use detectable decrease in total mobility in either gender (in patients up to of a pelvic belt. This suggests that increased unilateral motion of the 50 years old). In fact, there was a significant increase of mobility with sacroiliac joint could lead to impairment and failure to lift the leg age for both moving from a ‘supine to sitting position’ and from ‘stand- (Mens et al 1999). ing to lying prone with hyperextension’ position, particularly in women. Likewise, Sturesson (2007), using RSA, studied the effects of surgical Likewise, gender differences of symphysial motion were analysed in a application of an anterior external fixation frame for severe PGP group of 45 asymptomatic individuals. In men, the average frontal patients. This resulted in a mean reduction of movement of the sacro- plane movement was 1.4 mm, and in nulliparous women 1.6 mm. iliac joint around the helical axis of 59% and around the X-axis of 74%. However, in multiparous women, motion increased to 3.1 mm (Garras In addition, the ASLR test and other evidence-based PGP tests were
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et al 2008). normalized (Vleeming et al 2008). When the frame was tightened, a The increased sacroiliac joint mobility in females compared to males nutation movement of the sacrum was noticed (Sturesson 2007). has possible anatomical correlates. The curvature of the sacroiliac joint This and other studies mentioned in this commentary imply that surfaces is usually less pronounced in women to allow for greater ‘too much movement’ of the sacroiliac joint could be a significant factor mobility (Vleeming et al 1990a). Also, the pubic angle differs between in the onset of PGP (Vleeming et al 2008). REFERENCES Dar G, Khamis S, Peleg S et al 2008 Sacroiliac joint fusion and the Garras DN, Carothers JT, Olson SA 2008 Single-leg-stance (flamingo) radio- implications for manual therapy diagnosis and treatment. Man Ther 13: graphs to assess pelvic instability: how much motion is normal? J Bone e82 155–8. Joint Surg Am 90:2114–18.
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Functional anatomy and biomechanics of the pelvis e83 2.9 YRATNEMMOC Kibsgård TJ, Røise O, Stuge B et al 2012 Precision and accuracy measurement Vleeming A, Volkers AC, Snijders CJ et al 1990b Relation between form and of radiostereometric analysis applied to movement of the sacroiliac function in the sacroiliac joint. Part II: Biomechanical aspects. Spine joint. Clin Orthop Relat Res 470:3187–94. 15:133–6. Lovejoy CO 1988 Evolution of human walking. Sci Am 25:118–25A. Vleeming A, Mooney V, Stoeckart R (eds) 2007 Movement, Stability and Mens JM, Vleeming A, Snijders CJ et al 1999 The active straight leg raising Lumbopelvic Pain: Integration of Research and Therapy, 2nd ed. Edin- test and mobility of the pelvic joints. Eur Spine J 8:468–73. burgh: Elsevier, Churchill Livingstone, p. 658. Solonen KA 1957 The sacroiliac joint in the light of anatomical, roentgeno- Vleeming A, Albert HB, Ostgaard HC et al 2008 European guidelines for the logical and clinical studies. Acta Orthop Scand 27:1–127. diagnosis and treatment of pelvic girdle pain. Eur Spine J 17:794–819. Sturesson B 2007 Movement of the sacroiliac joint with special reference Vleeming A, Schuenke MD, Masi AT et al 2012 The sacroiliac joint: an over- to the effect of load. In: Vleeming A, Mooney V, Stoeckart R (eds) view of its anatomy, function and potential clinical implications. J Anat Movement, Stability and Lumbopelvic Pain: Integration of Research 221:537–67. and Therapy, 2nd ed. Edinburgh: Elsevier, Churchill Livingstone, pp. 343–52. Vleeming A, Stoeckart R, Volkers AC et al 1990a Relation between form and function in the sacroiliac joint. Part I: Clinical anatomical aspects. Spine 15:130–2.
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COMMENTARY 9.3 Articularis genus Stephanie J Woodley Articularis genus, sometimes referred to as the ‘articular muscle of the capsule (DiDio et al 1967, Kimura and Takahashi 1987, Woodley et al knee’ (Puig et al 1996), is a small muscle located deep to vastus inter­ 2012, Reider et al 1981). The muscle may be triangular, rectangular or medius on the anterior aspect of the thigh (Fig. 9.3.1). Due to its distal trapezoid in shape (DiDio et al 1967, Toscano et al 2004, DiDio et al capsular insertions, it is morphologically similar to the subanconeus 1969). There is considerable variation in the reported mean muscle muscle (articularis cubiti) of the elbow joint, although subanconeus is length (between 6.2 and 14 cm in adults; Ahmad 1975, DiDio et al considered to represent the deep fibres of the medial head of triceps 1967, Toscano et al 2004, Woodley et al 2012), as well as the number brachii (rather than being a separate entity) and its function is likely to of constituent bundles, which typically ranges from 1 to 7 (Puig et al differ from that of articularis genus (Tubbs et al 2006). From an evolu­ 1996, Ahmad 1975, DiDio et al 1967, Toscano et al 2004, Sakuma et al tionary perspective, fibres corresponding to articularis genus have been 2014) but sometimes exceeds 10 (DiDio et al 1969, Reider et al 1981; described in early tetrapods (Diogo and Molnar 2014) and it is compar­ see Table 9.3.1). The number of bundles may be underestimated when able to the subcrureus muscle of primates including apes, gorillas and viewed using magnetic resonance imaging (Puig et al 1996, Woodley
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lemurs (Murie and Mivart 1872, Hepburn 1892). A distinct, yet small, et al 2012), possibly because of the reasonably compact nature of this articularis genus is also found in domestic animals such as the dog, cat muscle. Recent dissection evidence demonstrates that 6 of 11 different and goat (Getty 1975, Kincaid et al 1996, Glenn and Samojla 2002, muscle bundles, organized in superficial, intermediate and deep layers, Evans 2013). are consistently present (Woodley et al 2012; Fig. 9.3.4). The superficial While articularis genus has been of interest to anatomists for over layer usually comprises a large central bundle bordered by lateral and two centuries (refer to DiDio et al (1967) for a historical account), medial bundles; fascicles in some of these bundles may insert into the controversy still surrounds many aspects of its architecture. Discrepan­ bursa through an intermediary thin areolar membrane (see Fig. 9.3.4). cies in the literature are most likely to be the result of differences in A central bundle forms the intermediate layer, and two bundles (medial study methodologies, particularly with respect to the type and scope of and lateral) make up the deepest part of articularis genus, and may be data collected and/or in definitions of the muscle and its components. accompanied by a third, central bundle (Sakuma et al 2014). Bundle To date, most studies of articularis genus have been dissection­based; there are only three studies in which modern imaging techniques have been used to investigate morphology (Puig et al 1996, Roth et al 2004, Woodley et al 2012) (Table 9.3.1). Ant Articularis genus consists of staggered layers of bundles (Puig et al Sup Inf 1996, Kimura and Takahashi 1987, Woodley et al 2012) that arise from Post the distal third of the anterior, medial and lateral surfaces of the femur (Ahmad 1975, DiDio et al 1967, Woodley et al 2012, DiDio et al 1969) (Fig. 9.3.2), with a broad attachment to the proximal and/or posterior
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margins of the suprapatellar bursa (Puig et al 1996, Ahmad 1975, Kimura and Takahashi 1987, Toscano et al 2004, Woodley et al 2012, S VI I D Sakuma et al 2014) (Fig. 9.3.3) and specific regions of the articular Fig. 9.3.2 A medial view of the bundles of articularis genus arranged into superficial (S), intermediate (I) and deep (D) layers, inserting into the suprapatellar bursa. Note that some superficial fascicles insert into the Fig. 9.3.1 An anterior deep surface of the vastus intermedius (VI) tendon. view of the thigh showing articularis genus (AG) deep to the reflected vastus intermedius (VI) muscle. VI Other abbreviations: AG N, nerve branch to VI articularis genus from the femoral nerve; AG P, proximal border * N of bisected patella; VM, vastus medialis; * midpoint of suprapatellar bursa. * VM P Fig. 9.3.3 A sagittal proton density MRI scan of the knee from a Sup Med Lat 23-year-old female. The distal portion of articularis genus (AG), deep to e84 Inf vastus intermedius (VI), is seen inserting into the suprapatellar bursa (*).
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Articularis genus e85 3.9 YRATNEMMOC Table 9.3.1 Summary of data relating to the morphology of articularis genus Study Study characteristics (type, General muscle morphology; origin and insertion Architectural parameters specimen number and sex) DiDio et al Dissection following injection of Separated from VI by connective tissue and fat Muscle length: mean 8 cm (range 3–13 cm) (1967) gelatine Shape: rectangular 56%; trapezoid 27%; inverted trapezoid 17% Most proximal point of insertion: mean 10.5 cm (range 8–16 cm)a n = 156 adults O: distal femur, anterior, medial and lateral Bundles: n = 1–6, most commonly 1 or 2 (78%); same number bilaterally in 104 male, 52 female I: articular capsule at the level of the suprapatellar bursa, mostly 60% of individuals proximal, centre. Also to medial and lateral aspects, Maximum bundle width: mean 0.9 cm (range 0.1–4.0 cm) occasionally anterior and posterior DiDio et al Dissection Shape: triangular 44%; lambdoidal 27%; rectangular 24%; Muscle length (fetal, n = 14): mean 4.4 cm; range 1.2–5.4 cm (1969) n = 66 (fetuses, newborn, adults) unclassified 5% Maximum muscle width (fetal, n = 14): mean 0.9 cm; range 0.2–2.0 cm Histology O: distal third of femur, anterior (92.4%) and lateral or medial Bundles: n = 1, 66.7%; n = 2 divergent but not separate, 27.3%; n = 2, 1.5%; n = 16 fetuses aspects (30.3%) unaccounted, 4.5%. Same number bilaterally in 82% of individuals 29–34 weeks I: articular capsule at the level of the suprapatellar bursa Ahmad Dissection Margins demarcated by fat and connective tissue Muscle length: mean 9 cm
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(1975) n = 20 O: distal femur, usually anterior, occasionally medial and lateral Fibre direction: mostly vertical, some inferomedial or inferolateral aspects Bundles: n = 1–2 most common, sometimes 3–4 I: suprapatellar bursa, proximal border. Central, medial or lateral, Innervation: branch of nerve to VI occasionally posterior or anterior aspects Reider et al Dissection Flat and wispy without distinct investing fascia Muscle width: range 1.5–3 cm (1981) n = 24 from 48 adults O: anterior aspect supracondylar portion of femur 26 male, 22 femaleb I: joint capsule at suprapatellar bursa 40–90 years Kimura and Dissection Superficial and deep layers, separated by fat Most proximal point of insertionc: range 14.9–16.5 cm (superficial layer); Takahashi n = 44 adults Superficial layer: derived from lower muscle bundles of VI 10.2–11.9 cm (deep layer) (1987) 36 male, 8 femaleb I: suprapatellar bursa, posterior aspect, spreading medially and Bundles: n = >10 bundles laterally. Posterior aspect of capsule Deep layer: mean 3.4 bundles; range 1–7, usually 2 Superficial layer: 2 bundles Bundle length: range 5.2–6.6 cm (superficial layer); 3.5–5.0 cm (deep layer) Innervation: femoral nerve, one branch derived from the common branch to VI and VL, the other from that to VM and VI (superficial layer). Deep layer supplied by common branch to VM and VI Puig et al MRI (prospective and retrospective) O: anterior surface of femur Maximal muscle transverse aread: mean 1.2 ± 0.3 cm2; range 0.8–2.0 cm2 (1996) n = 40 from 34 patients I: suprapatellar bursa, proximal surface, medial and lateral aspect Highest point of insertiona: mean 6.4 ± 0.5 cm; range 3.5–9.0 cm
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19 male, 15 femaleb of posterior surface Bundles: n = mean 2.4 ± 0.7; range 1–4 16–56 years Most proximal bundle: mean length 4.7 ± 0.4 cm; range 3.1–6.6 cm; mean anglee 11.4 ± 1.3°; range 6.0–17.5°; mean transverse diameter (at origin) 0.9 ± 0.08 cm; range 0.6–1.3 cm Most distal bundle: mean length 2.8 ± 0.4 cm; range 0.9–3.5 cm; mean anglee 12.4 ± 2.5°; range 5.0–20.0° Roth et al MRI (retrospective) Anteroposterior muscle thickness: range 0.1–0.8 cm (2004) 92 knees from 84 patients 42 male, 42 female 20–76 years Toscano et al Dissection Separated from VI by fat of variable thickness Muscle length: mean 6.2 cm; range 3.8–8.5 cm (2004) n = 65 from 44 adults Shape: trapezoid 40%; rectangular 33%; triangular and irregular Most distal point of insertionf: mean 3.0 cm; range 2.0–4.1 cm 36 male, 8 femaleb 27% Bundles: n = range 2–7, 4 most frequent (33%) O: distal third of femur, usually anterior (43%) Bundle orientation: mostly vertical, some oblique I: suprapatellar bursa, often anterior (57%) Woodley et al MRI and dissection Distinct from VI Muscle lengthh: mean 13.9 ± 1.1 cm; 12.3–17.4 cm (2012)g n = 18 adults Staggered arrangement comprised of three layers (superficial, Muscle PCSA: mean 1.5 ± 0.7 cm2; range 0.5–3.3 cm2 8 male, 10 female intermediate and deep)
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71–97 years O: distal 32% of femur (range 29–42 cm), anterior, anterolateral Fascicle length: mean 5.9 ± 1.0 cm Histology or anteromedial surfaces Bundles: n = mean 7 ± 1.8; range 4–10, same number bilaterally in 44% of n = 4 adults I: proximal and/or posterior wall of suprapatellar bursa, directly or individuals; MRI mean 3.8 ± 0.8; range 2–5, significantly less than 4 male via a thin areolar membrane; deep surface of distal tendon of dissection (p <0.0001) 68–80 years VI (superficial bundles); knee joint capsule, posterior or Bundle orientation: mostly vertical (1–5°) except three bundles (two of posteromedial surface (one intermediate and both deep which were in deep layer; mean range 11–15°) bundles) Most proximal point of insertiona: mean 12.4 ± 2.9 cm; range 7.2–17.4 cm Most distal point of insertiona: mean 3.3 ± 2.8 cm; range 0–10.4 cm Fibre type: inconclusive due to variation Sakuma et al Dissection Superficial and deep layers, separated by fat in some All measurements relate to deep layer (2014) n = 40 from 22 adults Deep layer comprised of three bundles (medial, central, lateral) Bundles: n = 2.7 ± 0.5 13 male, 9 female O: anterior aspect of femur Bundle length: mean 5.4 ± 1.3 cm; medial bundle longer than lateral 77–98 years I: Junction of suprapatellar bursa and joint cavity proper (deep (p < 0.05) fibres) Bundle areai: 5.5 ± 2.6 cm2; medial bundle larger than lateral (p < 0.05) and central (p < 0.05) bundles aProximal border or apex of patella used as landmark. bRepresents number of cadavers/participants, not specimens. cRelative to the distal end of the medial femoral condyle, unclear if data from one specimen or all specimens.
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dIn this study ‘±’ refers to SEM. eAngle recorded between anterior surface of femur and posterior surface of muscle bundle. fRelative to superior edge of trochlea. gAll data relate to dissection measures unless stated. hIn this study ‘±’ refers to standard deviation. iCalculated by multiplying bundle length by width. Abbreviations: I, insertion; MRI, magnetic resonance imaging; n, number; O, origin; PCSA, physiological cross-sectional area; VI, vastus intermedius; VL, vastus lateralis; VM, vastus medialis. orientation is predominantly longitudinal, although the deepest two it is possible that this arrangement enables the longer, superficial fasci­ peripheral bundles may be oriented obliquely (Puig et al 1996, cles to accommodate changes in muscle length (Woodley et al 2012), Ahmad 1975, Toscano et al 2004, Woodley et al 2012). Symmetry of particularly during knee flexion, where it is postulated that the length bundle arrangement in the right and left limbs of individuals appears of each bundle of articularis genus elongates two­fold at the end­range variable (40–82%; DiDio et al 1967, Woodley et al 2012, DiDio et al of movement (Kimura and Takahashi 1987). 1969, Sakuma et al 2014). There has been long­standing debate as to whether articularis genus Articularis genus is diminutive: its mean physiological cross­sectional is a deep bundle of quadriceps femoris or an independent muscle area of 1.5 ± 0.7 cm2 (cadaver specimens; Woodley et al 2012) indicates (DiDio et al 1967). While it is true that articularis genus and vastus that it is capable of generating only a small amount of force. Fascicle intermedius share an innervation from branches of the femoral nerve length (mean 5.9 ± 1.0 cm; Woodley et al 2012) is likely to be influ­ (Ahmad 1975, Kimura and Takahashi 1987; see Fig. 9.3.1), other ana­
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enced by bundle location (Puig et al 1996, Kimura and Takahashi 1987, tomical data tend to favour the view that articularis genus is an inde­ Woodley et al 2012). The deepest, most distal layer of articularis genus pendent muscle. First, although a small percentage of superficial contains the shortest fascicles, and the superficial, proximal bundles fascicles in the superficial bundles of articularis genus may insert into contain the longest (Woodley et al 2012; see Fig. 9.3.4). Functionally, the deep layer of the distal tendon of vastus intermedius (see Fig. 9.3.2),
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ARTiCulARis gENus e86 9 NOiTCEs the bulk of articularis genus appears distinct from the overlying quad­ riceps (Kimura and Takahashi 1987, Woodley et al 2012). Second, the two muscles may be delineated by a distinct fascial layer of variable composition and thickness (Ahmad 1975, DiDio et al 1967, Toscano et al 2004), although this feature is inconsistent (Kimura and Takahashi 1987, Woodley et al 2012, Toscano et al 2004). The fibre type profiles, albeit limited to four cadaver specimens, appear to differ between artic­ ularis genus and vastus intermedius (Woodley et al 2012). Perhaps the most reliable method of defining articularis genus is by reference to its A discrete distal insertion sites into the suprapatellar bursa and/or joint capsule (Kimura and Takahashi 1987, Woodley et al 2012). Articularis P VI * AM S genus may hypertrophy (Puig et al 1996) or atrophy (Toscano et al * S 2004) in parallel with quadriceps femoris, but the significance of these adaptations is unknown. When contemplating function, the architectural arrangement of articularis genus is paramount because direct evidence regarding its action is limited to a single study (Ahmad 1975). Ahmad observed elevation of the knee joint capsule and synovial membrane on stimulat­ ing a branch of the femoral nerve innervating articularis genus in three patients undergoing surgical amputation. This finding is consistent with previous hypotheses, suggesting that articularis genus is responsible for retracting the suprapatellar bursa or knee joint capsule proximally B (Ahmad 1975, DiDio et al 1967, Kimura and Takahashi 1987, Roth et al 2004, Toscano et al 2004), potentially preventing interposition of these structures between the patella and femur during extension of the S I S knee joint (Ahmad 1975, DiDio et al 1967). Functional implications may be elucidated from comparison with the dog stifle (knee) joint, P * D
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where articularis genus usually consists of two thin bundles (medial and lateral) forming an ‘inverted­V’ shaped muscle (Kincaid et al 1996), approximately 2 mm wide (Evans 2013). This morphology, together with the distribution of muscle spindles, which are located both in the vicinity of the muscle­capsule interface and isolated within the capsular connective tissue, suggest that in addition to tensioning the suprapatel­ lar bursa (Kincaid et al 1996, Evans 2013), articularis genus may have an important proprioceptive role (Kincaid et al 1996). A detailed knowledge of the morphology of articularis genus is rel­ C evant to understanding normal function of the knee joint as well as its Inf Sup role in possible dysfunction; for example, the possible protective role that articularis genus may have in counteracting impingement of cap­ D sular tissues (Ahmad 1975, DiDio et al 1967) might be appropriate to Fig. 9.3.4 The three layers of articularis genus. A, The superficial (S) layer, consider in some individuals who present with undifferentiated ant­ where some fascicles insert into the suprapatellar bursa via an areolar erior knee pain (Woodley et al 2012). It is perhaps surprising that this membrane (AM). Note the presence of a complete superior plica muscle has not been afforded more attention; given its complexity and (arrowheads), positioned between the knee joint cavity and the variability, there is scope for further examination of its detailed anatomy suprapatellar bursa. B, The intermediate (I) layer beneath the reflected and function, particularly in healthy volunteers. Techniques such as superficial (S) bundles. C, Two deep (D) bundles, positioned laterally and dynamic magnetic resonance imaging and electromyography may be medially. Other abbreviations: P, proximal pole of bisected patella; VI, useful adjuncts to morphological investigations, and assist in contribut­ vastus intermedius tendon; * proximal border of the midpoint of the ing to a better understanding of the functional and clinical relevance suprapatellar bursa. of this interesting muscle. REFERENCES
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Ahmad I 1975 Articular muscle of the knee – articularis genus. Bull Hosp Kincaid SA, Rumph F, Garrett PD et al 1996 Morphology of the musculus Joint Dis 36:58–60. articularis genus in dog with description of ectopic muscle spindles. DiDio LJ, Zappalá A, Carney WP 1967 Anatomico­functional aspects of the Anat Histol Embryol 25:113–16 + 6 pl. musculus articularis genus in man. Acta Anat (Basel) 67:1–23. Murie J, Mivart St G 1872 On the anatomy of the Lemuroidea. Trans Zool DiDio LJA, Zappalá A, Cardoso AD et al 1969 Muscularis articularis genus Soc Lond 7:1–113. in human fetuses, newborn and young individuals. Anat Anz 124: Puig S, Dupuy DE, Sarmiento A et al 1996 Articular muscle of the knee: a 121–32. muscle seldom recognized on MR imaging. AJR Am J Roentgenol 166: Diogo R, Molnar J 2014 Comparative anatomy, evolution, and homologies 1057–60. of tetrapod hindlimb muscles, comparison with forelimb muscles, and Reider B, Marshall JL, Koslin B et al 1981 The anterior aspect of the knee deconstruction of the forelimb­hindlimb serial homology hypothesis. joint. J Bone Joint Surg Am 63:351–6. Anat Rec 297:1047–75. Roth C, Jacobson J, Jamadar D et al 2004 Quadriceps fat pad signal intensity Evans HE 2013 Miller’s Anatomy of the Dog, 4th ed. St Louis: Elsevier, and enlargement on MRI: prevalence and associated findings. AJR Am pp. 262–63. J Roentgenol 182:1383–7. Getty R 1975 Sisson and Grossman’s The Anatomy of the Domestic Animals, Sakuma E, Sasaki Y, Yamada N et al 2014 Morphological characteristics of
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5th ed. Philadelphia: WB Saunders Company. Volume 1 p. 852, Vol 2 the deep layer of articularis genus muscle. Folia Morphol 73:309–13. p. 1531. Toscano AE, Moraes ASR, Almeida SKS 2004 The articular muscle of the Glenn LL, Samojla BG 2002 A critical reexamination of the morphology, knee: morphology and disposition. Int J Morphol 22:303–6. neurovasculature, and fiber architecture of knee extensor muscles in Tubbs RS, Oakes WJ, Salter EG 2006 The subanconeus muscle. Folia Morphol animal models and humans. Biol Res Nurs 4:128–41 (Warsz) 65:22–5. Hepburn D 1892 The comparative anatomy of the muscles and nerves of Woodley SJ, Latimer CP, Meikle GR et al 2012 Articularis genus: an anatomic the superior and inferior extremities of the anthropoid apes. Myology and MRI study in cadavers. J Bone Joint Surg Am 94:59–67. of the inferior extremity. J Anat Physiol 26:324–56. Kimura K, Takahashi Y 1987 M. articularis genus. Observations on arrange­ ment and consideration of function. Surg Radiol Anat 9:231–9.
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