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Home / Foot and Ankle / Pes cavus - deformity and causes
Foot and Ankle

Pes cavus - deformity and causes

Cavus arch patterns with neurological causes such as Charcot-Marie-Tooth and Friedreich ataxia

45 questions 4 source pages 3 images

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45 questions
Q1Describe the clinical photo of an adult acquired flatfoot.📷▸
Describe photo:
Describe photo:
  • Adult with forefoot abduction
  • Decreased medial foot arch (midfoot supinated in relation to hindfoot)
  • Hindfoot valgus
  • Medial prominence
Q2What is the differential diagnosis of acquired flatfoot (bilateral vs unilateral)?▸
  • Bilateral/any: PTTD, tarsal coalition, congenital vertical talus
  • Unilateral: post-traumatic (Lisfranc, spring ligament injury), degenerative, Charcot
  • Bilateral systemic: rheumatoid arthritis, neuromuscular (spina bifida), cerebral palsy
  • Generalised ligamentous laxity (Marfan, Ehlers-Danlos)
Q3What are the possible sources of pain in acquired flatfoot?▸
  • Medial: PTT, deltoid ligament, tarsal tunnel
  • Lateral: subfibular impingement
  • Heel: plantar aponeurosis, retrocalcaneal bursitis
  • Diffuse: ankle, subtalar joint
  • Proximal: knee, back; distal: bunion, metatarsal heads
Q4How do you clinically assess a flatfoot?▸
  • Determine whether the flatfoot and hindfoot valgus are flexible or rigid, and identify cause and complications (arthritis)
  • Inspection: double heel raise and single leg heel raise (PT power, flexibility)
  • Too many toes sign, navicular bulging signifying accessory navicular; look for scars (post trauma)
  • Palpate sinus tarsi, deltoid ligament, PTT; test PT, FDL/ FHL power (transfer)
  • Subtalar ROM and residual forefoot supination with correction; Silverskiold test
  • Beighton score, check hands for RA, check spine if bilateral; assess gait
  • X-ray: weight-bearing DP (Simmons angle, talocalcaneal angle, talus uncoverage) and lateral (Meary angle, calcaneal pitch, foot collapse at TN/NC/TTJ), No feature of previous fracture/ fragmentation, Saltzman view for hindfoot alignment, XR ankle mortise, Scannogram for LL alignment, MRI for PTT
  • Bloods to rule out RA
Q5How is the foot arch maintained and what is the pathophysiology of PTTD?▸
  • Medial longitudinal arch static support: bony (calcaneum, talus, navicular, medial 3 rays) and soft tissue (spring ligament, plantar aponeurosis, deltoid ligament)
  • Dynamic support: PTT, peroneus longus and intrinsics
  • Lateral arch: calcaneum, cuboid, lateral 2 rays with long and short plantar ligaments, bifurcate ligament
  • Transverse arch: keystone is 2nd MT and middle cuneiform, supported by the Lisfranc ligament
  • Pathophysiology: PTT tenosynovitis causes loss of dynamic support, failure to lock the transverse tarsal joint --> further cause static stabilizer to fail
  • Result: loss of one foot of the tripod, hindfoot valgus, MF/FF compensatory supination to maintain the tripod; PTT has a watershed blood supply 2-6cm proximal to insertion
Q6What is the aim of management in adult acquired flatfoot?▸
  • Stable, plantigrade, painless foot
  • Rebalance the foot through bone and/or soft tissue to restore a balanced tripod
  • Treat according to the patient's symptoms
Q7What is the anatomy and action of the posterior tibialis tendon (PTT)?▸
  • Origin: posterior fibula, tibia and interosseous membrane
  • Inserts: navicular tuberosity, 1st – 3rd cuneiform, cuboid, 2-4 metatarsals, sustentaculum tali
  • Invertor of the subtalar joint
  • Plantarflexion of the ankle joint
  • Adductor of the forefoot
  • Watershed blood supply 2-6cm proximal to insertion
Q8What is the Johnson classification of PTTD?▸
  • 1: PTT power intact, no flatfoot
  • 2: A flexible flatfoot, B abducted forefoot, C forefoot varus
  • 3: Subtalar joint arthritis
  • 4: Deltoid ligament insufficiency
Q9How is stage 1 PTTD managed?▸
  • Physio for TA stretching
  • Orthosis: UCBL, moulded AFO, medial heel wedge, longitudinal arch support
  • Tenosynovectomy
Q10How is stage 2 PTTD managed?▸
  • Combination of bony + soft tissue procedure, tailored to the individual’s deformities and muscle imbalance
  • Soft tissue: FHL or FDL tendon transfer; TA lengthening also protects the transfer; +/- spring ligament reconstruction
  • Coronal plane bone: calcaneal wedge osteotomy (85% pain relief/improved function at mean 15y, Chadwick BJJ 2015)
  • Sagittal plane bone: 1st TMTJ fusion or Cotton medial cuneiform opening wedge osteotomy for forefoot varus - restores tripod
  • Transverse plane bone: lateral column lengthening for forefoot abduction - protect FDL transfer
Q11Which tendon transfer is preferred for PTTD - FHL or FDL?▸
  • FHL is stronger
  • FDL gives better functional outcomes because FHL is harder to mobilise
Q12How are stage 3 and stage 4 PTTD managed?▸
  • Stage 3: subtalar fusion +/- triple or double (TN + subtalar) fusion
  • Double fusion (TN + subtalar) has similar functional scores and shorter OT time (Int Orthop 2021 Fadle)
  • Stage 4: deltoid ligament reconstruction +/- ankle replacement or fusion
Q13What is the FAI 2020 consensus statement on adult acquired flatfoot?▸
  • Rename the condition Progressive Collapsing Foot Deformity (PCFD)
  • New classification to stage the deformity
  • A: hindfoot valgus deformity
  • B: midfoot/forefoot abduction deformity
  • C: forefoot varus/medial column instability
  • D: peritalar subluxation/dislocation
  • E: ankle instability
Q14What is the role of arthroereisis in flatfoot?▸
  • Subtalar arthroereisis induces a triplanar modification of the foot limiting pronation
  • EFFORT review 2017 and AAOS 2021: no long-term studies, only poor quality evidence supporting its use
Q15What are the positions of fusion in a triple arthrodesis?▸
  • Subtalar joint 5 degrees valgus (TA is not a deforming force)
  • TN joint: adequate coverage of the talar head; restore hindfoot-forefoot relationship so the 1st and 5th MT heads both touch the ground
  • Restore the height of the medial arch
  • CC joint: neutral (in situ)
Q16Describe the clinical features of a cavovarus foot.📷▸
High medial arch, hindfoot varus, midfoot cavus, forefoot adducted and pronated
High medial arch, hindfoot varus, midfoot cavus, forefoot adducted and pronated
  • High medial arch with midfoot cavus
  • Hindfoot varus, forefoot adducted and pronated in relation to hindfoot
  • Claw toes, peek-a-boo heel sign
Q17What do you ask about in the history of a cavovarus foot?▸
  • History of neurological disease, family history (CMT)
  • Instability, metatarsalgia, fatigue, shoewear problems
  • Callus, ulcers, pain (OA), stress fractures, Muller Weiss
  • Functional limitation and expectations
Q18What are the examination findings in cavovarus foot?▸
  • LL muscle wasting - inverted champagne bottle appearance
  • Forefoot clawing, adduction, pronation; midfoot cavus; hindfoot varus equinus
  • Coleman block test for flexibility and forefoot-driven deformity
  • Gait: broad based ataxic gait; check lateral ankle instability (ATFL, CFL)
  • Full neuro exam (cerebellar), sensation, spine and hands
Q19Explain the Coleman block test.▸
  • Decides whether cavovarus is hindfoot or forefoot driven and whether flexible
  • Block supports the 5th MT and heel, freeing the 1st MT
  • Hindfoot corrects if the deformity is forefoot driven and flexible
  • Rationale: hindfoot varus is compensatory to keep the lateral rays on the ground
Q20How is cavovarus foot managed surgically?▸
  • Combination of bony procedure with soft tissue procedure, tailored to the individual’s deformities and muscle imbalance
  • Flexible: bony + soft tissue procedures for forefoot and midfoot +/- TA lengthening
  • Rigid: add midtarsal and hindfoot bony procedures
  • Arthritis/progressive disease: fusion
  • Soft tissue: PL to PB transfer, Steindler plantar aponeurosis release
  • Bone: Dwyer lateral closing wedge calcaneal osteotomy, 1st ray dorsiflexion osteotomy, triple arthrodesis
Q21What additional examination findings are checked in cavovarus foot?▸
  • Sole: callosities and ulcers
  • Scars and correctability
  • Muscle power: PT, PB, tib ant, PL
  • Lateral ankle instability (ATFL and CFL)
  • Silverskiold test
Q22What is a cavus foot?▸
  • Fixed plantar flexion deformity of the forefoot in relation to the hindfoot
  • Results in an abnormally high arch
  • 2/3 are neurological
Q23What are the causes of cavus foot?▸
  • Neurological: CP/stroke/Friedreich's ataxia
  • Neurological: syringomyelia/diastematomyelia/spina bifida
  • Neurological: SMA, polio, CMT, DMD
  • Non-neurological: post-traumatic (Volkmann contracture, talar neck malunion)
  • Non-neurological: residual club foot
Q24What are the X-ray findings in cavovarus foot?▸
  • DP: talocalcaneal angle and talo-1st MT angle
  • Lateral: see-through sign, calcaneal pitch, Meary angle, calcaneal-1st MT angle (Hibb's angle N>150)
  • Lateral: lateral kite angle <25 (parallelism), double talar head sign, bell-shaped cuboid
  • Look for degeneration; obtain ankle mortise and Saltzman view
  • MRI spine if neurological disease is suspected
Q25When is a neurologist referral made in cavovarus foot and what tests are requested?▸
  • Refer if neurological disease is suspected
  • ECG NCS
  • Sural nerve biopsy, muscle biopsy, CK
Q26What is the aim and conservative management of cavovarus foot?▸
  • Systemically delineate and treat the underlying cause
  • Locally provide a plantigrade, stable, pain-free, shoeable, preferably mobile foot
  • Conservative: physio for stretching and accommodative shoewear to relieve pressure
Q27How is surgical management of cavovarus foot tailored to flexibility?▸
  • Flexible: bony + soft tissue procedure for forefoot and midfoot; hindfoot should correct with these +/- TA lengthening
  • Rigid: add midtarsal + hindfoot bony procedure
  • Arthritis/progressive disease: fusion
  • +/- lateral ankle ligamentous reconstruction if ankle instability
Q28What soft tissue procedures are used in cavovarus foot?▸
  • Hindfoot varus: PL to PB transfer
  • Hindfoot varus: PT to cuneiform transfer
  • Hindfoot varus: tib ant to cuneiform transfer
  • Midfoot cavus: Steindler plantar aponeurosis release
Q29What bony procedures are used in cavovarus foot?▸
  • Hindfoot: Dwyer lateral closing wedge calcaneal osteotomy
  • Hindfoot: lateral calcaneal page osteotomy
  • Midfoot cavus: 1st ray dorsiflexion osteotomy
  • Midfoot cavus: TMTJ (Jahss) or tarsal (Japas) osteotomy
Q30How are claw toes in cavovarus foot managed?▸
  • PIPJ flexible: Girdlestone-Taylor FDL to EDL transfer
  • PIPJ rigid, MTPJ flexible: DuVries (P1 head + P2 base resection/fusion) + EDL tenotomy
  • PIPJ rigid, MTPJ rigid not subluxed: DuVries + EDB tenotomy + MTPJ dorsal capsulotomy + EDL lengthening
  • PIPJ rigid, MTPJ rigid and subluxed: Weil osteotomy
Q31What is the Jones procedure for the big toe in cavovarus foot?▸
  • EHL to MT neck transfer
  • Fuse the IPJ
Q32How is equinus managed in cavovarus foot surgery?▸
  • Usually corrects after the other deformities are corrected
  • TA lengthening is left until other corrections are done
Q33Explain forefoot-driven versus hindfoot-driven cavovarus.▸
  • FF driven: PL >> ATT causes 1st MT plantarflexion; PT >> PB causes hindfoot varus
  • 1st MT plantarflexion + forefoot pronation -> medial forefoot strikes ground first
  • Subtalar joint inverts to bring the lateral forefoot down, so hindfoot varus is compensatory
  • Recruited EHL causes claw toe; MTPJ extension tightens the plantar aponeurosis via the windlass, worsening cavus and varus
  • Hindfoot cavus (calcaneocavus): weak triceps surae with relatively strong PTT/FHL plantarflexing the entire forefoot
Q34What is Charcot-Marie-Tooth disease?▸
  • Hereditary motor sensory neuropathy
  • Peroneal muscle atrophy
  • Prevalence 1:2500 - most common inherited neuropathy
  • Usually autosomal dominant (can be AR or X-linked)
  • Affects motor more than sensory
Q35What is the genetic basis of CMT?▸
  • Peripheral myelin protein 22 - defective Schwann cell membrane protein
  • Causes defective myelin sheath formation
  • Duplication of chromosome 17
Q36What are the three main types of CMT?▸
  • Type 1: demyelinating, presents 10-20s, AD, cavus foot
  • Type 2: axonopathy, 20s+, flaccid foot, less disabling
  • Type 3: X-linked recessive, demyelinating + axonal degeneration
Q37What are the clinical features and diagnosis of CMT?▸
  • Equinocavovarus +/- rigid hindfoot
  • Weakened TA and peroneal muscles - foot drop during swing phase
  • Check the hands
  • Diagnosis: NCV/EMG, DNA/chromosome analysis
  • No role for nerve biopsy
Q38How is CMT managed non-operatively?▸
  • Always non op first
  • Stretching
  • Orthosis: need a solid AFO
  • No posterior leaf AFO due to inversion and eversion weakness
Q39How is CMT managed surgically?▸
  • Follow cavovarus principles
  • Traditionally fusion as the disease is progressive
  • Reconstruction has lower rates of degeneration and reoperation compared with triple arthrodesis (Ward JBJS 2008)
Q40What are the differential diagnoses of CMT?▸
  • Spina bifida
  • SMA
  • Polio
  • Friedreich ataxia
Q41What is the genetic basis of Friedreich's ataxia?📷▸
Friedreich's Ataxia
Friedreich's Ataxia
  • Autosomal recessive
  • Frataxin mutation affecting mitochondria production
Q42How is Friedreich's ataxia diagnosed?▸
  • Clinical + family history + genetic testing
  • It is the commonest spinocerebellar degenerative disease
Q43How does Friedreich's ataxia present clinically?▸
  • Staggering, wide-based gait
  • Triad: ataxia, areflexia, upgoing plantar
Q44What are the orthopaedic and systemic associations of Friedreich's ataxia?▸
  • Cavovarus foot
  • Scoliosis
  • Cardiomyopathy - assess before planning surgery
Q45What is the prognosis of Friedreich's ataxia?▸
  • Wheelchair-bound around 30 years
  • Death around 50 years