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Congenital Thumb
Deformities
Dr Mujtuba Pervez Khan
Resident Plastic Surgery
DUHS/CHK
• Apical Ectodermal Ridge = Growth in proximal to distal direction
• Zone of Polarizing Activity = Antero-posterior growth
• Non ridge ectoderm = Dorso-ventral growth
Thumb Hypoplasia
• Normal thumb is just proximal to the PIPJ of the index finger
• Isolated
• Part of radial deficiency with normal forearm
workup
• CBC
• echo
• X-ray spine
• U/S KUB
• X-ray Radius/Ulna
• X-ray tibia/fibula
• Chromosome challenge test
Type 1 Hypoplasia
• Generalized hypoplasia usually involves thenar muscles
• functional deficit -> tendon transfer
Type 2 hypoplasia
• Absence of muscles innervated by recurrent branch median nerve (APB,
OPB, superficial head of FPB)
• Deep head of FPB provides MCPJ flexion
• MCPJ flexion is unstable due to UCL insufficiency, Both UCL and RCL may
be involved
• Narrow 1st web space, appears less narrow due to valgus position of MCPJ
Type 2 hypoplasia
• 1st web space narrowing -> z-plasty,
• extremely tight web may require partial release of Adductor/1st dorsal
interosseous
• UCL or/and RCL reconstruction by tendon graft
• Chondrodesis for stable MCPJ
• Release of pollex abductus for pollex abductus
• Tendon transfer for opposition
• FDS middle/ring finger, EIP, ECU, Adm
Type 3 hypoplasia
• Type 2 + absence or hypoplasia of EPL, EPB, FPL
• Stable CMC (3A) -> reconstruction
• Trapezio-metacarpal joint ossify at 6 years. X-rays before this age will be
unreliable
• MRI
• Wide index and long finger web space
Unstable CMC (3B), Type 4, Type 5 -> Policization
Clasped Thumb
• Type 1 : Extensor mechanism absent/hypoplastic
• Type 2 : Type 1 + Joint contracture, Collateral ligament abnormality, 1st web
space contracture, Thenar muscle abnormality
• Type 3 : Mild or no extensor abnormality, Arthrogryposis, associated
syndromes MASA (mental retardation, aphasia, shuffling gait,
adducted thumb)
C/F :
• Thumb in flexion
• Extension lag at MCPJ, may also be present at IPJ
• EPB most commonly involved
• +/- APL, EPL
Treatment
• No treatment for mild MCPJ extension lag
• Splintage 2-6 months
• Surgery for failed splinting or if present after 2 years
• 1st web space contracture -> z plasty (4 flap plasty) / dorsal rotation
advancement flap
• Tendon transfer (EIP, EDM, FDS) for extensors
• Thumb spika for 6 weeks, night splintage for the next 6 weeks
Triphalangeal Thumb
• Autosomal dominant, can also be sporadic
• May be isolated or associated with
1. Holt Oram Syndrome
2. Fanconi’s anemia
3. Wassel type VII thumb duplication
4. Thumb hypoplasia
5. Polydactyly
6. Syndactyly
7. Central deficiency
Type 1: Relatively normal appearing thumb with an extra phalanx of
variable size
Triangular, trapezoidal, rectangular shaped
Type 2: Fully developed phalanx
Management Between 12-18 months – oppositional pinch
Length and angulation
• extra bone may show no growth and require no treatment
• excess growth and angulation in ulnar direction -> Surgery
• extra phalanx excision and collateral ligament reconstruction
• Joint stiffness, instability, insufficient motion are common problems
Extra interphalangeal joint
• excision of phalanx should not be done due to instability
• Fusion of abnormal phalanx with distal OR proximal phalanx, bone
shortening
• Joint with the greatest motion is preserved
Management
Thumb index web space
• z plasty / rotational advancement flap
• Type 2 has no web space -> policization
Opposition
• Tendon transfer (FDS, ADM)
Thanks.

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Congenital Thumb Deformities

  • 1. Congenital Thumb Deformities Dr Mujtuba Pervez Khan Resident Plastic Surgery DUHS/CHK
  • 2. • Apical Ectodermal Ridge = Growth in proximal to distal direction • Zone of Polarizing Activity = Antero-posterior growth • Non ridge ectoderm = Dorso-ventral growth
  • 3.
  • 5. • Normal thumb is just proximal to the PIPJ of the index finger • Isolated • Part of radial deficiency with normal forearm
  • 6.
  • 7. workup • CBC • echo • X-ray spine • U/S KUB • X-ray Radius/Ulna • X-ray tibia/fibula • Chromosome challenge test
  • 8.
  • 9. Type 1 Hypoplasia • Generalized hypoplasia usually involves thenar muscles • functional deficit -> tendon transfer Type 2 hypoplasia • Absence of muscles innervated by recurrent branch median nerve (APB, OPB, superficial head of FPB) • Deep head of FPB provides MCPJ flexion • MCPJ flexion is unstable due to UCL insufficiency, Both UCL and RCL may be involved • Narrow 1st web space, appears less narrow due to valgus position of MCPJ
  • 10. Type 2 hypoplasia • 1st web space narrowing -> z-plasty, • extremely tight web may require partial release of Adductor/1st dorsal interosseous • UCL or/and RCL reconstruction by tendon graft • Chondrodesis for stable MCPJ • Release of pollex abductus for pollex abductus • Tendon transfer for opposition • FDS middle/ring finger, EIP, ECU, Adm
  • 11. Type 3 hypoplasia • Type 2 + absence or hypoplasia of EPL, EPB, FPL • Stable CMC (3A) -> reconstruction • Trapezio-metacarpal joint ossify at 6 years. X-rays before this age will be unreliable • MRI • Wide index and long finger web space Unstable CMC (3B), Type 4, Type 5 -> Policization
  • 12.
  • 13.
  • 14.
  • 16. • Type 1 : Extensor mechanism absent/hypoplastic • Type 2 : Type 1 + Joint contracture, Collateral ligament abnormality, 1st web space contracture, Thenar muscle abnormality • Type 3 : Mild or no extensor abnormality, Arthrogryposis, associated syndromes MASA (mental retardation, aphasia, shuffling gait, adducted thumb)
  • 17. C/F : • Thumb in flexion • Extension lag at MCPJ, may also be present at IPJ • EPB most commonly involved • +/- APL, EPL
  • 18. Treatment • No treatment for mild MCPJ extension lag • Splintage 2-6 months • Surgery for failed splinting or if present after 2 years • 1st web space contracture -> z plasty (4 flap plasty) / dorsal rotation advancement flap • Tendon transfer (EIP, EDM, FDS) for extensors • Thumb spika for 6 weeks, night splintage for the next 6 weeks
  • 20. • Autosomal dominant, can also be sporadic • May be isolated or associated with 1. Holt Oram Syndrome 2. Fanconi’s anemia 3. Wassel type VII thumb duplication 4. Thumb hypoplasia 5. Polydactyly 6. Syndactyly 7. Central deficiency
  • 21. Type 1: Relatively normal appearing thumb with an extra phalanx of variable size Triangular, trapezoidal, rectangular shaped Type 2: Fully developed phalanx
  • 22. Management Between 12-18 months – oppositional pinch Length and angulation • extra bone may show no growth and require no treatment • excess growth and angulation in ulnar direction -> Surgery • extra phalanx excision and collateral ligament reconstruction • Joint stiffness, instability, insufficient motion are common problems Extra interphalangeal joint • excision of phalanx should not be done due to instability • Fusion of abnormal phalanx with distal OR proximal phalanx, bone shortening • Joint with the greatest motion is preserved
  • 23. Management Thumb index web space • z plasty / rotational advancement flap • Type 2 has no web space -> policization Opposition • Tendon transfer (FDS, ADM)