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Syn Dactyl y
Syn Dactyl y
Patients are placed supine with the affected upper limb supported on a
hand table. A nonsterile tourniquet is placed in the upper brachium,
taking care to maintain access to the antecubital fossa, if full-
thickness skin graft is to be taken from that site.
If skin graft from the inguinal crease is to be harvested, the ipsilateral
groin is also prepped and draped sterilely into the surgical field.
Skin graft from the inguinal region should be
taken well lateral to the palpated femoral pulse to
minimize harvest of hair-bearing skin, and a
surgical marking pen may be placed into the
inguinal crease with the hip flexed to identify the
most aesthetic axis from which to harvest skin;
this will allow for easy primary closure of the
harvest site with a scar that lies inconspicuously
in the skin folds.
GRAFTLESS SYNDACTYLY RELEASE
Vascularized skin from the dorsum
of the hand is raised and advanced
to reconstitute the web commissure,
leaving the skin over the dorsal
aspects of the adjacent proximal
phalanges available to cover the
separated digits.
The resulting donor defect is closed
primarily in the fashion of a V-Y
advancement fl ap. Areas of skin
eficiencies distal to the web
commissure are closed primarily
with interdigitating skin flaps after
aggressive defatting.
FIRST WEB SYNDACTYLY
It is imperative that a wide, deep
first web space is reconstituted to
optimize hand function, and
reconstructed using a single,
scarless, vascularized flap of
native tissue.
Ghani modification of the Buck-
Gramcko flap is currently used
and patients are positioned as
previously described. The
planned skin incisions are
marked on the dorsum of the
hand,
Dorsally, the distal transverse extent of the flap
lies at the junction of the distal one-third and
proximal two-thirds of the thumb proximal
phalanx. The radial incision lies over the thumb
metacarpal. The ulnar incision is curvilinear—
almost bilobed—extending from the index to the
small metacarpal
APERT AND COMPLEX POLYSYNDACTYLY
Apert syndrome, or acrocephalosyndactyly, refers to a constellation of
clinical manifestations including coronal craniosynostosis, midface
hypoplasia, and characteristic syndactylies of the hands and feet,
due to a mutation in the FGFR2 gene on chromosome 10q. Hand
involvement classified by Upton as well as Van Heest.
TYPE OF APERT AND COMPLEX
POLYSYNDACTYLY
Type I hands (spade hand) have incomplete first web
syndactylies with a relative flat central mass and good
MCP joints with varying degrees of symphalangism and
IP stiffness.
Type II hands (mitten or spoon hand) have complete
syndactylies of the first and fourth webs with fusion of
the digital tips and increasing concavity of the palm.
Type III hands (hoof or rosebud hands) represent
complete complex syndactylies of all digits in which the
thumb is incorporated into the central, cupped hand
mass with a single synonychia.
POSTOPERATIVE
Patients remain in casts for 3 to 4 weeks, after which casts are
removed and wounds examined.
While not necessary, our preference is to have patients work with
our occupational therapists for scar mold (silicone or elastomere),
scar massage, and range-of-motion exercises to optimize healing.
COMPLICATION
Digital necrosis is the most serious
potential complication, though it is
rare if the surgical principles are
followed.
Skin graft failure may result from
hematoma formation beneath
and/or shear stresses imparted upon
the grafts in the postoperative
period. This risk may be greater in
younger patients, in whom
appropriate graft tensioning is more
difficult and in whom postoperative
immobilization is a greater
challenge.
Nail plate deformity is common after complete
syndactyly release in the presence of a synonychia.
“Web creep” refers to the distal migration of the
reconstructed interdigital commissure with continued
growth and is a common occurrence following
syndactyly release. Some evidence suggest that the
risk of web creep may be diminished if release is
performed after 18 months of age.
Hypertrophic scar and true keloid formation may
lead to unsightly and dysfunctional digits following
syndactyly release