A child with epidermolysis bullosa and aplasia cutis congenita is presented
. This is a very rare condition that represents an unusual manifestation of
epidermolysis bullosa. Management of aplasia cutis congenita is controvers
ial and may be conservative, surgical, or a combination of the two. In this
patient, surgical treatment with split-thickness skin grafts failed, and c
onservative treatment using silver-sulfadiazine cream dressings was institu
ted.