Abstract: | Aplasia cutis congenita (ACC) is an uncommon congenital disease characterized by focal absence of the epidermis, subcutaneous tissue, galea, and, in rare cases, calvarial bone. We herein show that a boy born with ACC presented with a large scalp and skull defect and was treated conservatively with wet dressings. This conservative approach produced complete epithelialization of the skin defect with secondary closure of the cranial vault. |