Bitemporal Aplasia Cutis Congenita
- 1 October 1974
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 110 (4) , 615-618
- https://doi.org/10.1001/archderm.1974.01630100071018
Abstract
Aplasia cutis congenita is an uncommon entity and is very rarely found on the face. A girl had an unusual bilateral, symmetrically located aplasia cutis congenita of the temples, with a peculiar facies and a constellation of other cutaneous findings. Aplasia cutis congenita is a rare dermatologic entity presenting in the newborn infant as localized areas of skin deficiency.1,2Most often the affected area lies in the midline and posteriorly on the scalp and measures 1 to 2 cm in diameter. The defect is most often solitary, but multiple lesions may occur, which are usually symmetrically located. Aplasia cutis presents at birth as sharply marginated, raw, granulating wounds and may range in shape from circular to elongate, stellate, and triangular.3These defects may reach enormous sizes, sometimes covering most of the scalp, and they are apt to be large when located on the trunk or limbs.4TheKeywords
This publication has 6 references indexed in Scilit:
- Congenital Skin DefectsDermatology, 1967
- CONGENITAL ABSENCE OF SKINPlastic and Reconstructive Surgery, 1960
- CONGENITAL DEFECT OF THE SCALPPlastic and Reconstructive Surgery, 1948
- Congenital Skin Defect of the NewbornArchives of Disease in Childhood, 1948
- CONGENITAL DEFECT OF THE SKIN OF THE NEW-BORNArchives of Dermatology, 1935
- CONGENITAL SKIN DEFECTSArchives of Pediatrics & Adolescent Medicine, 1917