Achiron R, Hamiel-Pinchas O, Engelberg S, Barkai G, Reichman B, Mashiach S
Department of Obstetrics and Gynecology, Chaim Sheba Medical Center, Tel Hashomer, Israel.
Prenat Diagn. 1992 Sep;12(9):765-71. doi: 10.1002/pd.1970120909.
Aplasia cutis congenita associated with epidermolysis bullosa and pyloric atresia is a rare congenital disease in which localized or widespread areas of skin are absent at birth. Alphafetoprotein (AFP) and skin biopsy have been used for prenatal diagnosis of this condition. A patient in whom normal levels of amniotic AFP at 16 weeks' gestation presumably excluded the disease and who was at risk for aplasia cutis congenita associated with epidermolysis bullosa and pyloric atresia is described. However, 10 weeks later, ultrasonographic examination revealed hydramnios, a dilated stomach, a deformed external ear, and a contracted fisted hand. All signs were confirmed postnatally. The role of ultrasonography and the value of other diagnostic methods in this congenital disease are discussed.
先天性皮肤发育不全合并大疱性表皮松解症和幽门闭锁是一种罕见的先天性疾病,出生时局部或广泛皮肤区域缺失。甲胎蛋白(AFP)和皮肤活检已用于该疾病的产前诊断。本文描述了一名患者,其妊娠16周时羊水中AFP水平正常,推测可排除该病,但该患者有先天性皮肤发育不全合并大疱性表皮松解症和幽门闭锁的风险。然而,10周后,超声检查显示羊水过多、胃扩张、外耳道畸形和握拳状手。所有体征在出生后均得到证实。文中讨论了超声检查在这种先天性疾病中的作用以及其他诊断方法的价值。