Portnoy Y, Metzker A
Helv Paediatr Acta. 1981 Jul;36(3):281-5.
Two cases of aplasia cutis congenita (ACC) are reported. They are unusual in that they presented in the lower extremities, showed blistering and were familial in nature. These lesions tend to heal without surgical intervention and with minimal scarring, and thus the patient can usually be assured of a happy outcome. All these characteristics support the belief that we deal either with a special entity within ACC or an entirely different syndrome.
报告了两例先天性皮肤发育不全（ACC）病例。它们的不同寻常之处在于病变出现在下肢，表现为水疱，且具有家族性。这些病变往往无需手术干预即可愈合，瘢痕形成极少，因此通常可确保患者获得良好预后。所有这些特征支持这样一种观点，即我们所处理的要么是ACC中的一种特殊类型，要么是一种完全不同的综合征。
