Baverman Julie, Fleischman Mariah, Brooks David
Department of Pediatrics, Creighton University School of Medicine, Omaha, Nebraska, USA.
Case Rep Pediatr. 2025 Apr 28;2025:9504629. doi: 10.1155/crpe/9504629. eCollection 2025.
A male neonate was born at 40 weeks and 3 days gestation with bilateral, stellate shaped truncal lesions, consistent with type V aplasia cutis congenita (ACC). The infant was the survivor of a dichorionic diamniotic twin pregnancy, with fetal demise documented at 13 weeks gestation. Here we present a unique case of ACC associated with fetal papyraceus, along with a review of the current literature on this heterogeneous group of disorders.
一名男性新生儿在妊娠40周零3天时出生,患有双侧星状躯干病变,符合V型先天性皮肤发育不全(ACC)。该婴儿是双绒毛膜双羊膜囊双胎妊娠的幸存者,妊娠13周时有一胎胎儿死亡记录。在此,我们报告一例与压扁胎相关的ACC罕见病例,并对有关这一异质性疾病组的现有文献进行综述。