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五型先天性皮肤发育不全合并纸样胎儿见于双绒毛膜双羊膜囊双胎妊娠

Aplasia Cutis Congenita Type V Associated With Fetus Papyraceus in a Dichorionic Diamniotic Twin Pregnancy.

作者信息

Baverman Julie, Fleischman Mariah, Brooks David

机构信息

Department of Pediatrics, Creighton University School of Medicine, Omaha, Nebraska, USA.

出版信息

Case Rep Pediatr. 2025 Apr 28;2025:9504629. doi: 10.1155/crpe/9504629. eCollection 2025.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1406/12052441/c8e0080c37bb/CRIPE2025-9504629.001.jpg

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