婴儿膀胱外翻合并直肠外翻重复畸形 1 例：极为罕见。

Bladder exstrophy with exstrophic rectal duplication in an infant: An extremely rare case.

机构信息

Department of Pediatric Surgery, Süleyman Demirel University Medical School, Isparta, Turkey.

出版信息

Afr J Paediatr Surg. 2021 Apr-Jun;18(2):97-98. doi: 10.4103/ajps.AJPS_89_20.

DOI:10.4103/ajps.AJPS_89_20

PMID:33642407

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8232369/

Abstract

Exstrophic rectal duplication and its association with bladder exstrophy and anorectal malformation is an extremely rare clinical entity. This is a report of the second case of an exstrophic rectal duplication associated with bladder exstrophy in English literature. However, it is the first case, where all these anomalies were accompanied by an anorectal malformation.

摘要

直肠外翻性重复畸形及其与膀胱外翻和肛门直肠畸形的关联是一种极其罕见的临床实体。这是英语文献中报道的第二个伴发膀胱外翻的直肠外翻性重复畸形病例。然而，这也是首例所有这些异常均伴有肛门直肠畸形的病例。