先天性袋状结肠合并假性膀胱外翻：两例报告。

Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases.

作者信息

Jhanwar Praveen, Shinde Nand Kishor, Patel Jigar N, Pant Nitin, Chadha Rajiv

机构信息

Department of Pediatric Surgery, Lady Harding Medical College and Kalawati Saran Children's Hospital, New Delhi-110001.

出版信息

APSP J Case Rep. 2016 Jan 1;7(1):9. eCollection 2016 Jan-Apr.

PMID:26814054

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4715891/

Abstract

This report describes two newborn girls with single perineal opening (cloaca), and pseudoexstrophy in the form of divergent pubic bones and rectus muscles, and a low-set umbilicus. Both patients had a type II congenital pouch colon (CPC) with one hemiuterus and vagina on each side in the pelvis. In one patient, a Meckel's diverticulum was present 5 cm from the ileocecal junction. In both girls, a diverting proximal ileostomy was the initial surgery.

摘要

本报告描述了两名患有单一会阴开口（泄殖腔）的新生女婴，伴有耻骨和腹直肌分离形式的假性膀胱外翻以及低位脐。两名患者均患有II型先天性袋状结肠（CPC），盆腔两侧各有一个半子宫和阴道。其中一名患者在距回盲部交界处5厘米处存在梅克尔憩室。两名女孩最初的手术均为近端回肠转流造口术。