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V型袋状结肠、梅干腹综合征和先天性前尿道皮肤瘘

Type V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula.

作者信息

Raj Prince, Birua Hirendra

机构信息

Department of Pediatric Surgery, Rajendra Institute of Medical Sciences, Ranchi.

出版信息

J Neonatal Surg. 2017 Apr 15;6(2):38. doi: 10.21699/jns.v6i2.481. eCollection 2017 Apr-Jun.

DOI:10.21699/jns.v6i2.481
PMID:28770135
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5538604/
Abstract

Congenital pouch colon (CPC) or short colon syndrome is a rare type of anorectal malformation(ARM). Type V is the rarest form of CPC. We present a 1-day-old male child with type V CPC with prune belly syndrome and congenital anterior urethrocutaneous fistula (CAUF).

摘要

先天性袋状结肠（CPC）或短结肠综合征是一种罕见的肛门直肠畸形（ARM）类型。V型是CPC最罕见的形式。我们报告一名1日龄男性患儿，患有V型CPC，合并梅干腹综合征和先天性前尿道皮肤瘘（CAUF）。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fbf/5538604/6a4143a4e091/JNS-6-38_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fbf/5538604/6a4143a4e091/JNS-6-38_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fbf/5538604/6a4143a4e091/JNS-6-38_F1.jpg

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本文引用的文献

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Congenital anterior urethrocutaneous fistula: Two case reports and review of literature.先天性前尿道皮肤瘘：两例报告并文献复习
Urol Ann. 2014 Jul;6(3):239-41. doi: 10.4103/0974-7796.134285.
2
Congenital anterior urethrocutaneous fistula associated with a stenosis of the bulbar urethra in the context of high anorectal malformation without fistula.先天性前尿道皮肤瘘合并高位无瘘型肛门直肠畸形患者的球部尿道狭窄
J Plast Reconstr Aesthet Surg. 2009 Feb;62(2):e11-3. doi: 10.1016/j.bjps.2008.04.050. Epub 2008 Aug 9.