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先天性袋状结肠用于扩大儿童神经源性膀胱:13年随访

Use of congenital pouch colon for augmenting the neurogenic bladder in a child: a 13-year follow-up.

作者信息

Kurian Jujju Jacob, Bal Harshjeet Singh, Sen Sudipta

机构信息

Department of Paediatric Surgery, Christian Medical College, Vellore, Tamilnadu, India.

出版信息

BMJ Case Rep. 2015 Mar 12;2015:bcr2014208486. doi: 10.1136/bcr-2014-208486.

DOI:10.1136/bcr-2014-208486
PMID:25766441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4369025/
Abstract

Congenital pouch colon is an anomaly always associated with anorectal malformation, where the colon is replaced by or terminates into a large aperistaltic intestinal pouch. Vertebral anomalies leading to neurogenic bladder are rare associated malformations. The pouch is aperistaltic and thus a poor rectal substitute but this very property makes it ideal for bladder augmentation. We report the first case where the pouch has been used to augment a high-pressure neurogenic bladder.

摘要

先天性袋状结肠是一种总是与肛门直肠畸形相关的异常情况,其中结肠被一个大的无蠕动肠袋所取代或终止于该肠袋。导致神经源性膀胱的脊柱异常是罕见的相关畸形。该肠袋无蠕动,因此是一种较差的直肠替代物,但正是这一特性使其成为膀胱扩大术的理想选择。我们报告了首例使用该肠袋扩大高压神经源性膀胱的病例。

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本文引用的文献

1
Congenital pouch colon: Increasing association with low anorectal anomalies.先天性袋状结肠:与低位肛肠畸形的关联日益增加。
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Management of congenital pouch colon based on the Saxena-Mathur classification.基于萨克森纳-马图尔分类法的先天性袋状结肠的管理
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Congenital pouch colon associated with anorectal malformation: report of 2 cases.先天性袋状结肠合并肛门直肠畸形:2例报告
J Pediatr Surg. 2007 Oct;42(10):E13-6. doi: 10.1016/j.jpedsurg.2007.07.025.
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A report of 27 cases of congenital short colon with an imperforate anus: so-called 'pouch colon syndrome'.27例先天性短结肠伴肛门闭锁的报告:所谓的“袋状结肠综合征”。
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