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先天性袋状结肠:产前诊断与视频辅助管理

Congenital pouch colon: antenatal diagnosis and video-assisted management.

作者信息

Lopater Jonathan, Hery Géraldine, Haddad Mirna, Ughetto Fabrice, Gorincour Guillaume, Fernandez Carla, Guys Jean Michel, de Lagausie Pascal

机构信息

Pediatric Surgery Department, La Timone Children Hospital, 264, rue Saint Pierre, Marseille Cedex 05, France.

出版信息

Pediatr Surg Int. 2010 Jul;26(7):759-61. doi: 10.1007/s00383-010-2589-2. Epub 2010 Mar 23.

DOI:10.1007/s00383-010-2589-2
PMID:20309564
Abstract

Congenital pouch colon (CPC) is an unusual abnormality associating a pouch-like dilatation of a shortened colon with an anorectal malformation (ARM). There are few reports of CPC in Europe, a contrario it represents up to 15% of ARM in India. Coloplasty and excision are described in the surgical management. This report describes a new case of CPC. This is the first reported case with a prenatal clinical presentation as an hypoechogenic abdominal image at ultrasound and a video-assisted management.

摘要

先天性袋状结肠(CPC)是一种罕见的异常情况,表现为缩短的结肠呈袋状扩张并伴有肛门直肠畸形(ARM)。欧洲关于CPC的报道较少,相反,在印度它占ARM的比例高达15%。手术治疗方法包括结肠成形术和切除术。本报告描述了一例CPC新病例。这是首例产前经超声检查表现为腹部低回声图像且采用视频辅助治疗的病例报告。

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本文引用的文献

1
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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Bladder outlet obstruction causes fetal enterolithiasis in anorectal malformation with rectourinary fistula.膀胱出口梗阻在伴有直肠泌尿瘘的肛门直肠畸形中导致胎儿肠结石症。
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直肠肛门畸形治疗标准制定国际会议初步报告
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Laparoscopically assisted anorectal pull-through for high imperforate anus--a new technique.腹腔镜辅助下高位肛门闭锁的直肠拖出术——一种新技术
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