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Colostomy prolapse and hernia following window colostomy in congenital pouch colon

机译:先天性袋结肠结肠造口术后结肠造口脱出和疝气

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摘要

Congenital pouch colon, a variant of anorectal malformation, is a rare anomaly with a high incidence in North India and although the anatomy and diagnostic features have been well described, the surgical treatment continues to be challenging. This report describes the complications following a less preferred but often practised surgical option—a temporizing window colostomy in three babies. A window colostomy predisposes to prolapse of the entire pouch colon with herniation of bowel loops, intestinal obstruction and failure to thrive. Depending on the state of the child, either a proximal diverting stoma or tubularization of the pouch with a terminal stoma is recommended as the procedure of choice for the initial surgical management of this complex and rare malformation.
机译:先天性袋结肠是肛门直肠畸形的一种变体,在印度北部是一种罕见的异常现象,发病率很高,尽管其解剖学和诊断特征已经得到了很好的描述,但是外科手术治疗仍然具有挑战性。该报告描述了不太受欢迎但经常采用的外科手术后的并发症-在三个婴儿中进行临时窗结肠造口术。开窗结肠造口术容易使整个小肠结肠脱出,并伴有肠loop突出,肠梗阻和failure壮成长。根据孩子的状态,建议对这种复杂且罕见的畸形进行初始手术治疗时,选择近端转移造口或袋装管状导管并带有最终造口。

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