女性新生儿直肠闭锁伴袋结肠无瘘-罕见的关联:1例报告

D. Barolia, A. Singh, H. Bathia, Vipal H Parmar, B. Mehta, S. Mehta
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引用次数: 0

摘要

背景:直肠闭锁是一种罕见的肛门直肠畸形(ARM)。袋结肠是一种由瘘管连接的结肠远端异常扩张。无瘘袋结肠极为罕见。病例介绍:我们报告一例不寻常的关联直肠闭锁与袋结肠无瘘的女性新生儿。在手术中,发现IV型袋结肠,切除结肠造口术作为初始手术。结论:女童直肠闭锁合并先天性袋结肠无泌尿生殖系统瘘是一种极为罕见的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rectal atresia with pouch colon without fistula in a female newborn– a rare association: A case report
Background: Rectal atresia is a rare variant of anorectal malformation (ARM). Pouch colon is an abnormal dilation of the colon distally connected by the fistula. Pouch colon without fistula is extremely rare. Case Presentation: We report a case of unusual association of rectal atresia with pouch colon without fistula in a female newborn. At surgery, a type IV pouch colon was found which was resected and colostomy was done as the initial procedure. Conclusion: Rectal atresia with congenital pouch colon without genitourinary fistula in a female child is an extremely rare association.
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