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先天性囊状结肠伴直肠闭锁:一例报告。

Congenital pouch colon with rectal atresia: a case report.

机构信息

Department of Paediatric Surgery, K.E.M. Hospital and Seth G.S. Medical College, Mumbai, India.

出版信息

J Pediatr Surg. 2010 Mar;45(3):639-41. doi: 10.1016/j.jpedsurg.2009.12.028.

Abstract

The association of congenital pouch colon with rectal atresia is quite rare with only 2 cases previously reported in literature. We describe the third such case and the second instance to survive. Although the prior survivor was managed by a single-stage procedure, we successfully managed our case by staged procedures. In this case report, we discuss the etiology and surgical options available for this rare condition.

摘要

先天性囊状结肠与直肠闭锁的关联非常罕见,文献中仅有 2 例先前报道。我们描述了第 3 例也是第 2 例存活的病例。尽管先前的幸存者通过单阶段手术进行了治疗,但我们通过分阶段手术成功地治疗了我们的病例。在本病例报告中,我们讨论了这种罕见情况的病因和可用的手术选择。

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引用本文的文献

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Congenital pouch colon: Case report and literature review.
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Congenital Pouch Colon with Rectal Atresia Revisited.
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Congenital Pouch Colon with Rectal Atresia: A Rare Association.
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