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一例罕见的苹果皮样回肠闭锁合并结肠闭锁病例:手术治疗及结果

A Rare Case of Apple Peel Ileal Atresia With Coexisting Colonic Atresia: Surgical Management and Outcomes.

作者信息

Sadecka Aleksandra I, Jasinska Aleksandra

机构信息

Department of Pediatric Surgery, Medical University of Warsaw, Warsaw, POL.

出版信息

Cureus. 2025 Jun 18;17(6):e86290. doi: 10.7759/cureus.86290. eCollection 2025 Jun.

Abstract

Ileal atresia is one of the most frequent causes of congenital intestinal obstruction. Type IIIb, also known as apple peel atresia, is the least common subtype. Colonic atresia is a rare anomaly that can also cause neonatal intestinal obstruction. Both can coexist with other atypical malformations, further complicating diagnosis. The surgical management of these two gastrointestinal malformations differs between centers, and no standardized procedural guidelines currently exist. We present a case of a neonate born with apple peel ileal atresia coexisting with transverse colonic atresia, both successfully treated with primary anastomoses. The postoperative course was uneventful, and the patient was discharged with full oral feeding and regular bowel movements.

摘要

回肠闭锁是先天性肠梗阻最常见的病因之一。IIIb型,也称为苹果皮样闭锁,是最不常见的亚型。结肠闭锁是一种罕见的畸形,也可导致新生儿肠梗阻。两者都可能与其他非典型畸形并存,使诊断更加复杂。这两种胃肠道畸形的手术治疗在不同中心存在差异,目前尚无标准化的手术指南。我们报告一例新生儿,患有苹果皮样回肠闭锁并伴有横结肠闭锁,两者均通过一期吻合成功治疗。术后过程顺利,患者出院时能完全经口喂养且排便正常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d88/12175975/0ed2b5e84c09/cureus-0017-00000086290-i01.jpg

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