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儿童后天性结肠闭锁:三例报告并文献复习

Acquired colonic atresia in children: a report of three cases and review of the literature.

作者信息

Fouad Dina, Bethell George S, Hall Nigel J

机构信息

Department of Paediatric Surgery and Urology, Southampton Children's Hospital, Southampton SO16 6YD, United Kingdom.

University Surgery Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, United Kingdom.

出版信息

J Surg Case Rep. 2024 Aug 23;2024(8):rjae012. doi: 10.1093/jscr/rjae012. eCollection 2024 Aug.

Abstract

We describe cases of three infants who developed acquired colonic atresia presumed secondary to significant systemic cardiovascular compromise and in the absence of necrotizing enterocolitis. An acquired colonic atresia may present as feed intolerance and should be investigated with a lower gastrointestinal contrast study. We would also recommend routine lower gastrointestinal contrast study prior to stoma closure in an infant with history of significant cardiovascular compromise, even in the absence of significant widespread colonic inflammation such as necrotizing enterocolitis.

摘要

我们描述了三例婴儿病例,他们患上了后天性结肠闭锁,推测继发于严重的全身性心血管功能不全,且不存在坏死性小肠结肠炎。后天性结肠闭锁可能表现为喂养不耐受,应通过下消化道造影检查进行评估。对于有严重心血管功能不全病史的婴儿,即使不存在如坏死性小肠结肠炎等明显的广泛结肠炎症,我们也建议在造口关闭前常规进行下消化道造影检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b93c/11342861/42f7efb88b6d/rjae012f1.jpg

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