Meckel’s diverticulum complicated by acute intestinal obstruction : a case report

A. Niasse, Abdoulaye Ndiaye, Papa Souleymane Dieng, Mactar Dieng, A. Ndong, Mamadou Cissé, M. Dieng, Ibrahima Konaté
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Abstract

Meckel’s diverticulum is a rare congenital intestinal anomaly that can cause sometimes serious complications. Our aim is to review the literature on this condition by reporting the clinical case of a young adult with Meckel’s diverticulum complicated by acute intestinal obstruction. this was a 24-year-old young man, operated on for open bladder stones, received for occlusive syndrome. Abdominal CT suggested a flange occlusion. Surgical exploration found a Meckel’s diverticulum creating a flange around the last one. An intestinal resection was performed with direct anastomosis with simple consequences. Meckel’s diverticulum is a rare congenital intestinal anomaly. It is discovered incidentally or in the face of serious complications such as intestinal obstruction. Intestinal resection with one-stage anastomosis emerges as a standard and safe management approach. A Meckel’s diverticulum can be complicated by acute intestinal obstruction mimicking a postoperative flange that can err the diagnosis.
梅克尔憩室并发急性肠梗阻:病例报告
梅克尔憩室是一种罕见的先天性肠道畸形,有时会引起严重的并发症。我们的目的是通过报告一例患有梅克尔憩室并发急性肠梗阻的年轻成人的临床病例,回顾有关这一病症的文献。这是一名 24 岁的年轻男子,曾因开放性膀胱结石接受手术,后又因闭塞综合征接受治疗。腹部 CT 显示其腹腔内有一个凸缘闭塞。手术探查发现梅克尔憩室在最后一个憩室周围形成了一个凸缘。于是进行了肠道切除术,并直接吻合,结果很简单。 梅克尔憩室是一种罕见的先天性肠道异常。它是偶然发现的,或者在出现肠梗阻等严重并发症时才被发现。切除肠道并进行一期吻合术是一种标准而安全的治疗方法。 梅克尔憩室可并发急性肠梗阻,模仿术后的肠道瓣膜,从而误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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