Laparoscopic Management of Mechanical Small Bowel Obstruction Secondary to Meckel's Diverticulum with a Double Basis. A Rare Anatomic Presentation.

Pub Date : 2020-01-01 Epub Date: 2020-11-23 DOI:10.1055/s-0040-1713902
Aurora Mariani, Mohammed Siddiqui, Nicolas Boulard, Dominique Berrebi, Arnaud Bonnard
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Abstract

Meckel's diverticulum (MD) is the most common congenital abnormality of the gastrointestinal tract. Intestinal occlusion due to MD is a commonly observed consequence of intussusception or volvulus. Here, we report a case of an 11-year-old boy who presented to the emergency department with acute abdominal pain, bilious vomiting, and abdominal rebound tenderness. Computed tomography scan concluded a diagnosis of intestinal occlusion with no apparent cause. The patient was submitted to diagnostic laparoscopy, and mechanical occlusion by the permeable Meckel with double base was identified. A diverticulectomy by staplers was performed, and occlusion was alleviated. MD is a rare disease (for only 0.3-2.9% of the general population), and only 4.2 to 9% of patients diagnosed with MD have associated complications. MD can be a large base or a narrow base, with a mesodiverticular band but the diverticulum is usually a blind recess. In our case, the tube connected two intestinal segments. To the best of our knowledge, we have reported the first case of an MD-like permeable tube with a double basis.

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双基性梅克尔憩室继发机械性小肠梗阻的腹腔镜治疗。罕见的解剖表现。
梅克尔憩室(MD)是最常见的先天性胃肠道异常。MD引起的肠阻塞是肠套叠或肠扭转的常见后果。在这里,我们报告一个11岁的男孩谁提出了急诊科急性腹痛,胆汁性呕吐,腹部反跳压痛。计算机断层扫描诊断为肠道闭塞,没有明显的原因。患者接受诊断性腹腔镜检查,确定双基渗透性Meckel机械闭塞。通过吻合器进行憩室切除术,缓解了闭塞。MD是一种罕见的疾病(仅占普通人群的0.3-2.9%),只有4.2 - 9%的MD患者有相关并发症。MD可为大基底或窄基底,伴憩室系带,但憩室通常为盲隐窝。在我们的病例中,管子连接了两个肠段。据我们所知,我们已经报道了第一例具有双重基底的md样可渗透管。
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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