Massive bleeding with intussusception due to Meckel's diverticulum: a case report.

E. Açoğlu, G. Yilmaz, Aytaç Kenar, A. Karaman, F. O. Hoşnut, Nazlı Altun Yoloğlu, S. Apaydın, G. Çınar
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引用次数: 0

Abstract

Meckel’s diverticulum is the most common congenital anomaly of the gastrointestinal tract. It is originated from nonclosure of omphalomesenteric tube between 5-7th intrauterine week. Most cases of Meckel’s diverticula are asymptomatic. This pathologic lesion could lead to intestinal obstruction and bleeding, life threatening and can cause acute abdomen which mandatory laparatomy during childhood. The diagnosis of symptomatic Meckel’s diverticulum is often difficult to make. Here, we report a case of a one-year-old boy presented with recurrent life-threatening lower gastrointestinal bleeding and Meckel’s diverticulum with intussusception was diagnosed result of the operation and review the literature for difficulties in identifying.
梅克尔憩室致肠套叠大出血1例。
梅克尔憩室是胃肠道最常见的先天性异常。它起源于子宫内5-7周时输卵管不闭合。大多数梅克尔憩室是无症状的。这种病理病变可导致肠梗阻和出血,危及生命,并可引起急腹症,在儿童时期必须进行腹腔镜手术。症状性梅克尔憩室的诊断通常是困难的。在此,我们报告一名一岁男童复发性危及生命的下消化道出血,手术后诊断为梅克尔憩室伴肠套叠,并回顾文献中难以识别的病例。
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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