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一例梅克尔憩室合并结肠狭窄的病例。

A case of Meckel's diverticulum complicated by stenosis of the colon.

作者信息

Akamine M, Araki Y, Chijiiwa Y, Shimizu S, Shimura H, Nawata H

机构信息

Third Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Am J Gastroenterol. 1997 Nov;92(11):2114-6.

PMID:9362206
Abstract

Meckel's diverticulum is a common anomaly of the GI tract that is known to cause small intestinal obstruction. A 17-yr-old male who had no history of previous surgery was admitted with intermittent abdominal pain. A barium enema showed extraintestinal compression of the ascending colon, suggesting the existence of a congenital band. Laparoscopy revealed that the ascending colon was lifted up and compressed by the intestinal end of a Meckel's diverticulum with a fibrous band connecting to the umbilicus. The portion of the ileum including the Meckel's diverticulum was resected. This is the first case of stenosis of the colon caused by a Meckel's diverticulum.

摘要

梅克尔憩室是胃肠道常见的先天性异常,已知可导致小肠梗阻。一名17岁无既往手术史的男性因间歇性腹痛入院。钡剂灌肠显示升结肠有肠外压迫,提示存在先天性束带。腹腔镜检查发现升结肠被梅克尔憩室的肠端抬起并压迫,有一条纤维带连接至脐部。切除包括梅克尔憩室的回肠部分。这是首例由梅克尔憩室导致的结肠狭窄病例。

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