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Congenital mesocolic hernia is a rare disease which resulted from abnormal rotation of midgut during development period. It is classified by the site of mesocolic defect and hernia sac. The transverse mesocolic hernia is extremely rare. A 57-years-old man was admitted due to nausea, epigastric pain...

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Published inThe Korean journal of gastroenterology Vol. 33; no. 4; pp. 557 - 561
Main Authors 이인석, In Seok Lee, 오귀염, Guy Yum Oh, 최황, Hwang Choi, 양진모, Jin Mo Yang, 김재광, Jae Kwang Kim, 최명규, Myong Gyu Choi, 정규원, Kyu Won Chung, 선희식, Hee Si k Sun, 김원우, Won Woo Ki m, 김승남, Seung Nam Kim, 정승은, Seung Eun Jung
Format Journal Article
LanguageKorean
Published 대한소화기학회 01.01.1999
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Summary:Congenital mesocolic hernia is a rare disease which resulted from abnormal rotation of midgut during development period. It is classified by the site of mesocolic defect and hernia sac. The transverse mesocolic hernia is extremely rare. A 57-years-old man was admitted due to nausea, epigastric pain and abdominal distension. He had been diagnosed as duodenal ulcer with pyloric deformity 18 months ago. Simple abdomen X-ray with gastrografin swallowing and abdominal CT highly suggested internal hernia. Surgical exploration was done under the diagnosis of internal hernia. There was a 3 cm sized defect at transverse mesocolon and nearly total small intestine, which was herniated into the lesser sac and retroperitoneal space without strangulation. After simple resection of transverse mesocolic defect and transverse colon, reduction of herniated bowel and simple closure of transverse colon were done. (Kor J Gastroenterol 1999;33:557 - 561)
Bibliography:Korean Society of Gastroenterology
ISSN:1598-9992