충수정제술 후 발생한 장간막 섬유종증

Mesenteric fibromatosis is a rare nonmetastasizing fibrous tumor, characterized by fibroblastic proliferation without evidence of inflammatory response or definite neoplasia. It appears at any age, but mainly in the second to fifth decades as incidence of two to four desmoid tumor cases per 1 rnilli...

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Published inThe Korean journal of medicine Vol. 54; no. 4; pp. 577 - 581
Main Authors 남근하, Keun Ha Nam, 권범찬, Bum Chan Kweon, 이한균, Han Kyun Lee, 이동욱, Dong Wook Lee, 권소정, So Jung Kweon, 우창근, Chang Keun Woo, 박진석, Jin Seouk Park, 황중하, Joong Ha Hwang, 이중기, Choong Ki Lee
Format Journal Article
LanguageKorean
Published 대한내과학회 01.04.1998
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Summary:Mesenteric fibromatosis is a rare nonmetastasizing fibrous tumor, characterized by fibroblastic proliferation without evidence of inflammatory response or definite neoplasia. It appears at any age, but mainly in the second to fifth decades as incidence of two to four desmoid tumor cases per 1 rnillion people per annum. It is pseudoencapsulated and locally invasive and has a tendency to recur, but metastases are rare. It is more frequent with Gardner`s syndrome(adenomatosis coli) in which 50% of them will appear as mesenteric fibromatosis. Trauma, especially that of previous surgery, has been associated with the subsequent development of desmoid tumor. The treatment of choice is a wide margin resection of the tumor. we experienced a case of mesenteric fibromatosis without Gardner`s syndrome 2 years after appendectomy in a 31-year old man and recurred at 21 months after resection and report with a review of literatures.
Bibliography:The Korean Association Of Internal Medicine
ISSN:1738-9364