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 in | The Korean journal of medicine Vol. 54; no. 4; pp. 577 - 581 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | Korean |
Published |
대한내과학회
01.04.1998
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Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | The Korean Association Of Internal Medicine |
ISSN: | 1738-9364 |