{"title":"【孤立性肠系膜纤维瘤病】。","authors":"M Flesch, A Low, A Hirner, H Vetter","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Isolated mesenteric fibromatosis is a rare form from the group of intraabdominal fibromatoses which often accompany Gardner's syndrome. It consists in a benign proliferation of fibroblasts with infiltration of muscles and fat tissue. It is diagnosed by ultrasound and CT-scans. The treatment of choice is the total surgical extirpation of the tumor. We report about a 19 year old patient with an isolated mesenteric fibromatosis following a normal pregnancy without previous surgical interventions.</p>","PeriodicalId":21438,"journal":{"name":"Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis","volume":"83 22","pages":"684-6"},"PeriodicalIF":0.0000,"publicationDate":"1994-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Isolated mesenteric fibromatosis].\",\"authors\":\"M Flesch, A Low, A Hirner, H Vetter\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Isolated mesenteric fibromatosis is a rare form from the group of intraabdominal fibromatoses which often accompany Gardner's syndrome. It consists in a benign proliferation of fibroblasts with infiltration of muscles and fat tissue. It is diagnosed by ultrasound and CT-scans. The treatment of choice is the total surgical extirpation of the tumor. We report about a 19 year old patient with an isolated mesenteric fibromatosis following a normal pregnancy without previous surgical interventions.</p>\",\"PeriodicalId\":21438,\"journal\":{\"name\":\"Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis\",\"volume\":\"83 22\",\"pages\":\"684-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1994-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Isolated mesenteric fibromatosis is a rare form from the group of intraabdominal fibromatoses which often accompany Gardner's syndrome. It consists in a benign proliferation of fibroblasts with infiltration of muscles and fat tissue. It is diagnosed by ultrasound and CT-scans. The treatment of choice is the total surgical extirpation of the tumor. We report about a 19 year old patient with an isolated mesenteric fibromatosis following a normal pregnancy without previous surgical interventions.
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