Mesenteric fibromatosis with intestinal involvement mimicking a gastrointestinal stromal tumour

被引:23
|
作者
Wronski, Marek [1 ]
Ziarkiewicz-Wroblewska, Bogna [2 ]
Slodkowski, Maciej [1 ]
Cebulski, Wlodzimierz [1 ]
Gornicka, Barbara [2 ]
Krasnodebski, Ireneusz W. [1 ]
机构
[1] Med Univ Warsaw, Dept Gen Gastroenterol & Oncol Surg, Warsaw, Poland
[2] Med Univ Warsaw, Dept Pathol, Warsaw, Poland
关键词
mesenteric fibromatosis; desmoid tumour; gastrointestinal stromal tumour; GIST; differential diagnosis; FAMILIAL ADENOMATOUS POLYPOSIS; DESMOID TUMORS; PATHOLOGICAL CORRELATION; AGGRESSIVE FIBROMATOSIS; LESIONS; CANCER; BENIGN; GIST;
D O I
10.2478/v10019-010-0051-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction. Mesenteric fibromatosis or intra-abdominal desmoid tumour is a rare proliferative disease affecting the mesentery. It is a locally aggressive tumour that lacks metastatic potential, but the local recurrence is common. Mesenteric fibromatosis with the intestinal involvement can be easily confused with other primary gastrointestinal tumours, especially with that of the mesenchymal origin. Case report. We report a case of a 44-year-old female who presented with an abdominal mass that radiologically and pathologically mimicked a gastrointestinal stromal tumour. Conclusions. The diagnosis of mesenteric fibromatosis should always be considered in the case of mesenchymal tumours apparently originating from the bowel wall that diffusely infiltrate the mesentery.
引用
收藏
页码:59 / 63
页数:5
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