Mesenteric fibromatosis with intestinal involvement mimicking a gastrointestinal stromal tumour

Authors

  • Marek Wronski
  • Bogna Ziarkiewicz-Wroblewska
  • Maciej Slodkowski
  • Wlodzimierz Cebulski
  • Barbara Gornicka
  • Ireneusz W. Krasnodebski

Abstract

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.

Author Biographies

Marek Wronski

Bogna Ziarkiewicz-Wroblewska

Maciej Slodkowski

Wlodzimierz Cebulski

Barbara Gornicka

Ireneusz W. Krasnodebski

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Published

2011-03-01

How to Cite

Wronski, M., Ziarkiewicz-Wroblewska, B., Slodkowski, M., Cebulski, W., Gornicka, B., & Krasnodebski, I. W. (2011). Mesenteric fibromatosis with intestinal involvement mimicking a gastrointestinal stromal tumour. Radiology and Oncology, 45(1). Retrieved from https://www.radioloncol.com/index.php/ro/article/view/1086

Issue

Section

Clinical oncology