The Desmoid Tumor Research Foundation

January 2017

Desmoid-type Fibromatosis of the Mesentery: A Case Report

Author Information

Tatyana M. Betova, Savelina L. Popovska, Radoslav G. Trifonov(1), Konstantina S. Karakadieva(1), Genoveva B. Valcheva(2), Lachezar S. Tanchev(3)

Department of Patholoanatomy, Medical University Ð Pleven, Bulgaria(1)Student of Medical University Ð Pleven, Bulgaria(2)Division of Oncological Surgery, Oncology Center, Medical University Ð Pleven, Bulgaria(3)Division of Gynecologic Oncology, Oncology Center, Medical University Ð Pleven, Bulgaria

Publication

J Biomed Clin Res

Summary

According to their anatomical position, desmoid-type fibromatoses can be divided into three groups: extra- abdominal, intra-abdominal, and fibromatoses of the abdominal wall. Mesenteric fibromatoses account for 8% of the intra-abdominal ones. The latter are characterized by myofibroblastic proliferation and infiltration of both the pelvic and abdominal organs. We report a 26-year-old woman who complained of abdominal enlargement, feeling of heaviness, discomfort and reflux, which symptoms dated back 1-2 months prior to hospitalization. The patient underwent laparotomy due to subocclusive symptoms. Intraoperatively, a tumor sized 30 cm in diameter was found. The tumor originated from the mesentery and infiltrated in the jejunum, the entire ileum, and part of the caecum with perforation towards the abdominal cavity. The histological and immunohistochemical examinations are important for clarification of the diagnosis. The treatment requires a multidisciplinary approach, in which the surgical method has the key role.

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