Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Obstetrics and Gynecology
Volume 2014 (2014), Article ID 906510, 4 pages
Case Report

Intraperitoneal Solitary Fibrous Tumor

1Department of Gynecology-Obstetric, Military Training Hospital Med V, Rabat, Morocco
2Faculty of Medicine and Pharmacy, University Mohammed V Souissi, Rabat, Morocco
3Department of Pathological Anatomy, Military Training Hospital Med V, Rabat, Morocco
4Department of Anesthesiology and Critical Care, Military Training Hospital Med V, Rabat, Morocco
5Department of Radiotherapy, Military Training Hospital Med V, Rabat, Morocco

Received 17 June 2014; Revised 10 August 2014; Accepted 11 August 2014; Published 7 September 2014

Academic Editor: Giampiero Capobianco

Copyright © 2014 Youssef Benabdejlil et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Solitary fibrous tumors of the pelvis are rare. We report the case of a 32-years-old patient who presented with abdominopelvic mass. The imaging studies showed a right adnexal mass of more than 10 cm. Exploratory laparotomy revealed a 20 cm mass at the Douglas pouch which was adhered to the posterior wall of the uterus. Complete resection of the mass was performed. Histological analysis showed a spindle cell undifferentiated tumor whose morphological and immunohistochemical profile are consistent with solitary fibrous tumor. It is important to know that although these tumors are rare, their evolution can be pejorative. Therefore, long-term followup should be recommended.