Giant pelvic solitary fibrous tumor. Presentation of a rare case

Solitary fibrous tumors (STFs) consist a very rare and unique group of neoplasms throughout the entire human system. Basic histopathologic origin represents the mesenchymal tissue with slight exceptions. Major incidence obtains the pleura with anatomic occupations especially in the limps, necks and gastrointestinal tracts. Surgical dissection represents the gold standard of therapeutic strategy. According to recent bibliography, only a few cases have been described arising from anatomic areas from mesentery and colon. Aim of our study consists the presentation of such rare tumor group accompanied with assiduous diagnosis and therapeutic mapping.