Open AccessRadiological findings in pelvic solitary fibrous tumour
Author(s) -
Paul Johannet,
Aya Kamaya,
Gabriela Gayer
Publication year - 2016
Publication title -
bjr case reports
Language(s) - English
Resource type - Journals
ISSN - 2055-7159
DOI - 10.1259/bjrcr.20150373
Subject(s) - medicine , solitary fibrous tumor , pelvis , radiology , abdomen , radiological weapon , ultrasound , pelvic cavity , genetics , stem cell , cd34 , biology
Solitary fibrous tumour (SFT) is an uncommon, usually benign mesenchymal neoplasm. SFT was first described in the pleura, but has subsequently been reported to occur in numerous anatomic locations including the abdomen and pelvis. Abdominopelvic SFTs are typically an indolent process, in spite of reaching a large size by the time of diagnosis. The preferred treatment is complete resection followed by extended follow-up surveillance. The risk of local recurrence and metastasis correlates with tumour size and the histological status of surgical margins. We present the imaging findings of a large pelvic SFT in a 61-year-old female, including ultrasound, CT and MRI.