Solitary fibrous tumor of the greater omentum: case report and review of literature
Abstract Background Solitary fibrous tumor (SFT) is a rare neoplasm of mesenchymal origin occurring most often in the visceral pleura, however, it has been described in almost every anatomic location of the human body. While most SFTs have a benign behavior, they can potentially be locally aggressiv...
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doaj-71f63ccb2ecd4526aa90d0defe310deb2021-04-18T11:21:55ZengSpringerOpenSurgical Case Reports2198-77932021-04-01711610.1186/s40792-021-01176-wSolitary fibrous tumor of the greater omentum: case report and review of literatureKarim M. Eltawil0Carly Whalen1Bryce Knapp2Department of Surgery, La Verendrye General Hospital, Riverside Health Care FacilitiesDepartment of Surgery, La Verendrye General Hospital, Riverside Health Care FacilitiesNorthern Ontario School of MedicineAbstract Background Solitary fibrous tumor (SFT) is a rare neoplasm of mesenchymal origin occurring most often in the visceral pleura, however, it has been described in almost every anatomic location of the human body. While most SFTs have a benign behavior, they can potentially be locally aggressive and demonstrate a malignant behavior. Case presentation A 63 year-old male patient presented with lower abdominal pain and nausea and was noted on CT to have a large, heterogeneous lower abdominal mass with no evidence of metastatic disease. A surgical resection was performed and the mass appeared to be connected to the greater omentum with a vascular pedicle. It was not invading any intra-abdominal or pelvic organs. Pathology revealed an SFT of omental origin. The mitotic count was less than 4 per 10 high-power fields and all pathologic characteristics did not meet the criteria for a malignant SFT. Conclusions We report an extremely rare case of SFT originating from the greater omentum. A multidisciplinary team approach was followed to plan the patient’s management strategy.https://doi.org/10.1186/s40792-021-01176-wSolitary fibrous tumorOmentumSurgical resection |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Karim M. Eltawil Carly Whalen Bryce Knapp |
spellingShingle |
Karim M. Eltawil Carly Whalen Bryce Knapp Solitary fibrous tumor of the greater omentum: case report and review of literature Surgical Case Reports Solitary fibrous tumor Omentum Surgical resection |
author_facet |
Karim M. Eltawil Carly Whalen Bryce Knapp |
author_sort |
Karim M. Eltawil |
title |
Solitary fibrous tumor of the greater omentum: case report and review of literature |
title_short |
Solitary fibrous tumor of the greater omentum: case report and review of literature |
title_full |
Solitary fibrous tumor of the greater omentum: case report and review of literature |
title_fullStr |
Solitary fibrous tumor of the greater omentum: case report and review of literature |
title_full_unstemmed |
Solitary fibrous tumor of the greater omentum: case report and review of literature |
title_sort |
solitary fibrous tumor of the greater omentum: case report and review of literature |
publisher |
SpringerOpen |
series |
Surgical Case Reports |
issn |
2198-7793 |
publishDate |
2021-04-01 |
description |
Abstract Background Solitary fibrous tumor (SFT) is a rare neoplasm of mesenchymal origin occurring most often in the visceral pleura, however, it has been described in almost every anatomic location of the human body. While most SFTs have a benign behavior, they can potentially be locally aggressive and demonstrate a malignant behavior. Case presentation A 63 year-old male patient presented with lower abdominal pain and nausea and was noted on CT to have a large, heterogeneous lower abdominal mass with no evidence of metastatic disease. A surgical resection was performed and the mass appeared to be connected to the greater omentum with a vascular pedicle. It was not invading any intra-abdominal or pelvic organs. Pathology revealed an SFT of omental origin. The mitotic count was less than 4 per 10 high-power fields and all pathologic characteristics did not meet the criteria for a malignant SFT. Conclusions We report an extremely rare case of SFT originating from the greater omentum. A multidisciplinary team approach was followed to plan the patient’s management strategy. |
topic |
Solitary fibrous tumor Omentum Surgical resection |
url |
https://doi.org/10.1186/s40792-021-01176-w |
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