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...

Full description

Bibliographic Details
Main Authors: Karim M. Eltawil, Carly Whalen, Bryce Knapp
Format: Article
Language:English
Published: SpringerOpen 2021-04-01
Series:Surgical Case Reports
Subjects:
Online Access:https://doi.org/10.1186/s40792-021-01176-w
id doaj-71f63ccb2ecd4526aa90d0defe310deb
record_format Article
spelling 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
work_keys_str_mv AT karimmeltawil solitaryfibroustumorofthegreateromentumcasereportandreviewofliterature
AT carlywhalen solitaryfibroustumorofthegreateromentumcasereportandreviewofliterature
AT bryceknapp solitaryfibroustumorofthegreateromentumcasereportandreviewofliterature
_version_ 1721522391708860416