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Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site
Extrapleural solitary fibrous tumor-hemangiopericytoma is a rare tumor. We present a case of this tumor arising in omentum, which is an extremely rare site. The diagnosis was confirmed by diffuse expression of STAT6 on immunohistochemistry. The tumor was assigned a low-risk category according to rec...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Medical and Scientific Publishers Pvt. Ltd.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478505/ https://www.ncbi.nlm.nih.gov/pubmed/34602796 http://dx.doi.org/10.1055/s-0041-1731942 |
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author | Ingle, Abhijeet Reddy, Surender Reddy, Vamshi Krishna |
author_facet | Ingle, Abhijeet Reddy, Surender Reddy, Vamshi Krishna |
author_sort | Ingle, Abhijeet |
collection | PubMed |
description | Extrapleural solitary fibrous tumor-hemangiopericytoma is a rare tumor. We present a case of this tumor arising in omentum, which is an extremely rare site. The diagnosis was confirmed by diffuse expression of STAT6 on immunohistochemistry. The tumor was assigned a low-risk category according to recent risk categorization models. The patient was advised close follow-up as the tumor was excised completely. These tumors have the potential for recurrence and metastasis even after surgical excision. However, there are no definitive guidelines for adjuvant treatment due to lack of data. |
format | Online Article Text |
id | pubmed-8478505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Thieme Medical and Scientific Publishers Pvt. Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84785052021-10-01 Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site Ingle, Abhijeet Reddy, Surender Reddy, Vamshi Krishna J Lab Physicians Extrapleural solitary fibrous tumor-hemangiopericytoma is a rare tumor. We present a case of this tumor arising in omentum, which is an extremely rare site. The diagnosis was confirmed by diffuse expression of STAT6 on immunohistochemistry. The tumor was assigned a low-risk category according to recent risk categorization models. The patient was advised close follow-up as the tumor was excised completely. These tumors have the potential for recurrence and metastasis even after surgical excision. However, there are no definitive guidelines for adjuvant treatment due to lack of data. Thieme Medical and Scientific Publishers Pvt. Ltd. 2021-09 2021-07-09 /pmc/articles/PMC8478505/ /pubmed/34602796 http://dx.doi.org/10.1055/s-0041-1731942 Text en The Indian Association of Laboratory Physicians. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Ingle, Abhijeet Reddy, Surender Reddy, Vamshi Krishna Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site |
title | Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site |
title_full | Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site |
title_fullStr | Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site |
title_full_unstemmed | Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site |
title_short | Omental Solitary Fibrous Tumor: A Rare Tumor at Rare Site |
title_sort | omental solitary fibrous tumor: a rare tumor at rare site |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478505/ https://www.ncbi.nlm.nih.gov/pubmed/34602796 http://dx.doi.org/10.1055/s-0041-1731942 |
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