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Extrapleural solitary fibrous tumor—a revision of three cases
Extrapleural solitary fibrous tumors are a rare type of spindle cell neoplasm, which can occur in many locations with different histologic and immunohistochemical findings, making the diagnosis challenging. They are usually indolent and their treatment is based on complete surgical resection. There...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049790/ https://www.ncbi.nlm.nih.gov/pubmed/36998260 http://dx.doi.org/10.1093/jscr/rjad151 |
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author | Policarpo, Filipa Rafael, Ana Alves Teixeira, José Nuno Chorão, Martinha |
author_facet | Policarpo, Filipa Rafael, Ana Alves Teixeira, José Nuno Chorão, Martinha |
author_sort | Policarpo, Filipa |
collection | PubMed |
description | Extrapleural solitary fibrous tumors are a rare type of spindle cell neoplasm, which can occur in many locations with different histologic and immunohistochemical findings, making the diagnosis challenging. They are usually indolent and their treatment is based on complete surgical resection. There are still some issues to be clarified regarding systemic therapy (specifically when aggressive behavior exists) and long-term follow-up. We present a series of clinical cases in the same Department and review this thematic area. |
format | Online Article Text |
id | pubmed-10049790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100497902023-03-29 Extrapleural solitary fibrous tumor—a revision of three cases Policarpo, Filipa Rafael, Ana Alves Teixeira, José Nuno Chorão, Martinha J Surg Case Rep Case Series Extrapleural solitary fibrous tumors are a rare type of spindle cell neoplasm, which can occur in many locations with different histologic and immunohistochemical findings, making the diagnosis challenging. They are usually indolent and their treatment is based on complete surgical resection. There are still some issues to be clarified regarding systemic therapy (specifically when aggressive behavior exists) and long-term follow-up. We present a series of clinical cases in the same Department and review this thematic area. Oxford University Press 2023-03-28 /pmc/articles/PMC10049790/ /pubmed/36998260 http://dx.doi.org/10.1093/jscr/rjad151 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2023. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Series Policarpo, Filipa Rafael, Ana Alves Teixeira, José Nuno Chorão, Martinha Extrapleural solitary fibrous tumor—a revision of three cases |
title | Extrapleural solitary fibrous tumor—a revision of three cases |
title_full | Extrapleural solitary fibrous tumor—a revision of three cases |
title_fullStr | Extrapleural solitary fibrous tumor—a revision of three cases |
title_full_unstemmed | Extrapleural solitary fibrous tumor—a revision of three cases |
title_short | Extrapleural solitary fibrous tumor—a revision of three cases |
title_sort | extrapleural solitary fibrous tumor—a revision of three cases |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049790/ https://www.ncbi.nlm.nih.gov/pubmed/36998260 http://dx.doi.org/10.1093/jscr/rjad151 |
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