Fibrous solitary tumor, a rare and ubiquitous neoplasy

Fibrous solitary tumors (FST) are mesenchymal tumors that can appear in different body regions. It is estimated that around 30% are found in the thoracic region, while rarely in meninges, abdomen, pelvis, extremities and bones. A correct diagnosis is important because 15–20% of cases develop a malig...

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Autores principales: Ros, Alejandro, Cortés, Javier, Belda, Tatiana, Magán, Alejandro, Illán-Gambín, Francisco J, Aracil, Elisa, Serra, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304934/
https://www.ncbi.nlm.nih.gov/pubmed/32587681
http://dx.doi.org/10.1093/jscr/rjaa156
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author Ros, Alejandro
Cortés, Javier
Belda, Tatiana
Magán, Alejandro
Illán-Gambín, Francisco J
Aracil, Elisa
Serra, Carlos
author_facet Ros, Alejandro
Cortés, Javier
Belda, Tatiana
Magán, Alejandro
Illán-Gambín, Francisco J
Aracil, Elisa
Serra, Carlos
author_sort Ros, Alejandro
collection PubMed
description Fibrous solitary tumors (FST) are mesenchymal tumors that can appear in different body regions. It is estimated that around 30% are found in the thoracic region, while rarely in meninges, abdomen, pelvis, extremities and bones. A correct diagnosis is important because 15–20% of cases develop a malignant behavior. Treatment of choice is surgical and posterior follow-up is essential. We present two atypical extrapleural FST cases, diagnosed in our center. Both were treated with surgery and in one case arterial embolization to reduce the bleeding risk was previously done.
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spelling pubmed-73049342020-06-24 Fibrous solitary tumor, a rare and ubiquitous neoplasy Ros, Alejandro Cortés, Javier Belda, Tatiana Magán, Alejandro Illán-Gambín, Francisco J Aracil, Elisa Serra, Carlos J Surg Case Rep Case Report Fibrous solitary tumors (FST) are mesenchymal tumors that can appear in different body regions. It is estimated that around 30% are found in the thoracic region, while rarely in meninges, abdomen, pelvis, extremities and bones. A correct diagnosis is important because 15–20% of cases develop a malignant behavior. Treatment of choice is surgical and posterior follow-up is essential. We present two atypical extrapleural FST cases, diagnosed in our center. Both were treated with surgery and in one case arterial embolization to reduce the bleeding risk was previously done. Oxford University Press 2020-06-18 /pmc/articles/PMC7304934/ /pubmed/32587681 http://dx.doi.org/10.1093/jscr/rjaa156 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2020. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Ros, Alejandro
Cortés, Javier
Belda, Tatiana
Magán, Alejandro
Illán-Gambín, Francisco J
Aracil, Elisa
Serra, Carlos
Fibrous solitary tumor, a rare and ubiquitous neoplasy
title Fibrous solitary tumor, a rare and ubiquitous neoplasy
title_full Fibrous solitary tumor, a rare and ubiquitous neoplasy
title_fullStr Fibrous solitary tumor, a rare and ubiquitous neoplasy
title_full_unstemmed Fibrous solitary tumor, a rare and ubiquitous neoplasy
title_short Fibrous solitary tumor, a rare and ubiquitous neoplasy
title_sort fibrous solitary tumor, a rare and ubiquitous neoplasy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304934/
https://www.ncbi.nlm.nih.gov/pubmed/32587681
http://dx.doi.org/10.1093/jscr/rjaa156
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