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A series of two cases of rare tumors: Solitary fibrous tumor of the pleura

Solitary fibrous tumors of the pleura (SFTPs) are rare neoplasms of mesenchymal origin most commonly arising in the pleura and have a benign biological behavior in the majority of cases. Most patients with SFTPs are asymptomatic; however, symptoms are mostly related to the mass effect within the tho...

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Autores principales: Bukamur, Hazim, Karem, Emhemmid, Fares, Serag, Sigdel, Saroj, Alkhankan, Emad, Zeid, Fuad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554494/
https://www.ncbi.nlm.nih.gov/pubmed/31194146
http://dx.doi.org/10.1016/j.rmcr.2019.100872
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author Bukamur, Hazim
Karem, Emhemmid
Fares, Serag
Sigdel, Saroj
Alkhankan, Emad
Zeid, Fuad
author_facet Bukamur, Hazim
Karem, Emhemmid
Fares, Serag
Sigdel, Saroj
Alkhankan, Emad
Zeid, Fuad
author_sort Bukamur, Hazim
collection PubMed
description Solitary fibrous tumors of the pleura (SFTPs) are rare neoplasms of mesenchymal origin most commonly arising in the pleura and have a benign biological behavior in the majority of cases. Most patients with SFTPs are asymptomatic; however, symptoms are mostly related to the mass effect within the thoracic cavity. Chest computed tomography (CT) scanning is the radiographic test of choice, but findings lack specificity. Surgical resection is the treatment of choice for most patients. Long-term survival after resection of benign SFTPs is excellent. In this case series, we present two females, one presented with shortness of breath (SOB) and nonproductive cough and the other one was referred because of abnormal x-ray findings. The histological as well as the immunohistochemical examination revealed the mass to be a solitary fibrous tumor of the pleura.
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spelling pubmed-65544942019-06-10 A series of two cases of rare tumors: Solitary fibrous tumor of the pleura Bukamur, Hazim Karem, Emhemmid Fares, Serag Sigdel, Saroj Alkhankan, Emad Zeid, Fuad Respir Med Case Rep Case Report Solitary fibrous tumors of the pleura (SFTPs) are rare neoplasms of mesenchymal origin most commonly arising in the pleura and have a benign biological behavior in the majority of cases. Most patients with SFTPs are asymptomatic; however, symptoms are mostly related to the mass effect within the thoracic cavity. Chest computed tomography (CT) scanning is the radiographic test of choice, but findings lack specificity. Surgical resection is the treatment of choice for most patients. Long-term survival after resection of benign SFTPs is excellent. In this case series, we present two females, one presented with shortness of breath (SOB) and nonproductive cough and the other one was referred because of abnormal x-ray findings. The histological as well as the immunohistochemical examination revealed the mass to be a solitary fibrous tumor of the pleura. Elsevier 2019-06-04 /pmc/articles/PMC6554494/ /pubmed/31194146 http://dx.doi.org/10.1016/j.rmcr.2019.100872 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Bukamur, Hazim
Karem, Emhemmid
Fares, Serag
Sigdel, Saroj
Alkhankan, Emad
Zeid, Fuad
A series of two cases of rare tumors: Solitary fibrous tumor of the pleura
title A series of two cases of rare tumors: Solitary fibrous tumor of the pleura
title_full A series of two cases of rare tumors: Solitary fibrous tumor of the pleura
title_fullStr A series of two cases of rare tumors: Solitary fibrous tumor of the pleura
title_full_unstemmed A series of two cases of rare tumors: Solitary fibrous tumor of the pleura
title_short A series of two cases of rare tumors: Solitary fibrous tumor of the pleura
title_sort series of two cases of rare tumors: solitary fibrous tumor of the pleura
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554494/
https://www.ncbi.nlm.nih.gov/pubmed/31194146
http://dx.doi.org/10.1016/j.rmcr.2019.100872
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