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Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report
Although a solitary fibrous tumor of the pleura (SFTP) is a rare disease, and usually has a benign course, it has a malignant potential. We report a case of malignant SFTP treated surgically. A 75- year-old female was admitted with a chief complaint of hemoptysis of two weeks duration. Computed tomo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078939/ https://www.ncbi.nlm.nih.gov/pubmed/24952611 http://dx.doi.org/10.1186/1749-8090-9-113 |
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author | Jeon, Hyun Woo Kwon, Soon Seog Kim, Young-Du |
author_facet | Jeon, Hyun Woo Kwon, Soon Seog Kim, Young-Du |
author_sort | Jeon, Hyun Woo |
collection | PubMed |
description | Although a solitary fibrous tumor of the pleura (SFTP) is a rare disease, and usually has a benign course, it has a malignant potential. We report a case of malignant SFTP treated surgically. A 75- year-old female was admitted with a chief complaint of hemoptysis of two weeks duration. Computed tomography of the chest imaged a large mass in the right hemithorax, which compressed adjacent organs; however, there was no evidence of invasion. We reviewed the patient’s medical records and found that the mass had been presented for 17 years. Complete resection was achieved through a right thoracotomy and histopathologic examination confirmed a malignant SFTP. |
format | Online Article Text |
id | pubmed-4078939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40789392014-07-03 Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report Jeon, Hyun Woo Kwon, Soon Seog Kim, Young-Du J Cardiothorac Surg Case Report Although a solitary fibrous tumor of the pleura (SFTP) is a rare disease, and usually has a benign course, it has a malignant potential. We report a case of malignant SFTP treated surgically. A 75- year-old female was admitted with a chief complaint of hemoptysis of two weeks duration. Computed tomography of the chest imaged a large mass in the right hemithorax, which compressed adjacent organs; however, there was no evidence of invasion. We reviewed the patient’s medical records and found that the mass had been presented for 17 years. Complete resection was achieved through a right thoracotomy and histopathologic examination confirmed a malignant SFTP. BioMed Central 2014-06-21 /pmc/articles/PMC4078939/ /pubmed/24952611 http://dx.doi.org/10.1186/1749-8090-9-113 Text en Copyright © 2014 Jeon et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Jeon, Hyun Woo Kwon, Soon Seog Kim, Young-Du Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report |
title | Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report |
title_full | Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report |
title_fullStr | Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report |
title_full_unstemmed | Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report |
title_short | Malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report |
title_sort | malignant solitary fibrous tumor of the pleura slowly growing over 17 years: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078939/ https://www.ncbi.nlm.nih.gov/pubmed/24952611 http://dx.doi.org/10.1186/1749-8090-9-113 |
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