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Primary Synovial Sarcoma of Lung

Synovial sarcoma (SS) is a highly malignant tumor that accounts for 10% of all soft-tissue sarcomas. Primary SS arising from the lung is extremely rare, and the prognosis is poor. We report a case of pulmonary SS presenting with a mass lesion invading the right upper and middle lobes, extending to t...

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Autores principales: Cabuk, Devrim, Ustuner, Berna, Akgul, Asli Gul, Acikgoz, Ozgur, Yaprak, Busra, Uygun, Kazim, Topcu, Salih, Muezzinoglu, Bahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157487/
https://www.ncbi.nlm.nih.gov/pubmed/25207234
http://dx.doi.org/10.5090/kjtcs.2014.47.3.306
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author Cabuk, Devrim
Ustuner, Berna
Akgul, Asli Gul
Acikgoz, Ozgur
Yaprak, Busra
Uygun, Kazim
Topcu, Salih
Muezzinoglu, Bahar
author_facet Cabuk, Devrim
Ustuner, Berna
Akgul, Asli Gul
Acikgoz, Ozgur
Yaprak, Busra
Uygun, Kazim
Topcu, Salih
Muezzinoglu, Bahar
author_sort Cabuk, Devrim
collection PubMed
description Synovial sarcoma (SS) is a highly malignant tumor that accounts for 10% of all soft-tissue sarcomas. Primary SS arising from the lung is extremely rare, and the prognosis is poor. We report a case of pulmonary SS presenting with a mass lesion invading the right upper and middle lobes, extending to the mediastinum and the chest wall. After tru-cut biopsy, surgical resection was performed. The final diagnosis was SS (biphasic type) based on histological and immunohistochemical findings. There are no guidelines for optimal treatment due to the rarity of these tumors. Current treatment includes surgery and adjuvant chemotherapy and/or radiotherapy.
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spelling pubmed-41574872014-09-09 Primary Synovial Sarcoma of Lung Cabuk, Devrim Ustuner, Berna Akgul, Asli Gul Acikgoz, Ozgur Yaprak, Busra Uygun, Kazim Topcu, Salih Muezzinoglu, Bahar Korean J Thorac Cardiovasc Surg Case Report Synovial sarcoma (SS) is a highly malignant tumor that accounts for 10% of all soft-tissue sarcomas. Primary SS arising from the lung is extremely rare, and the prognosis is poor. We report a case of pulmonary SS presenting with a mass lesion invading the right upper and middle lobes, extending to the mediastinum and the chest wall. After tru-cut biopsy, surgical resection was performed. The final diagnosis was SS (biphasic type) based on histological and immunohistochemical findings. There are no guidelines for optimal treatment due to the rarity of these tumors. Current treatment includes surgery and adjuvant chemotherapy and/or radiotherapy. The Korean Society for Thoracic and Cardiovascular Surgery 2014-06 2014-06-05 /pmc/articles/PMC4157487/ /pubmed/25207234 http://dx.doi.org/10.5090/kjtcs.2014.47.3.306 Text en Copyright © 2014 by The Korean Society for Thoracic and Cardiovascular Surgery. All rights Reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Cabuk, Devrim
Ustuner, Berna
Akgul, Asli Gul
Acikgoz, Ozgur
Yaprak, Busra
Uygun, Kazim
Topcu, Salih
Muezzinoglu, Bahar
Primary Synovial Sarcoma of Lung
title Primary Synovial Sarcoma of Lung
title_full Primary Synovial Sarcoma of Lung
title_fullStr Primary Synovial Sarcoma of Lung
title_full_unstemmed Primary Synovial Sarcoma of Lung
title_short Primary Synovial Sarcoma of Lung
title_sort primary synovial sarcoma of lung
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157487/
https://www.ncbi.nlm.nih.gov/pubmed/25207234
http://dx.doi.org/10.5090/kjtcs.2014.47.3.306
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