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A Primary Synovial Sarcoma of Lung

Primary pulmonary synovial sarcoma is an extremely rare tumor. The diagnosis is established only after sarcoma like primary lung malignancies and metastatic sarcoma have been excluded. It has four subtypes: monophasic fibrous, monophasic epithelial, biphasic, and poorly differentiated subtypes, We r...

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Autores principales: Roy, PP, Das, A, Sarkar, A, Dwari, AK, Datta, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359438/
https://www.ncbi.nlm.nih.gov/pubmed/22655286
http://dx.doi.org/10.4103/1947-2714.95911
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author Roy, PP
Das, A
Sarkar, A
Dwari, AK
Datta, S
author_facet Roy, PP
Das, A
Sarkar, A
Dwari, AK
Datta, S
author_sort Roy, PP
collection PubMed
description Primary pulmonary synovial sarcoma is an extremely rare tumor. The diagnosis is established only after sarcoma like primary lung malignancies and metastatic sarcoma have been excluded. It has four subtypes: monophasic fibrous, monophasic epithelial, biphasic, and poorly differentiated subtypes, We report a case of a 55-year-old man, who complained of left-sided chest pain and shortness of breath, had a large heterogeneous mass, occupying most of left hemithorax, associated with ipsilateral pleural effusion, seen on contrast enhanced computed tomogram of thorax. Computed tomography guided tru-cut biopsy revealed spindle cell sarcoma. On immunohistochemistry, tumor cells expressed epithelial membrane antigen, CD99, bcl-2 and Calponin and were immunonegative for cytokeratin. So, final diagnosis was primary pulmonary synovial sarcoma, Primary pulmonary synovial sarcoma is a rarely reported case of malignant neoplasm of lung. Histopathology, immunohistochemistry, and cytogenetics, if possible, are essential for confirmation of its diagnosis.
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spelling pubmed-33594382012-05-31 A Primary Synovial Sarcoma of Lung Roy, PP Das, A Sarkar, A Dwari, AK Datta, S N Am J Med Sci Case Report Primary pulmonary synovial sarcoma is an extremely rare tumor. The diagnosis is established only after sarcoma like primary lung malignancies and metastatic sarcoma have been excluded. It has four subtypes: monophasic fibrous, monophasic epithelial, biphasic, and poorly differentiated subtypes, We report a case of a 55-year-old man, who complained of left-sided chest pain and shortness of breath, had a large heterogeneous mass, occupying most of left hemithorax, associated with ipsilateral pleural effusion, seen on contrast enhanced computed tomogram of thorax. Computed tomography guided tru-cut biopsy revealed spindle cell sarcoma. On immunohistochemistry, tumor cells expressed epithelial membrane antigen, CD99, bcl-2 and Calponin and were immunonegative for cytokeratin. So, final diagnosis was primary pulmonary synovial sarcoma, Primary pulmonary synovial sarcoma is a rarely reported case of malignant neoplasm of lung. Histopathology, immunohistochemistry, and cytogenetics, if possible, are essential for confirmation of its diagnosis. Medknow Publications & Media Pvt Ltd 2012-05 /pmc/articles/PMC3359438/ /pubmed/22655286 http://dx.doi.org/10.4103/1947-2714.95911 Text en Copyright: © North American Journal of Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Roy, PP
Das, A
Sarkar, A
Dwari, AK
Datta, S
A Primary Synovial Sarcoma of Lung
title A Primary Synovial Sarcoma of Lung
title_full A Primary Synovial Sarcoma of Lung
title_fullStr A Primary Synovial Sarcoma of Lung
title_full_unstemmed A Primary Synovial Sarcoma of Lung
title_short A Primary Synovial Sarcoma of Lung
title_sort primary synovial sarcoma of lung
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359438/
https://www.ncbi.nlm.nih.gov/pubmed/22655286
http://dx.doi.org/10.4103/1947-2714.95911
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