Primary Synovial Sarcoma of the Mediastinum : A Case Report

Synovial sarcomas commonly occur in the extremities of young adults. A primary occurrence in the mediastinum is very rare with only a few reported cases in the world literature. This paper is about a 42-year-old male who presented with chest pain and dyspnoea on exertion. Imaging showed an anteri...

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Main Authors: Gayatri Ravikumar, Shalini Mullick, Anuradha Ananthamurthy, Marjorie Correa
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:Case Reports in Surgery
Online Access:http://dx.doi.org/10.1155/2011/602853
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spelling doaj-7016a6782db74fa795c6f65d3a6737122020-11-24T23:05:04ZengHindawi LimitedCase Reports in Surgery2090-69002090-69192011-01-01201110.1155/2011/602853602853Primary Synovial Sarcoma of the Mediastinum : A Case ReportGayatri Ravikumar0Shalini Mullick1Anuradha Ananthamurthy2Marjorie Correa3Department of Pathology, St. John's Medical College, Sarjapur Road, Koramangala, Bangalore 560034, IndiaDepartment of Pathology, St. John's Medical College, Sarjapur Road, Koramangala, Bangalore 560034, IndiaDepartment of Pathology, St. John's Medical College, Sarjapur Road, Koramangala, Bangalore 560034, IndiaDepartment of Pathology, St. John's Medical College, Sarjapur Road, Koramangala, Bangalore 560034, IndiaSynovial sarcomas commonly occur in the extremities of young adults. A primary occurrence in the mediastinum is very rare with only a few reported cases in the world literature. This paper is about a 42-year-old male who presented with chest pain and dyspnoea on exertion. Imaging showed an anterior mediastinal mass with adhesions to the lung. Pathological examination of the resected mass showed a biphasic neoplasm with a spindle cell component admixed with gland-like elements. The tumour showed positive staining with cytokeratin, epithelial membrane antigen, and Bcl-2 confirming the diagnosis of a biphasic synovial sarcoma. A wide range of neoplasms, both primary and metastatic, occur in the mediastinum, which pose considerable diagnostic difficulties. A synovial sarcoma should always be considered in the differential diagnosis, and immunohistochemistry is an important adjuvant tool in this situation. This paper highlights the importance of recognizing an unusual presentation of this aggressive neoplasm to aid appropriate clinical management.http://dx.doi.org/10.1155/2011/602853
collection DOAJ
language English
format Article
sources DOAJ
author Gayatri Ravikumar
Shalini Mullick
Anuradha Ananthamurthy
Marjorie Correa
spellingShingle Gayatri Ravikumar
Shalini Mullick
Anuradha Ananthamurthy
Marjorie Correa
Primary Synovial Sarcoma of the Mediastinum : A Case Report
Case Reports in Surgery
author_facet Gayatri Ravikumar
Shalini Mullick
Anuradha Ananthamurthy
Marjorie Correa
author_sort Gayatri Ravikumar
title Primary Synovial Sarcoma of the Mediastinum : A Case Report
title_short Primary Synovial Sarcoma of the Mediastinum : A Case Report
title_full Primary Synovial Sarcoma of the Mediastinum : A Case Report
title_fullStr Primary Synovial Sarcoma of the Mediastinum : A Case Report
title_full_unstemmed Primary Synovial Sarcoma of the Mediastinum : A Case Report
title_sort primary synovial sarcoma of the mediastinum : a case report
publisher Hindawi Limited
series Case Reports in Surgery
issn 2090-6900
2090-6919
publishDate 2011-01-01
description Synovial sarcomas commonly occur in the extremities of young adults. A primary occurrence in the mediastinum is very rare with only a few reported cases in the world literature. This paper is about a 42-year-old male who presented with chest pain and dyspnoea on exertion. Imaging showed an anterior mediastinal mass with adhesions to the lung. Pathological examination of the resected mass showed a biphasic neoplasm with a spindle cell component admixed with gland-like elements. The tumour showed positive staining with cytokeratin, epithelial membrane antigen, and Bcl-2 confirming the diagnosis of a biphasic synovial sarcoma. A wide range of neoplasms, both primary and metastatic, occur in the mediastinum, which pose considerable diagnostic difficulties. A synovial sarcoma should always be considered in the differential diagnosis, and immunohistochemistry is an important adjuvant tool in this situation. This paper highlights the importance of recognizing an unusual presentation of this aggressive neoplasm to aid appropriate clinical management.
url http://dx.doi.org/10.1155/2011/602853
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