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Synovial Sarcoma of the Thyroid Gland

Primary synovial sarcoma of the thyroid is an extremely rare condition which has only been reported twice in the literature. We herein report a case of highly aggressive and rapidly lethal primary synovial sarcoma of the thyroid. A 72-year-old woman presented with extensive local invasion, rapid pro...

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Autores principales: Ryu, Chang Hwan, Cho, Kyung-Ja, Choi, Seung-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Otorhinolaryngology-Head and Neck Surgery 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250586/
https://www.ncbi.nlm.nih.gov/pubmed/22232717
http://dx.doi.org/10.3342/ceo.2011.4.4.204
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author Ryu, Chang Hwan
Cho, Kyung-Ja
Choi, Seung-Ho
author_facet Ryu, Chang Hwan
Cho, Kyung-Ja
Choi, Seung-Ho
author_sort Ryu, Chang Hwan
collection PubMed
description Primary synovial sarcoma of the thyroid is an extremely rare condition which has only been reported twice in the literature. We herein report a case of highly aggressive and rapidly lethal primary synovial sarcoma of the thyroid. A 72-year-old woman presented with extensive local invasion, rapid progression, and early distant metastasis secondary to primary thyroid synovial sarcoma. The tumor exhibited an atypical histologic and immunohistochemical staining pattern. Detection of SYT/SSX fusion transcript confirmed the diagnosis of synovial sarcoma. Due to the aggressive nature of primary synovial sarcoma of the thyroid gland, early diagnosis and comprehensive treatment including wide resection and postoperative chemoradiation is required.
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spelling pubmed-32505862012-01-09 Synovial Sarcoma of the Thyroid Gland Ryu, Chang Hwan Cho, Kyung-Ja Choi, Seung-Ho Clin Exp Otorhinolaryngol Case Report Primary synovial sarcoma of the thyroid is an extremely rare condition which has only been reported twice in the literature. We herein report a case of highly aggressive and rapidly lethal primary synovial sarcoma of the thyroid. A 72-year-old woman presented with extensive local invasion, rapid progression, and early distant metastasis secondary to primary thyroid synovial sarcoma. The tumor exhibited an atypical histologic and immunohistochemical staining pattern. Detection of SYT/SSX fusion transcript confirmed the diagnosis of synovial sarcoma. Due to the aggressive nature of primary synovial sarcoma of the thyroid gland, early diagnosis and comprehensive treatment including wide resection and postoperative chemoradiation is required. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2011-12 2011-02-07 /pmc/articles/PMC3250586/ /pubmed/22232717 http://dx.doi.org/10.3342/ceo.2011.4.4.204 Text en Copyright © 2011 by Korean Society of Otorhinolaryngology-Head and Neck Surgery. http://creativecommons.org/licenses/by-nc/3.0 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
Ryu, Chang Hwan
Cho, Kyung-Ja
Choi, Seung-Ho
Synovial Sarcoma of the Thyroid Gland
title Synovial Sarcoma of the Thyroid Gland
title_full Synovial Sarcoma of the Thyroid Gland
title_fullStr Synovial Sarcoma of the Thyroid Gland
title_full_unstemmed Synovial Sarcoma of the Thyroid Gland
title_short Synovial Sarcoma of the Thyroid Gland
title_sort synovial sarcoma of the thyroid gland
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250586/
https://www.ncbi.nlm.nih.gov/pubmed/22232717
http://dx.doi.org/10.3342/ceo.2011.4.4.204
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