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Primary renal synovial sarcoma

Primary synovial sarcoma (SS) of kidney is very rare and difficult to diagnose. Here, we present a case of a 21-year-old female clinically diagnosed as renal cell carcinoma. Right nephrectomy specimen showed a cystic tumor in the upper pole of kidney with areas of hemorrhage and solid growth. Histol...

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Autores principales: Grampurohit, Vandana U., Myageri, Aneel, Rao, Ravikala V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130475/
https://www.ncbi.nlm.nih.gov/pubmed/21747606
http://dx.doi.org/10.4103/0974-7796.82182
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author Grampurohit, Vandana U.
Myageri, Aneel
Rao, Ravikala V.
author_facet Grampurohit, Vandana U.
Myageri, Aneel
Rao, Ravikala V.
author_sort Grampurohit, Vandana U.
collection PubMed
description Primary synovial sarcoma (SS) of kidney is very rare and difficult to diagnose. Here, we present a case of a 21-year-old female clinically diagnosed as renal cell carcinoma. Right nephrectomy specimen showed a cystic tumor in the upper pole of kidney with areas of hemorrhage and solid growth. Histologically, it showed poorly differentiated cells with hemangiopericytoma-like vascular pattern. Morphologic and immunohistochemical features were compatible with the diagnosis of poorly differentiated SS of kidney. Primary renal SS is a recently described entity. To the best of our knowledge, approximately 34 cases have been reported till date and this is the eighth documented case of poorly differentiated variant. Most of the time, poorly differentiated SS of kidney exhibits hemangiopericytoma like histology. Reverse transcriptase-polymerase chain reaction analysis to demonstrate SYT–SSX fusion gene transcript helps to confirm the diagnosis.
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spelling pubmed-31304752011-07-11 Primary renal synovial sarcoma Grampurohit, Vandana U. Myageri, Aneel Rao, Ravikala V. Urol Ann Case Report Primary synovial sarcoma (SS) of kidney is very rare and difficult to diagnose. Here, we present a case of a 21-year-old female clinically diagnosed as renal cell carcinoma. Right nephrectomy specimen showed a cystic tumor in the upper pole of kidney with areas of hemorrhage and solid growth. Histologically, it showed poorly differentiated cells with hemangiopericytoma-like vascular pattern. Morphologic and immunohistochemical features were compatible with the diagnosis of poorly differentiated SS of kidney. Primary renal SS is a recently described entity. To the best of our knowledge, approximately 34 cases have been reported till date and this is the eighth documented case of poorly differentiated variant. Most of the time, poorly differentiated SS of kidney exhibits hemangiopericytoma like histology. Reverse transcriptase-polymerase chain reaction analysis to demonstrate SYT–SSX fusion gene transcript helps to confirm the diagnosis. Medknow Publications 2011 /pmc/articles/PMC3130475/ /pubmed/21747606 http://dx.doi.org/10.4103/0974-7796.82182 Text en Copyright: © Urology Annals 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
Grampurohit, Vandana U.
Myageri, Aneel
Rao, Ravikala V.
Primary renal synovial sarcoma
title Primary renal synovial sarcoma
title_full Primary renal synovial sarcoma
title_fullStr Primary renal synovial sarcoma
title_full_unstemmed Primary renal synovial sarcoma
title_short Primary renal synovial sarcoma
title_sort primary renal synovial sarcoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130475/
https://www.ncbi.nlm.nih.gov/pubmed/21747606
http://dx.doi.org/10.4103/0974-7796.82182
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