A rare case of bilateral sequential spermatocytic seminoma

Spermatocytic seminoma (SS) is a rare testicular neoplasm characterized by a palpable, painless, slowly enlarging mass in the testis. Even more rare is a synchronous bilateral presentation. Only eight cases of bilateral SS have been reported in the literature, of which three cases were present with...

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Detalles Bibliográficos
Autores principales: Xu, Ning, Li, Fubiao, Tian, Runhui, Shao, Mingming, Liu, Lingyun, Guo, Kaimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751534/
https://www.ncbi.nlm.nih.gov/pubmed/23915031
http://dx.doi.org/10.1186/1477-7819-11-175
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author Xu, Ning
Li, Fubiao
Tian, Runhui
Shao, Mingming
Liu, Lingyun
Guo, Kaimin
author_facet Xu, Ning
Li, Fubiao
Tian, Runhui
Shao, Mingming
Liu, Lingyun
Guo, Kaimin
author_sort Xu, Ning
collection PubMed
description Spermatocytic seminoma (SS) is a rare testicular neoplasm characterized by a palpable, painless, slowly enlarging mass in the testis. Even more rare is a synchronous bilateral presentation. Only eight cases of bilateral SS have been reported in the literature, of which three cases were present with synchronous testis enlargement, and five were sequential. Here, we report an additional case of synchronous bilateral SS and present a comprehensive relevant literature review concerning clinical features, histopathology, and treatment.
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spelling pubmed-37515342013-08-24 A rare case of bilateral sequential spermatocytic seminoma Xu, Ning Li, Fubiao Tian, Runhui Shao, Mingming Liu, Lingyun Guo, Kaimin World J Surg Oncol Case Report Spermatocytic seminoma (SS) is a rare testicular neoplasm characterized by a palpable, painless, slowly enlarging mass in the testis. Even more rare is a synchronous bilateral presentation. Only eight cases of bilateral SS have been reported in the literature, of which three cases were present with synchronous testis enlargement, and five were sequential. Here, we report an additional case of synchronous bilateral SS and present a comprehensive relevant literature review concerning clinical features, histopathology, and treatment. BioMed Central 2013-08-06 /pmc/articles/PMC3751534/ /pubmed/23915031 http://dx.doi.org/10.1186/1477-7819-11-175 Text en Copyright ©2013 Xu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Xu, Ning
Li, Fubiao
Tian, Runhui
Shao, Mingming
Liu, Lingyun
Guo, Kaimin
A rare case of bilateral sequential spermatocytic seminoma
title A rare case of bilateral sequential spermatocytic seminoma
title_full A rare case of bilateral sequential spermatocytic seminoma
title_fullStr A rare case of bilateral sequential spermatocytic seminoma
title_full_unstemmed A rare case of bilateral sequential spermatocytic seminoma
title_short A rare case of bilateral sequential spermatocytic seminoma
title_sort rare case of bilateral sequential spermatocytic seminoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751534/
https://www.ncbi.nlm.nih.gov/pubmed/23915031
http://dx.doi.org/10.1186/1477-7819-11-175
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