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Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype

BACKGROUND: XP11.2 renal translocation carcinomas are often encountered in paediatric group of patients where they are believed to be rather indolent. They are rare but more aggressive in young adults. They are slow growing, sometimes without characteristic symptoms and their biologic behaviour is u...

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Autores principales: Kmetec, Andrej, Jeruc, Jera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita, Warsaw 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078039/
https://www.ncbi.nlm.nih.gov/pubmed/24991210
http://dx.doi.org/10.2478/raon-2013-0077
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author Kmetec, Andrej
Jeruc, Jera
author_facet Kmetec, Andrej
Jeruc, Jera
author_sort Kmetec, Andrej
collection PubMed
description BACKGROUND: XP11.2 renal translocation carcinomas are often encountered in paediatric group of patients where they are believed to be rather indolent. They are rare but more aggressive in young adults. They are slow growing, sometimes without characteristic symptoms and their biologic behaviour is uncertain. CASE REPORT: We report two cases of this type of tumour in Slovenian young adult males with long and unusual history. Tumours were confirmed imunohistologically by positive reaction for CD10, P504S and TFE3. CONCLUSIONS: According to the indications in the literature prognosis of these tumours in young adults depends upon the stage. It seems that cysts, haematomas and necrosis around the kidney are often encountered in these tumours. In advanced stage with lymph nodes involvement or distant metastases, the prognosis is poor. Surgery seems to be basic mode of therapy.
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spelling pubmed-40780392014-07-02 Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype Kmetec, Andrej Jeruc, Jera Radiol Oncol Case Report BACKGROUND: XP11.2 renal translocation carcinomas are often encountered in paediatric group of patients where they are believed to be rather indolent. They are rare but more aggressive in young adults. They are slow growing, sometimes without characteristic symptoms and their biologic behaviour is uncertain. CASE REPORT: We report two cases of this type of tumour in Slovenian young adult males with long and unusual history. Tumours were confirmed imunohistologically by positive reaction for CD10, P504S and TFE3. CONCLUSIONS: According to the indications in the literature prognosis of these tumours in young adults depends upon the stage. It seems that cysts, haematomas and necrosis around the kidney are often encountered in these tumours. In advanced stage with lymph nodes involvement or distant metastases, the prognosis is poor. Surgery seems to be basic mode of therapy. Versita, Warsaw 2014-04-25 /pmc/articles/PMC4078039/ /pubmed/24991210 http://dx.doi.org/10.2478/raon-2013-0077 Text en Copyright © by Association of Radiology & Oncology http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Case Report
Kmetec, Andrej
Jeruc, Jera
Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
title Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
title_full Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
title_fullStr Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
title_full_unstemmed Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
title_short Xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
title_sort xp 11.2 translocation renal carcinoma in young adults; recently classified distinct subtype
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078039/
https://www.ncbi.nlm.nih.gov/pubmed/24991210
http://dx.doi.org/10.2478/raon-2013-0077
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