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Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature

Translocation renal cell carcinoma (RCC) is a family of rare tumors recently identified in the pediatric and young adult population. We report the first case of a young woman from French West Indies with sickle cell anemia who developed a translocation RCC t(6;11)(p21;q12). Usually people with the s...

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Autores principales: Chaste, Damien, Vian, Emmanuel, Verhoest, Gregory, Blanchet, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Urological Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935073/
https://www.ncbi.nlm.nih.gov/pubmed/24578813
http://dx.doi.org/10.4111/kju.2014.55.2.145
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author Chaste, Damien
Vian, Emmanuel
Verhoest, Gregory
Blanchet, Pascal
author_facet Chaste, Damien
Vian, Emmanuel
Verhoest, Gregory
Blanchet, Pascal
author_sort Chaste, Damien
collection PubMed
description Translocation renal cell carcinoma (RCC) is a family of rare tumors recently identified in the pediatric and young adult population. We report the first case of a young woman from French West Indies with sickle cell anemia who developed a translocation RCC t(6;11)(p21;q12). Usually people with the sickle cell condition are known to develop renal medullary carcinoma (RMC). To our knowledge, this is the first case described in the literature of a translocation RCC associated with sickle cell disease. Here we discuss the relation between translocation RCC, RMC, and sickle cell disease.
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spelling pubmed-39350732014-02-27 Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature Chaste, Damien Vian, Emmanuel Verhoest, Gregory Blanchet, Pascal Korean J Urol Case Report Translocation renal cell carcinoma (RCC) is a family of rare tumors recently identified in the pediatric and young adult population. We report the first case of a young woman from French West Indies with sickle cell anemia who developed a translocation RCC t(6;11)(p21;q12). Usually people with the sickle cell condition are known to develop renal medullary carcinoma (RMC). To our knowledge, this is the first case described in the literature of a translocation RCC associated with sickle cell disease. Here we discuss the relation between translocation RCC, RMC, and sickle cell disease. The Korean Urological Association 2014-02 2014-02-14 /pmc/articles/PMC3935073/ /pubmed/24578813 http://dx.doi.org/10.4111/kju.2014.55.2.145 Text en © The Korean Urological Association, 2014 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
Chaste, Damien
Vian, Emmanuel
Verhoest, Gregory
Blanchet, Pascal
Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature
title Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature
title_full Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature
title_fullStr Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature
title_full_unstemmed Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature
title_short Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature
title_sort translocation renal cell carcinoma t(6;11)(p21;q12) and sickle cell anemia: first report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935073/
https://www.ncbi.nlm.nih.gov/pubmed/24578813
http://dx.doi.org/10.4111/kju.2014.55.2.145
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