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Case of hereditary papillary renal cell carcinoma

Renal cell carcinoma is the most common type of renal malignancy and it originates from the renal tubular epithelium. Due to the diversity in the histopathological and molecular characteristics, it is typically subclassified into five different categories. Papillary renal cell carcinoma is one subcl...

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Detalles Bibliográficos
Autores principales: Mustafa, Sadaf, Jadidi, Nima, Faraj, Sheila F., Rodriguez, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714050/
https://www.ncbi.nlm.nih.gov/pubmed/23882344
http://dx.doi.org/10.3402/jchimp.v1i4.9468
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author Mustafa, Sadaf
Jadidi, Nima
Faraj, Sheila F.
Rodriguez, Ronald
author_facet Mustafa, Sadaf
Jadidi, Nima
Faraj, Sheila F.
Rodriguez, Ronald
author_sort Mustafa, Sadaf
collection PubMed
description Renal cell carcinoma is the most common type of renal malignancy and it originates from the renal tubular epithelium. Due to the diversity in the histopathological and molecular characteristics, it is typically subclassified into five different categories. Papillary renal cell carcinoma is one subclassification and it includes two variants: sporadic and hereditary. Although the hereditary form comprises a smaller number of cases of papillary renal cell carcinoma, an understanding of the molecular pathways and genetic changes continues to play a significant role in the development of new targeted therapies. Along with recommending appropriate lifestyle modification, further investigation into the molecular pathogenesis of hereditary papillary renal cell carcinoma will continue to be invaluable for the clinical management of renal cell carcinoma. In this article, we discuss a case of the hereditary papillary renal cell carcinoma along with an overview of the disease.
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spelling pubmed-37140502013-07-23 Case of hereditary papillary renal cell carcinoma Mustafa, Sadaf Jadidi, Nima Faraj, Sheila F. Rodriguez, Ronald J Community Hosp Intern Med Perspect Case Report Renal cell carcinoma is the most common type of renal malignancy and it originates from the renal tubular epithelium. Due to the diversity in the histopathological and molecular characteristics, it is typically subclassified into five different categories. Papillary renal cell carcinoma is one subclassification and it includes two variants: sporadic and hereditary. Although the hereditary form comprises a smaller number of cases of papillary renal cell carcinoma, an understanding of the molecular pathways and genetic changes continues to play a significant role in the development of new targeted therapies. Along with recommending appropriate lifestyle modification, further investigation into the molecular pathogenesis of hereditary papillary renal cell carcinoma will continue to be invaluable for the clinical management of renal cell carcinoma. In this article, we discuss a case of the hereditary papillary renal cell carcinoma along with an overview of the disease. Co-Action Publishing 2012-01-26 /pmc/articles/PMC3714050/ /pubmed/23882344 http://dx.doi.org/10.3402/jchimp.v1i4.9468 Text en © 2011 Sadaf Mustafa et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mustafa, Sadaf
Jadidi, Nima
Faraj, Sheila F.
Rodriguez, Ronald
Case of hereditary papillary renal cell carcinoma
title Case of hereditary papillary renal cell carcinoma
title_full Case of hereditary papillary renal cell carcinoma
title_fullStr Case of hereditary papillary renal cell carcinoma
title_full_unstemmed Case of hereditary papillary renal cell carcinoma
title_short Case of hereditary papillary renal cell carcinoma
title_sort case of hereditary papillary renal cell carcinoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714050/
https://www.ncbi.nlm.nih.gov/pubmed/23882344
http://dx.doi.org/10.3402/jchimp.v1i4.9468
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