A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature

Primary renal mucinous cystadenocarcinoma is a very rare lesion of kidney which originates from the metaplasia of the renal pelvic uroepithelium. Only one case with primary mucinous cystadenocarcinoma has been reported in the English literature. We report second case of mucinous cystadenocarcinoma w...

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Autores principales: Tepeler, Abdulkadir, Erdem, Mehmet Remzi, Kurt, Omer, Topaktas, Ramazan, Kilicaslan, Isin, Armağan, Abdullah, Önol, Şinasi Yavuz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205935/
https://www.ncbi.nlm.nih.gov/pubmed/22110514
http://dx.doi.org/10.1155/2011/686283
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author Tepeler, Abdulkadir
Erdem, Mehmet Remzi
Kurt, Omer
Topaktas, Ramazan
Kilicaslan, Isin
Armağan, Abdullah
Önol, Şinasi Yavuz
author_facet Tepeler, Abdulkadir
Erdem, Mehmet Remzi
Kurt, Omer
Topaktas, Ramazan
Kilicaslan, Isin
Armağan, Abdullah
Önol, Şinasi Yavuz
author_sort Tepeler, Abdulkadir
collection PubMed
description Primary renal mucinous cystadenocarcinoma is a very rare lesion of kidney which originates from the metaplasia of the renal pelvic uroepithelium. Only one case with primary mucinous cystadenocarcinoma has been reported in the English literature. We report second case of mucinous cystadenocarcinoma which was radiologically classified as type-IIF Bosniak cyst in peripheral localization. We aimed to present this extreme and unusual entity with its radiological, surgical, and pathologic aspects under the light of literature.
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spelling pubmed-32059352011-11-22 A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature Tepeler, Abdulkadir Erdem, Mehmet Remzi Kurt, Omer Topaktas, Ramazan Kilicaslan, Isin Armağan, Abdullah Önol, Şinasi Yavuz Case Rep Med Case Report Primary renal mucinous cystadenocarcinoma is a very rare lesion of kidney which originates from the metaplasia of the renal pelvic uroepithelium. Only one case with primary mucinous cystadenocarcinoma has been reported in the English literature. We report second case of mucinous cystadenocarcinoma which was radiologically classified as type-IIF Bosniak cyst in peripheral localization. We aimed to present this extreme and unusual entity with its radiological, surgical, and pathologic aspects under the light of literature. Hindawi Publishing Corporation 2011 2011-10-29 /pmc/articles/PMC3205935/ /pubmed/22110514 http://dx.doi.org/10.1155/2011/686283 Text en Copyright © 2011 Abdulkadir Tepeler et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under 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
Tepeler, Abdulkadir
Erdem, Mehmet Remzi
Kurt, Omer
Topaktas, Ramazan
Kilicaslan, Isin
Armağan, Abdullah
Önol, Şinasi Yavuz
A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature
title A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature
title_full A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature
title_fullStr A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature
title_full_unstemmed A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature
title_short A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature
title_sort rare renal epithelial tumor: mucinous cystadenocarcinoma case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205935/
https://www.ncbi.nlm.nih.gov/pubmed/22110514
http://dx.doi.org/10.1155/2011/686283
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