Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas

Clear cell papillary renal cell carcinoma (CCPRCC) is a newly recognized entity in the 2016 WHO classification and usually presents as a small, circumscribed, solitary mass of indolent nature. CCPRCCs could seldom occur in conjunction with other synchronous or metachronous kidney tumors and even les...

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Main Authors: Daniel A. Anderson, Maria S. Tretiakova
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Case Reports in Pathology
Online Access:http://dx.doi.org/10.1155/2017/9672368
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author Daniel A. Anderson
Maria S. Tretiakova
author_facet Daniel A. Anderson
Maria S. Tretiakova
author_sort Daniel A. Anderson
collection DOAJ
description Clear cell papillary renal cell carcinoma (CCPRCC) is a newly recognized entity in the 2016 WHO classification and usually presents as a small, circumscribed, solitary mass of indolent nature. CCPRCCs could seldom occur in conjunction with other synchronous or metachronous kidney tumors and even less frequently as bilateral masses. To our knowledge, multiple bilateral CCPRCCs have never been described with the existence of a synchronous well-differentiated neuroendocrine tumor of the kidney and hence reported here as a unique case. This case report highlights the importance in considering this entity and its unusual presentation in the differential diagnosis as a possible mimicker of Von Hippel-Lindau syndrome.
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spelling doaj-art-db1ca3d21c8f4c86b382882ada7834282025-02-03T07:25:08ZengWileyCase Reports in Pathology2090-67812090-679X2017-01-01201710.1155/2017/96723689672368Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell CarcinomasDaniel A. Anderson0Maria S. Tretiakova1Department of Pathology, UWMC Anatomic Pathology, University of Washington, 1959 NE Pacific St., P.O. Box 356100, Seattle, WA 98195-6100, USADepartment of Pathology, University of Washington, 325 Ninth Avenue, P.O. Box 359791, Seattle, WA 98104, USAClear cell papillary renal cell carcinoma (CCPRCC) is a newly recognized entity in the 2016 WHO classification and usually presents as a small, circumscribed, solitary mass of indolent nature. CCPRCCs could seldom occur in conjunction with other synchronous or metachronous kidney tumors and even less frequently as bilateral masses. To our knowledge, multiple bilateral CCPRCCs have never been described with the existence of a synchronous well-differentiated neuroendocrine tumor of the kidney and hence reported here as a unique case. This case report highlights the importance in considering this entity and its unusual presentation in the differential diagnosis as a possible mimicker of Von Hippel-Lindau syndrome.http://dx.doi.org/10.1155/2017/9672368
spellingShingle Daniel A. Anderson
Maria S. Tretiakova
Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas
Case Reports in Pathology
title Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas
title_full Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas
title_fullStr Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas
title_full_unstemmed Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas
title_short Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas
title_sort primary renal carcinoid with bilateral multiple clear cell papillary renal cell carcinomas
url http://dx.doi.org/10.1155/2017/9672368
work_keys_str_mv AT danielaanderson primaryrenalcarcinoidwithbilateralmultipleclearcellpapillaryrenalcellcarcinomas
AT mariastretiakova primaryrenalcarcinoidwithbilateralmultipleclearcellpapillaryrenalcellcarcinomas