eISSN: 2084-9869
ISSN: 1233-9687
Polish Journal of Pathology
Current issue Archive Manuscripts accepted About the journal Supplements Editorial board Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
SCImago Journal & Country Rank
4/2013
vol. 64
 
Share:
Share:
more
 
 
abstract:

Bilateral papillary renal cell carcinoma and angiomyolipoma in the patients with autosomal dominant polycystic kidney disease: case report of two cases and literature review

Sachiko Konosu-Fukaya
,
Yasuhiro Nakamura
,
Fumiyoshi Fujishima
,
Atsuko Kasajima
,
Yayoi Takahashi
,
Kensuke Joh
,
Yoshihiro Ikeda
,
Naomasa Ioritani
,
Mika Watanabe
,
Hironobu Sasano

POL J PATHOL 2013; 64 (4): 303-307
Online publish date: 2013/12/26
View full text
Get citation
ENW
EndNote
BIB
JabRef, Mendeley
RIS
Papers, Reference Manager, RefWorks, Zotero
AMA
APA
Chicago
Harvard
MLA
Vancouver
 
PlumX metrics:
We herein report two rare cases of bilateral renal neoplasms associated with autosomal dominant polycystic kidney disease (ADPKD). Case 1: Bilateral nephrectomy was performed on bilateral renal masses in a 58-year-old man with ADPKD. Case 2: Bilateral nephrectomy was performed on bilateral renal masses in a 32-year-old man with clinically suspected ADPKD. In case 1, angiomyolipoma (AML) and papillary renal cell carcinoma (PRCC) (type 1) were detected in the bilateral kidneys. In case 2, PRCC (type 1) was detected in the bilateral kidneys.
keywords:

autosomal dominant polycystic kidney disease, papillary renal cell carcinoma, angiomyolipoma

Quick links
© 2022 Termedia Sp. z o.o. All rights reserved.
Developed by Bentus.