Bilateral Renal Cell Carcinoma in a Patient with Autosomal Dominant Polycystic Kidney Disease

Renal cell carcinoma (RCC) in autosomal dominant polycystic kidney disease (ADPKD) is very rare. Only 11 cases of bilateral RCC in ADPKD have been reported since 1954. Herein, we present a 58-year-old male who received laparoscopic bilateral radical nephrectomy for bilateral RCC with different cell...

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Bibliographic Details
Published inJournal of the Chinese Medical Association Vol. 70; no. 9; pp. 403 - 405
Main Authors Chang, Yu-Lung, Chung, Hsiao-Jen, Chen, Kuang-Kuo
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.09.2007
Subjects
autosomal dominant polycystic kidney disease
Carcinoma, Renal Cell - diagnosis
Carcinoma, Renal Cell - etiology
Carcinoma, Renal Cell - surgery
conventional renal cell carcinoma
Humans
Internal Medicine
Kidney Neoplasms - diagnosis
Kidney Neoplasms - etiology
Kidney Neoplasms - surgery
Male
Middle Aged
papillary renal cell carcinoma
Polycystic Kidney, Autosomal Dominant - complications
conventional renal cell carcinoma
papillary renal cell carcinoma
autosomal dominant polycystic kidney disease
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Summary:Renal cell carcinoma (RCC) in autosomal dominant polycystic kidney disease (ADPKD) is very rare. Only 11 cases of bilateral RCC in ADPKD have been reported since 1954. Herein, we present a 58-year-old male who received laparoscopic bilateral radical nephrectomy for bilateral RCC with different cell variants in ADPKD and end-stage renal disease under regular hemodialysis.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
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ObjectType-Report-1
ObjectType-Article-3
ISSN:1726-4901
1728-7731
DOI:10.1016/S1726-4901(08)70029-7