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Multifocal Renal Cell Carcinoma of Different Histological Subtypes in Autosomal Dominant Polycystic Kidney Disease
Korean Journal of Pathology ; : 382-386, 2012.
Article in English | WPRIM | ID: wpr-32984
ABSTRACT
Renal cell carcinoma (RCC) in autosomal dominant polycystic kidney (ADPKD) is rare. To date, 54 cases of RCC in ADPKD have been reported. Among these, only 2 cases have different histologic types of RCC. Here we describe a 45-year-old man who received radical nephrectomy for multifocal RCC with synchronous papillary and clear cell histology in ADPKD and chronic renal failure under regular hemodialysis. The case reported herein is another example of the rare pathological finding of RCC arising in a patient with ADPKD.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Carcinoma, Renal Cell / Renal Dialysis / Polycystic Kidney, Autosomal Dominant / Kidney Failure, Chronic / Nephrectomy Limits: Humans Language: English Journal: Korean Journal of Pathology Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Carcinoma, Renal Cell / Renal Dialysis / Polycystic Kidney, Autosomal Dominant / Kidney Failure, Chronic / Nephrectomy Limits: Humans Language: English Journal: Korean Journal of Pathology Year: 2012 Type: Article