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Multifocal Renal Cell Carcinoma of Different Histological Subtypes in Autosomal Dominant Polycystic Kidney Disease

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³ª±â¿ë, ±èÇö¼ö, ¹Ú¿ë±¸, À强±¸, ±èÀ±È­,
¼Ò¼Ó »ó¼¼Á¤º¸
³ª±â¿ë ( Na Ki-Yong ) 
Kyung Hee University School of Medicine Department of Pathology

±èÇö¼ö ( Kim Hyun-Soo ) 
Kyung Hee University School of Medicine Department of Pathology
¹Ú¿ë±¸ ( Park Yong-Koo ) 
Kyung Hee University School of Medicine Department of Pathology
À强±¸ ( Chang Sung-Goo ) 
Kyung Hee University School of Medicine Department of Urology
±èÀ±È­ ( Kim Youn-Wha ) 
Kyung Hee University School of Medicine Department of Pathology

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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Polycystic kidney; autosomal dominant; Carcinoma; renal cell; Clear cell; Papillary

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