常染色体显性多囊肾病引起的肾细胞癌

Annals of Tropical Pathology Pub Date : 2021-01-01 DOI:10.4103/atp.atp_54_20

Muzammil Abdullahi, A. Ismail, Abdullahi Ahmad

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引用次数: 0

摘要

肾细胞癌(RCC)引起的常染色体显性多囊肾病(ADPKD)是罕见的。由于非特异性症状，在ADPKD患者中检测这种并发症是困难的。在这里，我们描述了一个年轻女性在ADPKD的背景下出现RCC的病例。她接受了根治性肾切除术，随后进行了辅助化疗。

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Renal cell carcinoma arising within autosomal dominant polycystic kidney disease

Renal cell carcinoma (RCC) arising within autosomal dominant polycystic kidney disease (ADPKD) is rare. The detection of this complication in patients with ADPKD is difficult owing to the nonspecific symptoms. Here, we describe a case of a young woman who presented with RCC in the background of ADPKD. She had radical nephrectomy, followed by adjuvant chemotherapy.

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Annals of Tropical Pathology

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