常染色体显性遗传性多囊肾病患者的双侧肾细胞癌
Bilateral renal cell carcinoma in a patient with autosomal dominant polycystic kidney disease.
作者信息
Chang Yu-Lung, Chung Hsiao-Jen, Chen Kuang-Kuo
机构信息
Division of Urology, Department of Surgery, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
出版信息
J Chin Med Assoc. 2007 Sep;70(9):403-5. doi: 10.1016/S1726-4901(08)70029-7.
Abstract
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.
摘要
常染色体显性多囊肾病（ADPKD）合并肾细胞癌（RCC）非常罕见。自1954年以来，仅报道了11例ADPKD合并双侧RCC的病例。在此，我们报告一例58岁男性患者，其因ADPKD合并双侧不同细胞类型的RCC以及终末期肾病在规律血液透析治疗下行腹腔镜双侧根治性肾切除术。
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