Tsuzuki M, Tochimoto M, Tsujino S, Akiyama A, Aizawa T, Ohno Y, Yamamoto S, Noda K, Miki M
Department of Urology, Tokyo Medical College.
Hinyokika Kiyo. 1995 Sep;41(9):679-82.
A 42-year-old man diagnosed with von Willebrand disease 7 years earlier visited his home doctor with a chief complaint of gross hematuria. Abdominal ultrasonography showed bilateral renal tumors. He was referred to our hospital on June 15, 1993. His mother also had von Hippel-Lindau disease and was treated by hemodialysis after bilateral nephrectomy. The examination and imaging revealed bilateral renal cell carcinoma of von Hippel-Lindau disease associated with von Willebrand disease. Partial nephrectomy and enucleation for a small tumor on the right side and enucleations for five tumors on the left side were performed. Histological diagnosis of all tumors were renal cell carcinoma, clear cell subtype, grade 1 approximately 2. The patient has been well without local recurrence or distant metastasis for 16 months since the operation. This is the first case of bilateral renal cell carcinoma of von Hippel-Lindau disease associated with von Willebrand disease in Japan.
一名7年前被诊断为血管性血友病的42岁男性因肉眼血尿为主诉前往家庭医生处就诊。腹部超声显示双侧肾肿瘤。1993年6月15日他被转诊至我院。他的母亲也患有希佩尔-林道病,双侧肾切除术后接受血液透析治疗。检查和影像学检查显示血管性血友病合并希佩尔-林道病的双侧肾细胞癌。对右侧一个小肿瘤进行了部分肾切除术和剜除术,对左侧五个肿瘤进行了剜除术。所有肿瘤的组织学诊断均为肾细胞癌,透明细胞亚型,1级,约2级。自手术以来,患者已健康存活16个月,无局部复发或远处转移。这是日本首例血管性血友病合并希佩尔-林道病的双侧肾细胞癌病例。