Miwa S, Fuse H, Hirano S, Masuda S
Department of Urology, Kouseiren Takaoka Hospital, Takaoka, Japan.
Int J Urol. 2001 Oct;8(10):572-4. doi: 10.1046/j.1442-2042.2001.00372.x.
We present a case of renal pelvic transitional cell carcinoma (TCC) accompanied by autosomal dominant polycystic kidney disease (ADPKD). An 81-year-old woman on long-term hemodialysis for ADPKD visited the Department of Urology at Kouseiren Takaoko Hospital, complaining of asymptomatic macroscopic hematuria. Retrograde pyelogram showed an irregular filling defect in the right renal pelvis, which suggested the right renal pelvic tumor. We performed right nephrectomy and transurethral removal of the right ureter. Histological diagnosis demonstrated renal pelvic TCC.
我们报告一例伴有常染色体显性遗传性多囊肾病(ADPKD)的肾盂移行细胞癌(TCC)。一名因ADPKD接受长期血液透析的81岁女性前往高岗厚生连医院泌尿外科就诊,主诉无症状肉眼血尿。逆行肾盂造影显示右肾盂有不规则充盈缺损,提示右肾盂肿瘤。我们进行了右肾切除术及经尿道右输尿管切除术。组织学诊断为肾盂移行细胞癌。