Fukushima Hiroshi, Koga Fumitaka, Tatokoro Manabu, Yokoyama Minato, Saito Kazutaka, Masuda Hitoshi, Fujii Yasuhisa, Kawakami Satoru, Kihara Kazunori
Department of Urology, Tokyo Medical and Dental University, Graduate School, Tokyo, Japan.
Nihon Hinyokika Gakkai Zasshi. 2011 Jul;102(4):638-43. doi: 10.5980/jpnjurol.102.638.
Primary small cell carcinoma of the renal pelvis is a rare and aggressive disease; reportedly, a mean survival is only 8 months. A 78 year-old woman with chronic kidney disease was referred to our hospital complaining of asymptomatic gross hematoturia. On imaging studies and voided urine cytology, diagnosis of right renal pelvic cancer (cT2N0M0) was made. She underwent total nephroureterectomy. Pathological diagnosis was small cell carcinoma, infiltrating into the renal parenchyma, with lymphovascular invasion. Post-operatively, hemodialysis was introduced. Five months after the operation, new lesions developed in the right adrenal gland, aortocaval lymph nodes and subcutaneous layer of the right back. The subcutaneous mass was surgically removed and low-dose chemoradiotherapy (sigma 45 Gy/25 Fr/32 d + cisplatin 10 mg/d for 2 d x 2) was given to the other lesions. Although the lesions regressed to CR, new small masses emerged in the muscle layers of the right flank 14 months after total nephroureterectomy. Low-dose chemoradiotherapy (sigma 40 Gy/20 Fr/29 d + cisplatin 10 mg/d for 2 d x 2) to these lesions successfully brought CR. She is alive without any evidence of disease at 3 years after total nephroureterectomy.
肾盂原发性小细胞癌是一种罕见且侵袭性强的疾病;据报道,平均生存期仅8个月。一名患有慢性肾脏病的78岁女性因无症状肉眼血尿被转诊至我院。经影像学检查和尿脱落细胞学检查,诊断为右肾盂癌(cT2N0M0)。她接受了全肾输尿管切除术。病理诊断为小细胞癌,侵犯肾实质,伴脉管侵犯。术后开始进行血液透析。术后5个月,右肾上腺、主动脉腔静脉淋巴结及右背部皮下层出现新病灶。对皮下肿块进行了手术切除,并对其他病灶给予低剂量放化疗(45 Gy/25次/32天 + 顺铂10 mg/天,共2天,重复2次)。尽管病灶消退至完全缓解,但在全肾输尿管切除术后14个月,右腰大肌层出现新的小肿块。对这些病灶给予低剂量放化疗(40 Gy/20次/29天 + 顺铂10 mg/天,共2天,重复2次)成功使其达到完全缓解。全肾输尿管切除术后3年,她仍存活,无疾病证据。