Department of Urology, The Catholic University of Korea Daejeon St, Mary's Hospital, Daeheung-dong, Jung-gu, Daejeon, 301-723, Korea.
World J Surg Oncol. 2013 Aug 8;11(1):181. doi: 10.1186/1477-7819-11-181.
Extrapulmonary small cell carcinomas have been reported in a variety of organs, and their incidence in the genitourinary tract is second only to that in the gastrointestinal tract. To date, however, only a few cases of small cell carcinoma of the ureter have been reported. Because the extreme rarity of this type of carcinoma, its clinical behaviour, diagnostic methods, and effective treatment modalities have not yet been determined.
A 59-year-old man presented with a 1-month history of painless gross haematuria. Urine cytopathology revealed a urothelial carcinoma and computed tomography revealed left hydronephroureterosis with a distal ureteral stone and a mildly enhanced fungating mass just below the stone-impacted site. The preoperative TNM stage was T2N0M0. The patient underwent simultaneous diagnostic ureterorenoscopy and left laparoscopic nephroureterectomy with bladder cuff resection. Gross examination showed a 3.5 × 3.0 × 0.8 cm white, partly yellow mass in the left distal ureter. Light microscopy showed a small cell carcinoma, overlaid on a urothelial carcinoma in situ, invading the ureter and external lateral resection margins. The small cell carcinoma was diffusely positive for neuron-specific enolase, and exhibited focal positivity for CD 56, synaptophysin, chromogranin and cytokeratin 20. The patient was treated with adjuvant chemotherapy, consisting of cisplatin and etoposide, and radiation therapy, and has been well, without evidence of tumour recurrence or metastasis in the 10 months after surgery.
Small cell carcinoma of the ureter is rare. Although its clinical behaviour and diagnostic modalities have not been determined and it has yet to be diagnosed immunohistopathologically, multimodality treatment including surgery, chemotherapy and radiotherapy may improve patient survival.
肺外小细胞癌已在多种器官中被报道,其在泌尿生殖道的发生率仅次于胃肠道。然而,迄今为止,仅有少数输尿管小细胞癌病例被报道。由于这种类型的癌极其罕见,其临床行为、诊断方法和有效的治疗方式尚未确定。
一名 59 岁男性因无痛性肉眼血尿病史 1 个月就诊。尿液细胞学检查显示为尿路上皮癌,计算机断层扫描显示左侧肾盂输尿管积水,伴有远端输尿管结石和结石部位下方轻度增强的蕈样肿块。术前 TNM 分期为 T2N0M0。患者接受了同期诊断性输尿管镜检查和左侧腹腔镜肾输尿管切除术,同时切除膀胱袖套。大体检查显示左侧远端输尿管有一个 3.5×3.0×0.8cm 的白色、部分黄色肿块。光镜下显示为小细胞癌,覆盖在上皮原位癌上,侵犯输尿管和外部侧切除边缘。小细胞癌弥漫性神经元特异性烯醇化酶阳性,局灶性 CD56、突触素、嗜铬粒蛋白和细胞角蛋白 20 阳性。患者接受了顺铂和依托泊苷辅助化疗和放疗,术后 10 个月,患者情况良好,无肿瘤复发或转移的迹象。
输尿管小细胞癌罕见。尽管其临床行为和诊断方式尚未确定,并且尚未通过免疫组织化学病理检查确诊,但包括手术、化疗和放疗在内的多模态治疗可能会改善患者的生存。