Sood Akshay, Williamson Sean R, Leavitt David A
Vattikuti Urology Institute , Henry Ford Health System, Detroit, Michigan.
Department of Pathology, Henry Ford Health System , Detroit, Michigan.
J Endourol Case Rep. 2016 Nov 1;2(1):204-208. doi: 10.1089/cren.2016.0103. eCollection 2016.
Primary neuroendocrine tumors of the upper urinary tract are extremely rare. We report a case of small cell carcinoma of the ureter that presented masquerading as a distal ureteral stone. A 55-year-old lady presented to our clinic with 1 month history of right lower back pain and hematuria. Her history was notable for stage 1B mixed clear cell-endometroid cancer of the uterus status post radical abdominal hysterectomy with adjuvant radiotherapy, 7 years before the current episode. The patient had no evidence of recurrence. Initial noncontrast imaging suggested a 2.5 mm calculus in the distal right ureter and hydronephrosis; however, ureteroscopy revealed a large fleshy mass at the location. Histopathologic evaluation demonstrated the lesion to be primary small cell carcinoma of the ureter, without evidence of it being a derivative of the prior gynecologic malignancy. Metastatic work-up revealed high burden retroperitoneal adenopathy. The patient was started on Cisplatin-based neoadjuvant chemotherapy with plan for nephroureterectomy in the future. At 3 months follow-up, the patient was doing well with significant shrinkage of retroperitoneal adenopathy and no evidence of disease progression.
上尿路原发性神经内分泌肿瘤极为罕见。我们报告一例输尿管小细胞癌,其表现为伪装成远端输尿管结石。一名55岁女性因右下背部疼痛和血尿1个月就诊于我们的诊所。她的病史值得注意的是,7年前在本次发病前,曾因1B期子宫混合性透明细胞-子宫内膜样癌接受根治性腹部子宫切除及辅助放疗,目前患者无复发证据。最初的非增强成像显示右输尿管远端有一个2.5毫米的结石及肾积水;然而,输尿管镜检查发现该部位有一个大的肉质肿块。组织病理学评估显示该病变为原发性输尿管小细胞癌,无证据表明其是先前妇科恶性肿瘤的衍生物。转移灶检查发现腹膜后淋巴结肿大严重。患者开始接受以顺铂为基础的新辅助化疗,计划未来进行肾输尿管切除术。在3个月的随访中,患者情况良好,腹膜后淋巴结明显缩小,无疾病进展迹象。