Gohji K, Nakanishi T, Hara I, Hamami G, Kamidono S
J Urol. 1987 May;137(5):966-8. doi: 10.1016/s0022-5347(17)44313-8.
Primary neuroblastoma of the kidney in adults is an extremely rare neoplasm that had not been described in the literature until 1986. The diagnosis can be made by histopathological examination only. We report 2 unusual cases of neuroblastoma of the kidney in adults. In both patients right nephrectomy was performed after the diagnosis of right renal cell carcinoma was made. Histological examination revealed the tumors to be primary neuroblastomas of the right kidney. In the first patient cobalt therapy was administered to the tumor bed and para-aortic area. Followup at 5 years revealed no sign of tumor recurrence. Progressive disseminated disease has been documented in the second patient despite postoperative adjuvant chemotherapy with combined cis-platinum and epipodophyllotoxin, and combined vincristine, cyclophosphamide, doxorubicin and dimethyl-tri-azeno imidazole carboxamine.
成人原发性肾神经母细胞瘤是一种极为罕见的肿瘤,直到1986年才在文献中有所描述。其诊断只能通过组织病理学检查来确定。我们报告2例成人肾神经母细胞瘤的罕见病例。两名患者在被诊断为右肾细胞癌后均接受了右肾切除术。组织学检查显示肿瘤为右肾原发性神经母细胞瘤。第一例患者对肿瘤床和腹主动脉旁区域进行了钴治疗。5年随访未发现肿瘤复发迹象。尽管第二例患者术后接受了顺铂和依托泊苷联合以及长春新碱、环磷酰胺、多柔比星和达卡巴嗪联合辅助化疗,但仍有疾病进展和播散的记录。