Uemura Motohide, Nakagawa Masahiro, Mukai Masatoshi, Kanno Nobufumi, Nishimura Kensaku, Miyoshi Susumu, Yoshida Kyotaro, Kawano Kiyoshi
Department of Urology, Osaka Rosai Hospital.
Hinyokika Kiyo. 2004 Jan;50(1):29-32.
A 34-year-old man was referred to our hospital for small lung nodules. An imaging study including a computed tomographic scan and magnetic resonance imaging showed bilateral lung tumors and huge mass arising from the lower pole of the right kidney as well. The patient underwent right radical nephrectomy in May 2002. Pathological examination revealed that the tumor was pheochromocytoma, which developed from extra-adrenal tissue. In 6 cycles of CVD systemic chemotherapy (Cyclophosphamide 750 mg/m2, Vincristine 1.4 mg/m2, Dacarbazine 600 mg/m2), the lung tumors were decreasing in size, and were removed by a surgical procedure in January 2003. Pathological examination revealed that the lung tumors were pheochromocytomas metastasized from the primary tumor. He is alive without evidence of disease 5 months after the lung operation.
一名34岁男性因肺部小结节被转诊至我院。包括计算机断层扫描和磁共振成像在内的影像学检查显示双侧肺部肿瘤,同时右肾下极也有巨大肿块。该患者于2002年5月接受了右肾根治性切除术。病理检查显示肿瘤为嗜铬细胞瘤,起源于肾上腺外组织。在6个周期的CVD全身化疗(环磷酰胺750 mg/m²、长春新碱1.4 mg/m²、达卡巴嗪600 mg/m²)过程中,肺部肿瘤体积逐渐缩小,并于2003年1月通过手术切除。病理检查显示肺部肿瘤为原发肿瘤转移而来的嗜铬细胞瘤。肺部手术后5个月,他仍存活且无疾病迹象。