肾上腺恶性嗜铬细胞瘤是发生在肾上腺髓质嗜铬细胞极为罕见的肿瘤,多见于40~50岁成人,常转移至淋巴结、骨、肝及肺等部位。因为发病率低,所以缺乏大样本的临床研究,目前尚无标准有效的治疗方法,5年生存率低于60%~[1],我科收治1例右肾上腺恶性嗜铬细胞瘤术后复发转移患者,予以多学科综合性治疗,总生存时间达7年,现总结经验和体会如下。资料与方法患者,男,51岁,2007年5月体检发现右肾上腺 Adrenal malignant pheochromocytoma is a very rare tumor occurring in adrenal medullary chromaffin cells, more common in adults 40 to 50 years old, often transferred to lymph nodes, bone, liver and lungs and other parts. Because of the low incidence, so the lack of a large sample of clinical studies, there is no standard and effective treatment, 5-year survival rate of less than 60% ~ [1], our department received a case of right adrenal malignant pheochromocytoma recurrence Transfer patients, to be comprehensive multidisciplinary treatment, the total survival time of up to 7 years, are summed up the experience and experience are as follows. Materials and Methods Patients, male, 51 years old, May 2007 physical examination found that the right adrenal