作者报告上海第一医学院附属第一医院及中山医院泌尿科自1953年1月至1962年12月止10年内对8例嗜铬细胞瘤患者手术治疗的经过。其中肾上腺嗜铬细胞瘤6例,肾上腺外腹膜后嗜铬细胞瘤1例,胸内及椎陶孔内1例。除1例系恶性外,其余7例均属良性。8例中5例经手术切除后已彻底治愈,1例恶性肿瘤因无法根治,采用姑息性放射治疗,随访二年余尚生存。2例手术死亡。本病的临床表现是以高血压和代谢紊乱为主,除极少数病例可能没有症状外,—般分二型;(1)阵 The authors report the surgical treatment of 8 pheochromocytoma patients in the Department of Urology of the First Affiliated Hospital of Shanghai First Medical College and Zhongshan Hospital from January 1953 to December 1962. Among them, there were 6 cases of adrenal pheochromocytomas, 1 case of adrenal extraperitoneal pheochromocytoma, and 1 case of intrathoracic and vertebral holes. Except one case was malignant, the remaining seven cases were all benign. Five of the eight cases had been completely cured after surgical resection. One case of malignant tumor could not be cured. Palliative radiation therapy was used. It survived more than two years after follow-up. Two patients died of surgery. The clinical manifestations of the disease are mainly hypertension and metabolic disorders, except for a very small number of cases that may have no symptoms. They are generally divided into two types; (1)