嗜铬细胞瘤(Pheochromocytoma)随诊疗技术手段的提高,迄今已屡见不鲜,本院收集自1979年～1991年经手术且有病理证实的肾上腺嗜铬细胞瘤12例,结合临床及文献复习予以讨论。临床资料男性5例,女性7例,男女之比1:1.4,年龄25岁～65岁,中位年龄41岁,病史1年～2年,发生部位均在肾上腺,右侧者8例,左侧者4例,CT和B超定位诊断提示肾上腺占位病变。 Pheochromocytoma (Pheochromocytoma) has become commonplace with the advancement of diagnostic and therapeutic techniques. Our hospital has collected 12 cases of adrenal pheochromocytoma confirmed by pathology from 1979 to 1991, combined with clinical and literature review. Clinical data were 5 males and 7 females. The male to female ratio was 1:1.4, the age ranged from 25 to 65 years, the median age was 41 years, and the medical history was from 1 year to 2 years. The site of the disease was in the adrenal gland and the right side was in 8 cases. Left In 4 cases, CT and B-ultrasound diagnosis suggested adrenal mass lesions.