本文报道我院12年内(1970—1982年)收治的25例嗜铬细胞瘤患者中的6例男性儿童患者。最小6岁,最大15岁,14岁1例,12岁3例。起病至就诊时间50天—2年不等。均无家族史。其临床表现与成人大体相似,但病情发展一般比成人迅速而严重。诊断也较成人困难,需仔细进行临床观察及配合特殊检查。 This article reports 6 out of 25 cases of male pediatric pheochromocytoma patients admitted to our hospital within 12 years (1970-1982). Minimum 6 years old, maximum 15 years old, 14 years old 1 case, 12 years old 3 cases. Onset to treatment time 50 days - 2 years. No family history. Its clinical manifestations are generally similar to those of adults, but the condition is generally faster and more severe than that of adults. The diagnosis is also more difficult than that of adults. Careful clinical observation and special examinations are required.