嗜铬细胞瘤危象症状复杂,病情凶险,易致死亡。我院于1982年遇到一例,抢救成功,现报道如下。病历摘要患者,女,14岁,因发作性头痛4月余,头痛加剧伴血压剧烈波动一天,于1982年7月6日入院。患者自1982年2月开始发作性两颞侧隐痛,持续数秒至数分钟即自行缓解,初为数日发作一次,以后发作渐见频 Pheochromocytoma is a complex crisis with dangerous conditions and is prone to death. In 1982, our hospital encountered one case and the rescue was successful. The report is as follows. Medical records Abstract: The patient, female, was 14 years old. She suffered from severe headache for more than four months, and his headache increased with severe fluctuations in blood pressure. He was admitted to the hospital on July 6, 1982. The patient developed paroxysmal bilateral parotid pain in February 1982 and relieved spontaneously for several seconds to several minutes. The first episode lasted for several days, after which the episode gradually became visible.