【摘要】 目的 :探讨家族性嗜铬细胞瘤的诊断和治疗方法。方法 :回顾性分析一家族三代 5例患者的临床资料 ,并复习相关文献。结果 :3例行肿瘤切除术 ,病理证实 ,术后症状消失 ,随访 6月至 2 8年无复发。 2例临床拟诊 ,其中 ,一例发作时院外死亡 ,另一例症状轻微 ,未经治疗。结论 :家族性嗜铬细胞瘤的典型症状是 :头痛、心悸、出汗、血压升高等 ,也可出现特殊症状 ,如 :心律失常、晕厥等。B超对该病的诊断有实用价值 ,手术切除是目前唯一有效的治疗方法更多还原

【Abstract】 Objective:To study the diagnosis and treatment of familial Pheochromocytoma.Methods:five patients with familial Pheochromocytoma of three generations in one kidnap were retrospectively analyzed,and connecting references were reviewed.Results:Three patients were operated on, and the diagnosis was verified by pathological examination.The symptoms were all disappeared after operation.All the patients were followed up for 6 months to-28 years,and there was no recurrence.Two patients were clinically suspected.one patient was sudden death while attacking outside,the other one has slight symptom,so accepted no operation.Conclusion:The typical symptom of familial Pheochromocytoma is headache, palpation,sweat, and high blood pressure.Special symptoms,for example,arrhythmia and syncope are also the character of the disease.B type ultrasonography shows practical value to the diagnosis of the disease.Operation is still the only way to cure it.更多还原