摘要
目的探讨POEMS综合征的临床特征。方法对15例POEMS综合征患者临床资料、相关检查及治疗方法进行回顾性研究。结果15例患者均有多发性神经病、淋巴结肿大、水肿、异常球蛋白血症及皮肤色素沉着,其他症状包括肝肿大6例、脾肿大9例、性功能障碍12例等。患者均予激素治疗,其中6例合用人血免疫球蛋白静滴。结论PO-EMS综合征是一种少见的多脏器损害疾病,诊断较难。临床上对可疑病例需进行密切观察及必要的检查,以免误诊。
Objective:To evaluate the clinical features of POEMS syndrome. Methods: The clinical materials of 15 pa tients with POEMS syndrome were analysed retrospectively. Results: All 15 patients presented polyneuropathy, enlargement of I.ymph Nodes, edema, abnormal globulinemia and hyperpigmented skin. 6 patients were complicated with hepatomegaly, 9 cases with splenomegalia and 12 cases with impotence. All were treated with corticoid, 6 with human immunoglobulin. Conclusions: POEMS syndrome was a rare disease with multiorgan involvement which made its diagnosis difficult. So suspected cases should be given close observation and taken necessary examination to avoid misdiagnosis.
出处
《脑与神经疾病杂志》
2006年第1期16-17,23,共3页
Journal of Brain and Nervous Diseases