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难治性重症肌无力的处理 被引量:5

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摘要 大约10%的重症肌无力(MG)属于难治性,明确难治性MG有助于及时换用有效的免疫治疗,控制病情。目前难治性MG还缺乏比较统一的定义。判断难治性MG需要经过一定的流程,并进行鉴别诊断和病理生理诊断。判断为难治性MG后,在调整病理生理状况的基础上选择更强的免疫抑制剂治疗才能有效控制病情并取得较好的长期疗效。
作者 李海峰
出处 《中国神经免疫学和神经病学杂志》 CAS 2009年第1期61-64,共4页 Chinese Journal of Neuroimmunology and Neurology
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