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多发性硬化为一种特定性地针对中枢Ns白质,导致其脱髓鞘的自身免疫疾病。有的病例症状和体征并不典型,也无典型的复发和缓解过程,易造成早期临床误诊,本文自1986年至1996年4月共收治的78例MS,其中不典型32例,现对其临床表现及CSF中出现寡克隆带,诱发电位异常及MRI在诊断中的作用做如下分析。 1 临床资料①一般资料:本组32例,男14例,女18例,年龄为17-52岁,其中17-20岁2例,20-30岁6
Multiple sclerosis is an autoimmune disease that is specifically targeted to central Ns white matter leading to its demyelination. Some cases of symptoms and signs are not typical, there is no typical process of relapse and remission, easily lead to early clinical misdiagnosis, this article from 1986 to April 1996 were treated 78 cases of MS, including atypical 32 cases, its Clinical manifestations and CSF oligoclonal bands appear, evoked potential abnormalities and MRI in the diagnosis of the role of the following analysis. 1 clinical data ① General Information: The group of 32 patients, 14 males and 18 females, aged 17-52 years, of which 17-20 years in 2 cases, 20-30 years of age 6