Idiopathic autoimmune encephalitis with a recurrent course. A case report

A. B. Davletova, A. Y. Ryabchenko
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Abstract

We presented a clinical case of idiopathic autoimmune brainstem encephalitis in a 12-year-old female patient. At the onset of the disease, which developed after a respiratory infection, the clinical picture was accompanied by oculomotor and bulbar syndromes. The diagnosis of Bickerstaff brainstem encephalitis was made based on clinical diagnostic criteria and the positive effect of the course of intravenous immunoglobulin therapy. During 3 years of follow-up, there were periods of relapse of the disease, during which symptoms not typical for Bickerstaff stem encephalitis appeared. Against the background of long-term immunosuppressive therapy, there was a long-term remission of about 2 years. The clinical picture, the presence of relapses, the data of additional methods forced to reconsider the diagnosis in favor of idiopathic autoimmune brainstem encephalitis.
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复发的特发性自身免疫性脑炎。病例报告
我们报告了一个12岁的女性特发性自身免疫性脑干脑炎的临床病例。在疾病的发病,这是发展后的呼吸道感染,临床表现是伴随着动眼病和球综合征。根据临床诊断标准和静脉注射免疫球蛋白治疗过程的积极效果,诊断为比克斯塔夫脑干脑炎。在3年的随访中,有疾病复发的时期,在此期间出现了比克斯塔夫脑炎不典型的症状。在长期免疫抑制治疗的背景下,有大约2年的长期缓解。临床表现,复发的存在,其他方法的数据迫使重新考虑支持特发性自身免疫性脑干脑炎的诊断。
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