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    李青, 于露, 陈浩, 张作慧, 胡倩, 郑惠文, 陈雪婷, 刘永海. 自身免疫性脑炎的临床特征分析[J]. 徐州医科大学学报, 2020, 40(2): 103-107.
    引用本文: 李青, 于露, 陈浩, 张作慧, 胡倩, 郑惠文, 陈雪婷, 刘永海. 自身免疫性脑炎的临床特征分析[J]. 徐州医科大学学报, 2020, 40(2): 103-107.
    Clinical and imaging characteristics of Autoimmune encephalitis[J]. Journal of Xuzhou Medical University, 2020, 40(2): 103-107.
    Citation: Clinical and imaging characteristics of Autoimmune encephalitis[J]. Journal of Xuzhou Medical University, 2020, 40(2): 103-107.

    自身免疫性脑炎的临床特征分析

    Clinical and imaging characteristics of Autoimmune encephalitis

    • 摘要: 目的:探讨自身免疫性脑炎的临床特点及治疗预后。方法:收集2016年6月至2019年10月于徐州医科大学附属医院确诊的自身免疫性脑炎患者19例。回顾性分析其临床表现、脑脊液检查、影像学、脑电图检查及治疗预后。结果:1.19例患者中男女比例为14:5,年龄18~68岁,平均年龄42.1±16.0岁。2.起病形式多呈急性或亚急性,临床表现:癫痫发作13例,精神行为异常11例,认知障碍10例,言语障碍4例,意识水平的下降或昏迷4例,自主神经功能障碍3例,睡眠障碍3例,中枢性低通气3例,腹泻1例,低钠血症1例。3.脑脊液检查:脑脊液白细胞数增高者18例,蛋白增高者10例,免疫球蛋白IgG增高者11例,液基细胞学见淋巴细胞增多者7例。4.影像学:头颅MRI检查主要表现为额叶、颞叶、海马、岛叶等部位T2WI、FLAIR呈高信号,部分患者DWI呈高信号,增强扫描伴强化者少见。脑电图:正常者6例,轻度异常者5例,中度异常者4例,重度异常者1例。5.治疗预后:多数患者使用糖皮质激素、免疫球蛋白等免疫治疗后MRS评分较入院时降低1-3分,症状完全恢复者6例,放弃治疗者1例。结论:自身免疫性脑炎临床表现复杂多样,临床工作中遇到以癫痫发作、精神行为异常、认知障碍症状急性或亚急性起病的患者,应考虑自身免疫性脑炎可能,需完善脑脊液、头颅MRI等相关检查,尽早启动免疫治疗。

       

      Abstract: ob<x>jective To investigate the clinical and imaging features of Autoimmune encephalitis Methods A total of 19 patients who were with diagnosed as autoimmune encephalitis in the affiliated hospital of Xuzhou Medical University from June 2016 to October 2019 were enrolled in this study.Their clinical manifestations, cerebrospinal fluid examination, imaging, EEG examination and treatment prognosis were retrospectively analyzed..Results 1.Among the 19 patients , 14 were male and 5 were female, aged 18 to 68 years, with an average age of 42.1 ± 16.0 years.2.Clinical manifestations:13 cases of seizures, 11 cases of mental and behavioral disorders, 10 cases of cognitive impairment, 4 cases of speech disorder, 4 cases of decreased consciousness or coma, 3 cases of autonomic dysfunction, 3 cases of sleep disorder, 3 cases of central hypoventilation , 1 case of diarrhea and 1 case of hyponatremia.3.Cerebrospinal fluid examination: 18 cases of increased white blood cell count, 10 cases of increased protein, 11 cases of increased immunoglobulin IgG and 7 cases of lymphocytosis.4.Imaging features: The head MRI examination mainly showed high signal in T2WI and FLAIR in frontal lobe, temporal lobe, hippocampus, and island lobe, and some patients showed high signal in DWI. It is rare for enhanced scan with intensive scan.EEG: 6 cases were normal, 5 cases were mildly abnormal, 4 cases were moderately abnormal, and 1 case was severely abnormal.5.Treatment and prognosis: Most patients received glucocorticoids, immunoglobulins and other immunotherapy treatments, and their MRS scores were lower by 1-3 points than admitted to the hospital. Six patients recovered completely, and one patient abandoned treatment.Conclusion The clinical manifestations of autoimmune encephalitis are complex and diverse. In clinical work, patients with acute or subacute onset of epileptic seizures, mental and behavioral abnormalities and cognitive disorders should consider the possibility of autoimmune encephalitis, improve cerebrospinal fluid, brain MRI and start immunotherapy as soon as possible.

       

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