天津医药 ›› 2018, Vol. 46 ›› Issue (4): 376-380.doi: 10.11958/20171448

• 临床研究 • 上一篇    下一篇

六例自身免疫性脑炎的临床特征分析

毛汕,宋毅军△   

  1. 基金项目:天津市应用基础与前沿技术研究计划项目(14JCZDJC35400);2016年度天津市“131”创新型人才团队培养工程 作者单位:天津医科大学总医院神经内科,天津市神经病学研究所(邮编300052) 作者简介:毛汕(1992),女,硕士在读,主要从事癫痫的基础及临床研究 △通讯作者 E-mail: songyijun2000@126.com
  • 收稿日期:2017-12-15 修回日期:2018-01-30 出版日期:2018-04-15 发布日期:2018-04-15
  • 通讯作者: 宋毅军 E-mail:songyijun2000@126.com
  • 基金资助:
    天津市应用基础与前沿技术研究计划;2016年度天津市“131”创新型人才团队培养工程

Clinical analysis of autoimmune encephalitis of six cases

MAO Shan, SONG Yi-jun△   

  1. Department of Neurology, Tianjin Medical University General Hospital,Tianjin Neurological Institute, Tianjin 300052, China △Corresponding Author E-mail: songyijun2000@126.com
  • Received:2017-12-15 Revised:2018-01-30 Published:2018-04-15 Online:2018-04-15
  • Contact: yijun song E-mail:songyijun2000@126.com

摘要: 摘要:目的 探讨自身免疫性脑炎(AE)的临床特点、治疗与预后。方法 对我院收治的6例AE患者的临床表 现、实验室检查、治疗方法及预后等临床资料进行回顾性分析。结果 6例AE患者中,1例为抗N-甲基-D-天冬氨酸 受体(NMDAR)脑炎,2例为抗富含亮氨酸胶质瘤失活蛋白1(LGI1)抗体脑炎,3例为抗体阴性AE。以痫性发作(6/ 6)、意识水平下降(5/6)、近事记忆力下降的认知功能障碍(4/6)、精神和行为异常(3/6)为主要临床表现。所有患者的 颅脑MRI结果均可及异常信号,以边缘系统受累为主;脑电图多表现为弥散性慢波节律,异常放电以颞区为著(3/6); 脑脊液检查提示乳酸脱氢酶增多(4/6)。患者入院后5例接受了糖皮质激素冲击治疗,其中3例联合静脉注射免疫球 蛋白。所有患者均好转出院,但均遗留癫痫。结论 以痫性发作伴意识水平下降、认知功能障碍及精神和行为异常 为主要临床表现的患者,要警惕AE的可能,急性期治疗建议采用糖皮质激素并联合静脉注射免疫球蛋白冲击治疗, 后期遗留癫痫可能性较大。

关键词: 脑炎, 预后, 自身免疫性脑炎, 临床特点, 治疗

Abstract: Abstract: Objective To analyze the clinical characteristics and prognosis of patients with autoimmune encephalitis (AE). Methods The clinical manifestations, laboratory examination, treatment methods and prognosis of patients admitted to our hospital were retrospectively analyzed. Results Of 6 AE patients in this study, one of them was diagnosed as anti-N methyl-D-aspartate receptor (NMDAR) encephalitis, two were anti-leucine-rich glioma-inactivated 1 (LGI1) encephalitis, and 3 were autoimmune perpheral encephalitis with antibody-negative. The main clinical manifestations were seizure (6/6), decreased consciousness (5/6), cognitive impairment in the decline of memory (4/6) and mental and behavioral abnormalities (3 / 6). All of them (6 / 6) had abnormal brain MRI signals, mainly with the involvement of the marginal system. The electroencephalogram (EEG) was characterized by diffuse slow wave rhythm, especially in temporal lobe (3/6). Cerebrospinal fluid examination showed the increased lactate dehydrogenase (4 / 6). Five patients received glucocorticoid therapy, three received intravenous immunoglobulin. All patients were improved and discharged, but all were left with epilepsy. Conclusion In patients with major clinical manifestations of epileptic seizures with decreased consciousness, cognitive dysfunction and mental and behavioral abnormalities, the possibility of AE should be vigilant. It is suggested that the use of glucocorticoid and intravenous immunoglobulin protein in the acute stage of AE for impact therapy, and should pay attention to control the seizures.

Key words: encephalitis, prognosis, autoimmune encephalitis, clinical features, treatment