Anti-NMDAR Encephalitis of 11 Cases in China - Detailed Clinical, Laboratory and Imagiological Description

脑炎 医学 自身免疫性脑炎 运动障碍 儿科 疾病 精神病 内科学 免疫学 精神科 帕金森病 病毒
作者
Junfeng Liu,Deren Wang,Yao Xiong,Bian Liu,Ming Liu
出处
期刊:European Neurology [Karger Publishers]
卷期号:74 (1-2): 73-78 被引量:8
标识
DOI:10.1159/000435953
摘要

<b><i>Background and Purpose:</i></b> Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a synaptic autoimmune disorder in which the auto-antibodies target NMDARs were first reported in 2007. Now, anti-NMDAR encephalitis is a widely recognized disease in the world. Our purpose was to analyze the clinical characteristics of anti-NMDAR encephalitis patients in West China Hospital in China and report the prognosis of the patients after accepting immunotherapy. <b><i>Methods:</i></b> Patients admitted to the West China Hospital who were diagnosed with anti-NMDAR encephalitis from 2013 to 2014 were retrospectively collected and their clinical features were analyzed. <b><i>Results:</i></b> We ultimately included 11 anti-NMDAR encephalitis patients. The median age of the 11 patients was 25 years, 46% patients were females, 27% patients were 15-18 years, and 73% patients were over 18 years. One of them was diagnosed with teratoma after discharging from hospital. The application of immunotherapy produced favorable outcomes in 67% patients included in our study. <b><i>Conclusions:</i></b> Anti-NMDAR encephalitis should be suspected in patients who developed a rapid change in behavior or psychosis, seizures, dyskinesia, and hypoventilation. Anti-NMDAR encephalitis is a kind of fatal but treatable disease. Timely diagnosis and treatment may yield favorable prognosis.

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