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作 者:Adhasit Nawa‑apisak Saharat Aungsumart Metha Apiwattanakul
机构地区:[1]Department of Neurology,Neuroimmunology Unit,Prasat Neurological Institute,Bangkok 10400,Thailand
出 处:《Neuroimmunology and Neuroinflammation》2016年第1期79-85,共7页神经免疫与神经炎症(英文版)
摘 要:Anti-N-methyl-D-aspartate receptor(NMDAR)encephalitis has been increasingly recognized in recent years.This condition may be the most common cause of antibody-mediated encephalitis worldwide.The majority of patients are young at the time of onset,female,and present with an acute-to-subacute onset of behavioral changes followed by seizure,abnormal movement,autonomic dysfunction,and finally hypoventilation with coma if left untreated.The immunopathogenesis of this disease may be due to antibody-mediated internalization of NMDARs from synapses,which results in the dysfunction of particular brain regions(especially the hippocampus and frontostriatal area).Compared to serum,the cerebrospinal fluid permits the more sensitive detection of anti-NMDAR antibody.Ovarian teratoma may be present in up to 40%of patients but is less frequent in children or late-onset disease(>45 years old).The severity at the time of disease onset and time to appropriate immunotherapy(high-dose steroid plus plasmapheresis or intravenous immunoglobulin)are independent factors that are associated with good outcomes.
关 键 词:Abnormal movement anti-N-methyl-D-aspartate receptors encephalitis GLUTAMATE IMMUNOTHERAPY ovarian teratoma psychiatric symptoms SEIZURE
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