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Clinical diagnosis and treatment of pediatric anti-N-methyl-D-aspartate receptor encephalitis: A single center retrospective study

机译:小儿抗N-甲基-D-天冬氨酸受体脑炎的临床诊断和治疗:单中心回顾性研究

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摘要

The aim of the present retrospective study was to investigate the diagnosis, treatment and prognosis of pediatric anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. A total of 23 pediatric patients with anti-NMDAR encephalitis were included in the present study. The clinical data, laboratory test results, imaging examination, treatment outcomes, and follow-up records were reviewed and analyzed. A total of 8 patients exhibited prodromal symptoms, including fever, cough, and vomiting. Clinical symptoms included epilepsy, convulsions, ataxia, coma, dyskinesia, personal behavior change and hallucinations. A total of 20 cases had the initial neurologic symptoms of dyskinesia or seizure, whereas 3 cases exhibited psychiatric symptoms of personal behavior change and hallucinations. Furthermore, pediatric patients >6 years old had more psychiatric symptoms than those ≤6 years. A total of 20 cases exhibited abnormal electroencephalography records, with 1 case of extreme δ brush. A total of 10 cases exhibited abnormal brain magnetic resonance imaging detection. Furthermore, the CSF protein contents for pediatric patients ≤6 years old was significantly higher than those >6 years. For treatment, 18 pediatric patients received the first-line treatment of methylprednisone and intravenous injection of immunoglobulin, and 6 cases were subjected to the second-line treatment of rituximab. A total of 2 patients underwent plasma exchange and/or cyclophosphamide treatment. In follow-up, 12 cases reported no convulsion, whereas 11 cases had moderate or severe neurological and psychiatric sequelae. The recovery rate for pediatric patients ≤6 years old was significantly higher than those >6 years. Anti-NMDAR encephalitis is commonly seen in pediatric patients, mainly with initial neurological symptoms. These patients could respond to immunotherapy, and younger pediatric patients typically have a better prognosis.
机译:这项回顾性研究的目的是调查小儿抗N-甲基-D-天冬氨酸受体(抗NMDAR)脑炎的诊断,治疗和预后。本研究共纳入23名小儿抗NMDAR脑炎患者。回顾和分析了临床数据,实验室检查结果,影像学检查,治疗结果和随访记录。共有8例患者出现前驱症状,包括发烧,咳嗽和呕吐。临床症状包括癫痫,抽搐,共济失调,昏迷,运动障碍,个人行为改变和幻觉。共有20例具有运动障碍或癫痫发作的初始神经系统症状,而3例表现出个人行为改变和幻觉的精神病症状。此外,> 6岁的儿科患者比≤6岁的患者有更多的精神症状。共有20例脑电图记录异常,其中1例刷牙为δ。共有10例表现出异常的脑磁共振成像检测。此外,≤6岁的小儿CSF蛋白含量显着高于> 6岁的小儿。为治疗,18名儿科患者接受了甲泼尼龙一线治疗并静脉注射免疫球蛋白,6例接受了利妥昔单抗二线治疗。共有2例患者接受了血浆置换和/或环磷酰胺治疗。在随访中,有12例未报告惊厥,而11例有中度或严重神经和精神病后遗症。 ≤6岁的儿科患者的康复率显着高于> 6岁的儿科患者。抗NMDAR脑炎常见于小儿患者,主要表现为最初的神经系统症状。这些患者可能对免疫疗法有反应,而年轻的儿科患者通常预后较好。

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