Department of Paediatric Neurology, Southampton University Hospital, Southampton, United Kingdom.
Eur J Paediatr Neurol. 2012 Jan;16(1):74-8. doi: 10.1016/j.ejpn.2011.07.005. Epub 2011 Aug 9.
We describe the clinical course and treatment of three unrelated female patients ranging in age from 27 months to 14 years with anti-NMDA receptor encephalitis. The third case is reported as an addendum to the paper. None of the cases were paraneoplastic. All received initial immunotherapy consisting of steroids and IVIg, and two of them received 3 and 8 plasma exchanges respectively, without consistent or sustained clinical improvement. All three girls were then treated with monthly cycles of Cyclophosphamide. All had resolution of their movement disorder and a dramatic and sustained clinical improvement of their other symptoms in the domains of cognition, language and behaviour. The clinical improvement began after the first cycle in two and the second cycle in the third and continued with the subsequent cycles. None developed side-effects of treatment. In light of the recent review of the condition and our own clinical experience in the paediatric age group, we propose that second line immunotherapy should be considered early after failure of first line immunotherapy.
我们描述了三例非相关女性抗 NMDA 受体脑炎患者的临床经过和治疗情况,年龄分别为 27 个月至 14 岁。第三例作为该论文的增刊报告。这些病例均无副肿瘤性。所有患者均接受初始免疫治疗,包括类固醇和 IVIg,其中 2 例分别接受了 3 次和 8 次血浆置换,但无一致或持续的临床改善。随后,这 3 名女孩均接受每月环磷酰胺周期治疗。所有患者的运动障碍均得到缓解,认知、语言和行为等其他症状也有显著和持续的临床改善。两名患者在第一个周期后开始改善,第三名患者在第二个周期后开始改善,且随着后续周期的继续而持续改善。所有患者均未出现治疗相关副作用。鉴于最近对该疾病的回顾和我们在儿科年龄组的临床经验,我们建议在一线免疫治疗失败后应尽早考虑二线免疫治疗。