Gough Jessica L, Coebergh Jan, Chandra Brunda, Nilforooshan Ramin
Jessica L Gough, Jan Coebergh, St Peter's Hospital, Chertsey, Surrey, KT16 0PZ, United Kingdom.
World J Clin Cases. 2016 Aug 16;4(8):223-8. doi: 10.12998/wjcc.v4.i8.223.
Autoimmune encephalitis is a poorly understood condition that can present with a combination of neurological and psychiatric symptoms, either of which may predominate. There are many autoantibodies associated with a variety of clinical syndromes - anti-N-Methyl-D-Aspartate receptor (NMDAR) is the commonest. Currently, the most widely used therapy is prompt plasmapheresis and steroid treatment (and tumour resection if indicated), followed by second line immunosuppression if this fails. Given the growing awareness of autoimmune encephalitis as an entity, it is increasingly important that we consider it as a potential diagnosis in order to provide timely, effective treatment. We discuss several previously published case reports and one new case. These reports examined the effects of electroconvulsive therapy (ECT) on patients with autoimmune encephalitis, particularly those in whom psychiatric symptoms are especially debilitating and refractory to standard treatment. We also discuss factors predicting good outcome and possible mechanisms by which ECT may be effective. Numerous cases, such as those presented by Wingfield, Tsutsui, Florance, Sansing, Braakman and Matsumoto, demonstrate effective use of ECT in anti-NMDAR encephalitis patients with severe psychiatric symptoms such as catatonia, psychosis, narcolepsy and stupor who had failed to respond to standard treatments alone. We also present a new case of a 71-year-old female who presented to a psychiatric unit initially with depression, which escalated to catatonia, delusions, nihilism and auditory hallucinations. After anti-NMDAR antibodies were isolated, she was treated by the neurology team with plasmapheresis and steroids, with a partial response. She received multiple sessions of ECT and her psychiatric symptoms completely resolved and she returned to her premorbid state. For this reason, we suggest that ECT should be considered, particularly in those patients who are non-responders to standard therapies.
自身免疫性脑炎是一种人们了解甚少的疾病,可表现为神经和精神症状的组合,其中任何一种症状都可能占主导。有许多自身抗体与多种临床综合征相关——抗N-甲基-D-天冬氨酸受体(NMDAR)抗体最为常见。目前,最广泛使用的治疗方法是及时进行血浆置换和类固醇治疗(如有指征则进行肿瘤切除),如果治疗失败则进行二线免疫抑制治疗。鉴于人们越来越认识到自身免疫性脑炎是一种独立的疾病,我们将其视为潜在诊断以提供及时、有效的治疗变得越来越重要。我们讨论了几篇先前发表的病例报告和一个新病例。这些报告研究了电休克治疗(ECT)对自身免疫性脑炎患者的影响,特别是那些精神症状特别严重且对标准治疗无效的患者。我们还讨论了预测良好预后的因素以及ECT可能有效的潜在机制。许多病例,如温菲尔德、津木、弗洛兰斯、桑辛、布拉克曼和松本报道的病例,都证明了ECT在患有严重精神症状(如紧张症、精神病、发作性睡病和木僵)且对单独标准治疗无反应的抗NMDAR脑炎患者中的有效应用。我们还介绍了一名71岁女性的新病例,她最初因抑郁症入住精神科病房,随后病情发展为紧张症、妄想、虚无主义和幻听。分离出抗NMDAR抗体后,神经科团队对她进行了血浆置换和类固醇治疗,症状部分缓解。她接受了多次ECT治疗,精神症状完全缓解,恢复到病前状态。因此,我们建议应考虑使用ECT,特别是对于那些对标准治疗无反应的患者。