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The SCARE 2020 Guideline: Updating Consensus Surgical CAse REport (SCARE) Guidelines.SCARE 2020 指南:更新共识手术病例报告(SCARE)指南。
Int J Surg. 2020 Dec;84:226-230. doi: 10.1016/j.ijsu.2020.10.034. Epub 2020 Nov 9.
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Brain Behav Immun. 2020 Jul;87:179-181. doi: 10.1016/j.bbi.2020.05.054. Epub 2020 May 23.
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An update on anti-NMDA receptor encephalitis for neurologists and psychiatrists: mechanisms and models.神经科医生和精神科医生对抗 NMDA 受体脑炎的最新认识:发病机制和模型。
Lancet Neurol. 2019 Nov;18(11):1045-1057. doi: 10.1016/S1474-4422(19)30244-3. Epub 2019 Jul 17.
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Pediatric anti-NMDA receptor encephalitis with catatonia: treatment with electroconvulsive therapy.小儿抗N-甲基-D-天冬氨酸受体脑炎伴紧张症:电休克治疗
Pediatr Rheumatol Online J. 2019 Feb 18;17(1):8. doi: 10.1186/s12969-019-0310-0.
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Japanese Encephalitis Virus-Induced Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report and Review of Literature.日本脑炎病毒所致抗N-甲基-D-天冬氨酸受体脑炎:一例报告及文献复习
Neuropediatrics. 2019 Apr;50(2):111-115. doi: 10.1055/s-0038-1675607. Epub 2019 Jan 8.
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Anti-N-methyl-D-aspartate receptor encephalitis associated with acute Toxoplasma gondii infection: A case report.与急性弓形虫感染相关的抗N-甲基-D-天冬氨酸受体脑炎:一例报告。
Medicine (Baltimore). 2018 Feb;97(7):e9924. doi: 10.1097/MD.0000000000009924.
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Autoimmune Encephalitis.自身免疫性脑炎
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The growing spectrum of antibody-associated inflammatory brain diseases in children.儿童中与抗体相关的炎症性脑疾病谱不断扩大。
Neurol Neuroimmunol Neuroinflamm. 2015 Apr 2;2(3):e92. doi: 10.1212/NXI.0000000000000092. eCollection 2015 Jun.
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Anti-N-methyl-D-aspartate receptor-mediated encephalitis in infants and toddlers: case report and review of the literature.抗 N-甲基-D-天冬氨酸受体脑炎在婴儿和学步儿童中的表现:病例报告和文献复习。
Pediatr Neurol. 2014 Feb;50(2):181-4. doi: 10.1016/j.pediatrneurol.2013.10.002. Epub 2013 Oct 14.
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Psychiatric manifestations of anti-NMDA receptor encephalitis: neurobiological underpinnings and differential diagnostic implications.抗N-甲基-D-天冬氨酸受体脑炎的精神症状:神经生物学基础及鉴别诊断意义
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青少年非副肿瘤性抗N-甲基-D-天冬氨酸受体脑炎所致急性精神病且恢复良好:一例报告

Teenager with acute psychosis due to non-paraneoplastic anti-N-methyl-d-aspartate receptor encephalitis with a successful recovery: A case report.

作者信息

Chamlagain Rajan, Shah Sangam, Thapa Sangharsha, Basnet Madan, Kandel Bipin, Paudel Basanta Sharma, Dhital Roman, Pokhrel Apil, Khanal Pitambar, Paudel Sandip

机构信息

Institute of Medicine, Tribhuvan University, Maharajgunj, 44600, Nepal.

Kathmandu University School of Medical Sciences, Dhulikhel, Nepal.

出版信息

Ann Med Surg (Lond). 2022 Sep 28;82:104790. doi: 10.1016/j.amsu.2022.104790. eCollection 2022 Oct.

DOI:10.1016/j.amsu.2022.104790
PMID:36268402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9577962/
Abstract

INTRODUCTION

Anti NMDAR encephalitis is a neuropsychiatric syndromic disease caused by an immunological response. Acute behavioral changes, psychosis, and catatonia are common clinical manifestations, are seizures, amnesia, speech difficulties, dyskinesia, and autonomic dysregulation.

CASE PRESENTATION

We discuss the case of a 14-year-old girl who had psychotic symptoms and tested positive for anti-NMDAR antibodies.

DISCUSSION

Patients present with psychiatric symptoms such as delusions, hallucinations, agitation, changes in speech mania, disorganized thinking, catatonia, insomnia, and often seizures. Anti-NMDAR encephalitis should be suspected in teenage patient with acute psychotic symptoms and seizure episodes. A multidisciplinary treatment strategy is required.

CONCLUSION

The delayed treatment can lead to complications and delayed recovery complicating the disease process so multidisciplinary approach of treatment is necessary.

摘要

引言

抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种由免疫反应引起的神经精神综合征疾病。急性行为改变、精神病和紧张症是常见临床表现,还有癫痫发作、失忆、言语困难、运动障碍和自主神经调节异常。

病例介绍

我们讨论了一名14岁女孩的病例,她出现了精神病症状且抗NMDAR抗体检测呈阳性。

讨论

患者表现出妄想、幻觉、躁动、言语躁狂改变、思维紊乱、紧张症、失眠等精神症状,且常伴有癫痫发作。对于出现急性精神病症状和癫痫发作的青少年患者,应怀疑抗NMDAR脑炎。需要采取多学科治疗策略。

结论

治疗延迟会导致并发症并使恢复延迟,使疾病过程复杂化,因此多学科治疗方法是必要的。