Pediatric MOG-Ab-Associated Encephalitis: Supporting Early Recognition and Treatment.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY Neurology® Neuroimmunology & Neuroinflammation Pub Date : 2024-12-01 Epub Date: 2024-10-11 DOI:10.1212/NXI.0000000000200323
Nee Na Kim, Dimitrios Champsas, Michael Eyre, Omar Abdel-Mannan, Vanessa Lee, Alison Skippen, Manali V Chitre, Rob Forsyth, Cheryl Hemingway, Rachel Kneen, Ming Lim, Dipak Ram, Sithara Ramdas, Evangeline Wassmer, Siobhan West, Sukhvir Wright, Asthik Biswas, Kshitij Mankad, Eoin P Flanagan, Jacqueline Palace, Thomas Rossor, Olga Ciccarelli, Yael Hacohen
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Abstract

Background and objectives: Antibodies to myelin oligodendrocyte glycoprotein (MOG-Ab) have recently been reported in patients with encephalitis who do not fulfill criteria for acute disseminated encephalomyelitis (ADEM). We evaluated a cohort of these children and compared them with children with ADEM.

Methods: This retrospective, multicenter cohort study comprised consecutive patients <18 years of age with MOG-Ab who fulfilled criteria for autoimmune encephalitis. These patients were stratified into (1) children not fulfilling criteria for ADEM (encephalitis phenotype) and (2) children with ADEM. Clinical/paraclinical data were extracted from the electronic records. Comparisons were made using the Mann-Whitney U test and χ2 Fisher exact test for statistical analysis.

Results: From 235 patients with positive MOG-Ab, we identified 33 (14%) with encephalitis and 74 (31%) with ADEM. The most common presenting symptoms in children with encephalitis were headache (88%), seizures (73%), and fever (67%). Infective meningoencephalitis was the initial diagnosis in 67%. CSF pleocytosis was seen in 79%. Initial MRI brain was normal in 8/33 (24%) patients. When abnormal, multifocal cortical changes were seen in 66% and unilateral cortical changes in 18%. Restricted diffusion was demonstrated in 43%. Intra-attack new lesions were seen in 7/13 (54%). When comparing with children with ADEM, children with encephalitis were older (median 8.9 vs 5.7 years, p = 0.005), were more likely to be admitted to intensive care (14/34 vs 4/74, p < 0.0001), were given steroid later (median 16.6 vs 9.6 days, p = 0.04), and were more likely to be diagnosed with epilepsy at last follow-up (6/33 vs 1/74, p = 0.003).

Discussion: MOG-Ab should be tested in all patients with suspected encephalitis even in the context of initially normal brain MRI. Although exclusion of infections should be part of the diagnostic process of any child with encephalitis, in immunocompetent children, when herpes simplex virus CSF PCR and gram stains are negative, these features do not preclude the diagnosis of immune mediated disease and should not delay initiation of first-line immunosuppression (steroids, IVIG, plasma exchange), even while awaiting the antibody results.

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小儿 MOG-Ab 相关脑炎:支持早期识别和治疗。
背景和目的:最近有报道称,不符合急性播散性脑脊髓炎(ADEM)标准的脑炎患者体内存在髓鞘少突胶质细胞糖蛋白(MOG-Ab)抗体。我们对这些儿童进行了评估,并与患有 ADEM 的儿童进行了比较:这项回顾性多中心队列研究由连续患者组成,采用 U 检验和 χ2 Fisher exact 检验进行统计分析:从 235 例 MOG-Ab 阳性的患者中,我们发现 33 例(14%)患有脑炎,74 例(31%)患有 ADEM。脑炎患儿最常见的症状是头痛(88%)、癫痫发作(73%)和发热(67%)。感染性脑膜脑炎是67%患儿的初步诊断。79%的患者出现脑脊液多细胞现象。8/33(24%)名患者的最初脑部核磁共振成像正常。如果出现异常,66%的患者出现多灶性皮质改变,18%的患者出现单侧皮质改变。43%的患者弥散受限。7/13(54%)的患者在发病时出现新的病变。与ADEM患儿相比,脑炎患儿年龄更大(中位数为8.9岁 vs 5.7岁,p = 0.005),更有可能入住重症监护室(14/34 vs 4/74,p < 0.0001),接受类固醇治疗的时间更晚(中位数为16.6天 vs 9.6天,p = 0.04),最后一次随访时更有可能被诊断为癫痫(6/33 vs 1/74,p = 0.003):讨论:所有疑似脑炎患者都应进行 MOG-Ab 检测,即使最初的脑磁共振成像正常。虽然排除感染应该是所有脑炎患儿诊断过程的一部分,但对于免疫功能正常的患儿,当单纯疱疹病毒CSF PCR和革兰染色阴性时,这些特征并不能排除免疫介导疾病的诊断,即使在等待抗体结果期间,也不应延迟一线免疫抑制(类固醇、IVIG、血浆置换)的启动。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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