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抗 N-甲基-D-天冬氨酸受体脑炎患儿的孤立性精神症状。

Isolated Psychiatric Symptoms in Children With Anti-N-Methyl-d Aspartate Receptor Encephalitis.

机构信息

Department of Pediatrics, Emory University SOM and Children's Healthcare of Atlanta, Atlanta, Georgia.

Division of Pediatric Neurology, Department of Neurology, University of Virginia Health System, Charlottesville, Virginia.

出版信息

Pediatr Neurol. 2024 Oct;159:12-15. doi: 10.1016/j.pediatrneurol.2024.07.009. Epub 2024 Jul 17.

Abstract

BACKGROUND

Isolated psychiatric symptoms can be the initial symptom of pediatric anti-N-methyl-d-aspartate (NMDA) receptor autoimmune encephalitis (pNMDARE). Here we report on the prevalence of isolated psychiatric symptoms in pNMDARE. We also assess whether initial neurodiagnostic tests (brain magnetic resonance imaging [MRI], electroencephalography [EEG], and/or cerebrospinal fluid [CSF] white blood cell count) are abnormal in children with isolated psychiatric symptoms and pNMDARE.

METHODS

This multicenter retrospective cohort study from CONNECT (Conquering Neuroinflammation and Epilepsies Consortium) from 14 institutions included children under age 18 years who were diagnosed with pNMDARE. Descriptive statistics using means, medians, and comparisons for continuous versus discrete data was performed.

RESULTS

Of 249 children included, 12 (5%) had only psychiatric symptoms without other typical clinical features of autoimmune encephalitis at presentation. All but one (11 of 12 = 92%) had at least one abnormal finding on initial ancillary testing: eight of 12 (67%) had an abnormal EEG, six of 12 (50%) had an abnormal MRI, and five of 12 (42%) demonstrated CSF pleocytosis. The single patient with a normal MRI, EEG, and CSF profile had low positive CSF NMDA antibody (titer of 1:1), and symptoms improved without immunotherapy.

CONCLUSIONS

Isolated first-episode psychiatric symptoms in pNMDARE are uncommon, and the majority of children will exhibit additional neurodiagnostic abnormalities. Delaying immunotherapy in a child with isolated psychiatric symptoms and normal neurodiagnostic testing may be warranted while awaiting confirmatory antibody testing.

摘要

背景

孤立性精神症状可能是儿科抗 N-甲基-D-天冬氨酸(NMDA)受体自身免疫性脑炎(pNMDARE)的首发症状。在此,我们报告孤立性精神症状在 pNMDARE 中的发生率。我们还评估了在仅有孤立性精神症状和 pNMDARE 的儿童中,初始神经诊断测试(脑磁共振成像[MRI]、脑电图[EEG]和/或脑脊液[CSF]白细胞计数)是否异常。

方法

这项来自 CONNECT(征服神经炎症和癫痫症联盟)的 14 家机构的多中心回顾性队列研究纳入了年龄在 18 岁以下被诊断为 pNMDARE 的儿童。使用均值、中位数和连续与离散数据的比较进行描述性统计。

结果

在纳入的 249 名儿童中,有 12 名(5%)在首发时仅有精神症状,没有自身免疫性脑炎的其他典型临床特征。除 1 名(11/12=92%)外,所有儿童在初始辅助检查中至少有 1 项异常发现:8/12(67%)的儿童 EEG 异常,6/12(50%)的儿童 MRI 异常,5/12(42%)的儿童 CSF 白细胞增多。唯一 MRI、EEG 和 CSF 特征正常的患者具有低滴度阳性 CSF NMDA 抗体(滴度为 1:1),且未经免疫治疗症状改善。

结论

孤立性首发精神病症状在 pNMDARE 中不常见,大多数儿童将表现出额外的神经诊断异常。在等待确认性抗体检测时,对仅有孤立性精神症状和神经诊断测试正常的儿童延迟免疫治疗可能是合理的。

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