Aubart Melodie, Roux Charles-Joris, Durrleman Chloé, Gins Clarisse, Hully Marie, Kossorotoff Manoelle, Gitiaux Cyril, Levy Raphaël, Moulin Florence, Debray Agathe, Belhadjer Zahra, Georget Emilie, Kom Temi, Blanc Philippe, Wehbi Samer, Mazeghrane Mustapha, Tencer Jeremie, Gajdos Vincent, Rouget Sebastien, De Pontual Loic, Basmaci Romain, Yacouben Karima, Angoulvant Francois, Leruez-Ville Marianne, Sterlin Delphine, Rozenberg Flore, Robert Matthieu P, Zhang Shen-Ying, Boddaert Nathalie, Desguerre Isabelle
Pediatric Neurology Department, Necker-Enfants malades Hospital, APHP, University of Paris-Cité, Paris, France; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, French Institute of Health and Medical Research U1163, University of Paris-Cité, Imagine Institute, Paris, France.
Pediatric Radiology Department, Necker-Enfats malades Hospital, APHP, University of Paris-Cité, Paris, France.
J Pediatr. 2022 Aug;247:22-28.e2. doi: 10.1016/j.jpeds.2022.05.018. Epub 2022 May 14.
To describe neurologic, radiologic and laboratory features in children with central nervous system (CNS) inflammatory disease complicating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.
We focused on CNS inflammatory diseases in children referred from 12 hospitals in the Paris area to Necker-Sick Children Reference Centre.
We identified 19 children who had a history of SARS-CoV-2 infection and manifest a variety of CNS inflammatory diseases: encephalopathy, cerebellar ataxia, acute disseminated encephalomyelitis, neuromyelitis optica spectrum disorder, or optic neuritis. All patients had a history of SARS-CoV-2 exposure, and all tested positive for circulating antibodies against SARS-CoV-2. At the onset of the neurologic disease, SARS-CoV-2 PCR results (nasopharyngeal swabs) were positive in 8 children. Cerebrospinal fluid was abnormal in 58% (11/19) and magnetic resonance imaging was abnormal in 74% (14/19). We identified an autoantibody co-trigger in 4 children (myelin-oligodendrocyte and aquaporin 4 antibodies), representing 21% of the cases. No autoantibody was found in the 6 children whose CNS inflammation was accompanied by a multisystem inflammatory syndrome in children. Overall, 89% of patients (17/19) received anti-inflammatory treatment, primarily high-pulse methylprednisolone. All patients had a complete long-term recovery and, to date, no patient with autoantibodies presented with a relapse.
SARS2-CoV-2 represents a new trigger of postinfectious CNS inflammatory diseases in children.
描述患有中枢神经系统(CNS)炎症性疾病并伴有严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的儿童的神经、放射学和实验室特征。
我们重点关注从巴黎地区12家医院转诊至内克尔儿童医院参考中心的儿童中枢神经系统炎症性疾病。
我们确定了19名有SARS-CoV-2感染病史且表现出多种中枢神经系统炎症性疾病的儿童:脑病、小脑共济失调、急性播散性脑脊髓炎、视神经脊髓炎谱系障碍或视神经炎。所有患者都有SARS-CoV-2暴露史,并且所有患者针对SARS-CoV-2的循环抗体检测均呈阳性。在神经疾病发作时,8名儿童的SARS-CoV-2 PCR结果(鼻咽拭子)呈阳性。脑脊液异常的占58%(11/19),磁共振成像异常的占74%(14/19)。我们在4名儿童中发现了自身抗体共同触发因素(髓鞘少突胶质细胞和水通道蛋白4抗体),占病例的21%。在6名中枢神经系统炎症伴有儿童多系统炎症综合征的儿童中未发现自身抗体。总体而言,89%的患者(17/19)接受了抗炎治疗,主要是大剂量脉冲甲基强的松龙。所有患者均实现了长期完全康复,迄今为止,没有自身抗体阳性的患者复发。
SARS-CoV-2是儿童感染后中枢神经系统炎症性疾病的新触发因素。