Neuroinflammatory Disease following Severe Acute Respiratory Syndrome Coronavirus 2 Infection in Children

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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 | Zhang, Shen-Ying | Boddaert, Nathalie | Desguerre, Isabelle

Edité par CCSD ; Elsevier -

International audience. ObjectiveTo 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.Study designWe focused on CNS inflammatory diseases in children referred from 12 hospitals in the Paris area to Necker-Sick Children Reference Centre.ResultsWe 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.ConclusionsSARS2-CoV-2 represents a new trigger of postinfectious CNS inflammatory diseases in children.

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