Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age

Detalhes bibliográficos
Autor(a) principal: Branco, Mariana Amorim
Data de Publicação: 2019
Outros Autores: Sousa, Luísa, Garrido, Cristina, Carrilho, Inês, Santos, Manuela, Temudo, Teresa, Martins Silva, Ana, Figueiroa, Sónia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.25753/BirthGrowthMJ.v28.i2.14322
Resumo: Introduction: Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an immune-mediated syndrome characterized by psychiatric symptoms, movement disorders, insomnia, seizures, altered level of consciousness and autonomic dysfunction. The aim of this study was described the cases of anti-NMDAR encephalitis admitted to a Neuropediatrics Department, in order to alert for the importance of early recognition of this clinical entity due to its implications in prognosis. Material and Methods: A retrospective review of the clinical processes of patients with anti-NMDAR encephalitis admitted to the Neuropediatrics Department of a University Hospital in the period between May 2009 and May 2016 was conducted. Results: Diagnosis of anti-NMDAR encephalitis was established in nine patients. Mean age at diagnosis was 9.4 years and five patients were male. Most cases (88.9%) presented with neuropsychiatric symptomatology. Movement disorders were another frequent finding (88.9%) and include chorea, dystonia and dyskinesias. Altered level of consciousness occurred in 77.8% of cases, insomnia and speech disturbance in 66.7%, seizures in 55.6% and autonomic dysfunction in 22.2%. Anti-NMDAR antibodies were identified in the cerebrospinal fluid of all patients. One patient had an underlying neoplasm. All patients underwent immunosuppressive therapy and seven patients fully recovered. In the remaining patients, sequelae included refractory epilepsy and cognitive impairment. Discussion: The diagnosis of anti-NMDAR encephalitis should be considered in children and adolescents presenting with psychiatric symptoms associated and movement disorders. In this sample, although most patients responded very favorably to treatment, severe sequelae were also observed. This highlights the importance of an early diagnosis to initiate treatment as soon as possible.
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spelling Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric ageEncefalite anti-recetor N-metil-D-aspartato em idade pediátricaOriginal ArticlesIntroduction: Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an immune-mediated syndrome characterized by psychiatric symptoms, movement disorders, insomnia, seizures, altered level of consciousness and autonomic dysfunction. The aim of this study was described the cases of anti-NMDAR encephalitis admitted to a Neuropediatrics Department, in order to alert for the importance of early recognition of this clinical entity due to its implications in prognosis. Material and Methods: A retrospective review of the clinical processes of patients with anti-NMDAR encephalitis admitted to the Neuropediatrics Department of a University Hospital in the period between May 2009 and May 2016 was conducted. Results: Diagnosis of anti-NMDAR encephalitis was established in nine patients. Mean age at diagnosis was 9.4 years and five patients were male. Most cases (88.9%) presented with neuropsychiatric symptomatology. Movement disorders were another frequent finding (88.9%) and include chorea, dystonia and dyskinesias. Altered level of consciousness occurred in 77.8% of cases, insomnia and speech disturbance in 66.7%, seizures in 55.6% and autonomic dysfunction in 22.2%. Anti-NMDAR antibodies were identified in the cerebrospinal fluid of all patients. One patient had an underlying neoplasm. All patients underwent immunosuppressive therapy and seven patients fully recovered. In the remaining patients, sequelae included refractory epilepsy and cognitive impairment. Discussion: The diagnosis of anti-NMDAR encephalitis should be considered in children and adolescents presenting with psychiatric symptoms associated and movement disorders. In this sample, although most patients responded very favorably to treatment, severe sequelae were also observed. This highlights the importance of an early diagnosis to initiate treatment as soon as possible.Introdução: A encefalite anti-recetor N-metil-D-aspartato (NMDAR) é uma síndrome imunomediada, que se caracteriza por sintomas psiquiátricos, distúrbios do movimento, insónia, crises epiléticas, alterações do estado de consciência e instabilidade autonómica. O objetivo deste estudo foi efetuar uma descrição dos casos de encefalite anti-receptor N-metil-D-aspartato admitidos no Serviço de Neuropediatria, de modo a alertar para a importância do reconhecimento precoce desta entidade clínica devido às suas implicações prognósticas. Material e Métodos: Foi realizado um estudo retrospetivo com revisão dos processos clínicos dos doentes com diagnóstico de encefalite anti-NMDAR admitidos no Serviço de Neuropediatria de um Hospital Universitário no período entre maio de 2009 e maio de 2016. Resultados: Foi estabelecido o diagnóstico de encefalite anti-NMDAR em nove doentes. A idade média ao diagnóstico foi de 9,4 anos e cinco casos ocorreram no sexo masculino. A maioria dos casos (88,9%) apresentou sintomatologia neuropsiquiátrica. Distúrbios do movimento, caracterizados por coreia, distonia ou discinesias, foram igualmente frequentes (88,9%). Alterações do estado de consciência ocorreram em 77,8% dos casos, insónia e alterações na linguagem em 66,7%, crises epiléticas em 55,6% e sintomas disautonómicos em 22,2%. Em todos os doentes foram identificados anticorpos anti-NMDAR no líquido cefalorraquidiano. Um dos doentes apresentava uma neoplasia subjacente. Todos os doentes realizaram tratamento imunossupressor e sete recuperaram completamente. Os restantes doentes apresentaram sequelas que incluíram epilepsia refratária e alterações cognitivas. Discussão: O diagnóstico de encefalite anti-NMDAR deve ser considerado em crianças e adolescentes que apresentam sintomas psiquiátricos e distúrbios do movimento. Na presente amostra, embora a maioria dos doentes tenha respondido favoravelmente ao tratamento, também se verificou a ocorrência de sequelas graves. Com este trabalho, pretende reforçar-se a importância do diagnóstico precoce e instituição de terapêutica para esta entidade clínica.Centro Hospitalar Universitário do Porto2019-07-18T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25753/BirthGrowthMJ.v28.i2.14322eng2183-9417Branco, Mariana AmorimSousa, LuísaGarrido, CristinaCarrilho, InêsSantos, ManuelaTemudo, TeresaMartins Silva, AnaFigueiroa, Sóniainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-21T14:55:30Zoai:ojs.revistas.rcaap.pt:article/14322Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:56:26.857295Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
Encefalite anti-recetor N-metil-D-aspartato em idade pediátrica
title Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
spellingShingle Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
Branco, Mariana Amorim
Original Articles
title_short Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
title_full Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
title_fullStr Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
title_full_unstemmed Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
title_sort Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
author Branco, Mariana Amorim
author_facet Branco, Mariana Amorim
Sousa, Luísa
Garrido, Cristina
Carrilho, Inês
Santos, Manuela
Temudo, Teresa
Martins Silva, Ana
Figueiroa, Sónia
author_role author
author2 Sousa, Luísa
Garrido, Cristina
Carrilho, Inês
Santos, Manuela
Temudo, Teresa
Martins Silva, Ana
Figueiroa, Sónia
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Branco, Mariana Amorim
Sousa, Luísa
Garrido, Cristina
Carrilho, Inês
Santos, Manuela
Temudo, Teresa
Martins Silva, Ana
Figueiroa, Sónia
dc.subject.por.fl_str_mv Original Articles
topic Original Articles
description Introduction: Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an immune-mediated syndrome characterized by psychiatric symptoms, movement disorders, insomnia, seizures, altered level of consciousness and autonomic dysfunction. The aim of this study was described the cases of anti-NMDAR encephalitis admitted to a Neuropediatrics Department, in order to alert for the importance of early recognition of this clinical entity due to its implications in prognosis. Material and Methods: A retrospective review of the clinical processes of patients with anti-NMDAR encephalitis admitted to the Neuropediatrics Department of a University Hospital in the period between May 2009 and May 2016 was conducted. Results: Diagnosis of anti-NMDAR encephalitis was established in nine patients. Mean age at diagnosis was 9.4 years and five patients were male. Most cases (88.9%) presented with neuropsychiatric symptomatology. Movement disorders were another frequent finding (88.9%) and include chorea, dystonia and dyskinesias. Altered level of consciousness occurred in 77.8% of cases, insomnia and speech disturbance in 66.7%, seizures in 55.6% and autonomic dysfunction in 22.2%. Anti-NMDAR antibodies were identified in the cerebrospinal fluid of all patients. One patient had an underlying neoplasm. All patients underwent immunosuppressive therapy and seven patients fully recovered. In the remaining patients, sequelae included refractory epilepsy and cognitive impairment. Discussion: The diagnosis of anti-NMDAR encephalitis should be considered in children and adolescents presenting with psychiatric symptoms associated and movement disorders. In this sample, although most patients responded very favorably to treatment, severe sequelae were also observed. This highlights the importance of an early diagnosis to initiate treatment as soon as possible.
publishDate 2019
dc.date.none.fl_str_mv 2019-07-18T00:00:00Z
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dc.identifier.uri.fl_str_mv https://doi.org/10.25753/BirthGrowthMJ.v28.i2.14322
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dc.publisher.none.fl_str_mv Centro Hospitalar Universitário do Porto
publisher.none.fl_str_mv Centro Hospitalar Universitário do Porto
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