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

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 en...

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Main Authors: Mariana Amorim Branco, Luísa Sousa, Cristina Garrido, Inês Carrilho, Manuela Santos, Teresa Temudo, Ana Martins Silva, Sónia Figueiroa
Format: Article
Language:English
Published: Centro Hospitalar do Porto 2019-07-01
Series:Nascer e Crescer
Subjects:
Online Access:https://revistas.rcaap.pt/nascercrescer/article/view/14322
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spelling doaj-a50ac56e31614342a58b010710015faf2020-11-25T01:11:35ZengCentro Hospitalar do PortoNascer e Crescer 2183-94172019-07-01282636910.25753/BirthGrowthMJ.v28.i2.1432214322Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric ageMariana Amorim Branco0Luísa Sousa1Cristina Garrido2Inês Carrilho3Manuela Santos4Teresa Temudo5Ana Martins Silva6Sónia Figueiroa7Neuropediatrics Department, Centro Materno-Infantil do Norte, Centro Hospitalar Universitário do PortoNeurology Department, Centro Hospitalar Universitário do PortoNeuropediatrics Department, Centro Materno-Infantil do Norte, Centro Hospitalar Universitário do PortoNeuropediatrics Department, Centro Materno-Infantil do Norte, Centro Hospitalar Universitário do PortoNeuropediatrics Department, Centro Materno-Infantil do Norte, Centro Hospitalar Universitário do PortoNeuropediatrics Department, Centro Materno-Infantil do Norte, Centro Hospitalar Universitário do PortoNeurology Department, Centro Hospitalar Universitário do PortoNeuropediatrics Department, Centro Materno-Infantil do Norte, Centro Hospitalar Universitário do PortoIntroduction: 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.https://revistas.rcaap.pt/nascercrescer/article/view/14322antibodiesencephalitisneoplasm
collection DOAJ
language English
format Article
sources DOAJ
author Mariana Amorim Branco
Luísa Sousa
Cristina Garrido
Inês Carrilho
Manuela Santos
Teresa Temudo
Ana Martins Silva
Sónia Figueiroa
spellingShingle Mariana Amorim Branco
Luísa Sousa
Cristina Garrido
Inês Carrilho
Manuela Santos
Teresa Temudo
Ana Martins Silva
Sónia Figueiroa
Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
Nascer e Crescer
antibodies
encephalitis
neoplasm
author_facet Mariana Amorim Branco
Luísa Sousa
Cristina Garrido
Inês Carrilho
Manuela Santos
Teresa Temudo
Ana Martins Silva
Sónia Figueiroa
author_sort Mariana Amorim Branco
title Anti-N-Methy-D-Aspartate receptor encephalitis in pediatric age
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
publisher Centro Hospitalar do Porto
series Nascer e Crescer
issn 2183-9417
publishDate 2019-07-01
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.
topic antibodies
encephalitis
neoplasm
url https://revistas.rcaap.pt/nascercrescer/article/view/14322
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