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Case report: Varicella associated neuropsychiatric syndrome (VANS) in two pediatric cases.
Dahiya, Devika; Matos, Claudia Marques; Lim, Ming; Madureira, Ines; Duarte, Sofia; Byrne, Susan; Rossor, Thomas.
Afiliación
  • Dahiya D; The School of Medicine and Department of Paediatrics, Royal College of Surgeons in Ireland, Department of Paediatric Neurology, Dublin 2, Ireland.
  • Matos CM; Pediatric Neurology Department, Hospital Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, Lisboa, Portugal.
  • Lim M; Children's Neurosciences, Evelina London Children's Hospital at Guy's and St Thomas' NHS Foundation Trust, King's Health Partners Academic Health Science Centre, London, UK.
  • Madureira I; Department Women and Childrens Health, School of Life Course Sciences (SoLCS), Kings College London, UK.
  • Duarte S; Pediatric Rheumatology Unit, Hospital Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, Lisboa, Portugal.
  • Byrne S; Pediatric Neurology Department, Hospital Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, Lisboa, Portugal.
  • Rossor T; The School of Medicine and Department of Paediatrics, Royal College of Surgeons in Ireland, Department of Paediatric Neurology, Dublin 2, Ireland.
Brain Behav Immun Health ; 28: 100602, 2023 Mar.
Article en En | MEDLINE | ID: mdl-36860280
Background: Viral or bacterial infections can trigger auto-immune inflammatory reactions and conditions in children. Self-reactivity arises due to similarities in molecular structures between pathogenic microorganisms and regular body structures with consequent immune-cross reactions. Reactivation of latent Varicella Zoster Virus (VZV) infections can cause neurological sequalae, including cerebellitis, post-herpetic neuralgias, meningo/encephalitis, vasculopathy and myelopathy. We propose a syndrome caused by auto-immune reactivity triggered by molecular mimicry between VZV and the brain, culminating in a post-infectious psychiatric syndrome with childhood VZV infections. Case presentation: Two individuals, a 6-year-old male and 10-year-old female developed a neuro-psychiatric syndrome 3-6 weeks following a confirmed VZV infection with intrathecal oligoclonal bands. The 6-year-old male presented with a myasthenic syndrome, behavior deterioration and regression in school, he was poorly responsive to IVIG and risperidone, however had a pronounced response to steroid treatment. The 10-year-old female presented with marked insomnia, agitation, and behavioral regression as well as mild bradykinesia. A trial of neuroleptics and sedatives resulted in a mild unsustained reduction in psychomotor agitation and IVIG was also unsuccessful, however the patient was very responsive to steroid therapy. Conclusion: Psychiatric syndromes with evidence of intrathecal inflammation temporally related to VZV infections that are responsive to immune modulation have not been described before. Here we report two cases demonstrating neuro-psychiatric symptoms following VZV infection, with evidence of persistent CNS inflammation following the resolution of infection, and response to immune modulation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Brain Behav Immun Health Año: 2023 Tipo del documento: Article País de afiliación: Irlanda Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Brain Behav Immun Health Año: 2023 Tipo del documento: Article País de afiliación: Irlanda Pais de publicación: Estados Unidos