Pediatric Multiple Sclerosis—Experience of a Tertiary Care Center

Cecília Martins; Raquel Samões; Ana Martins Silva; Ernestina Santos; Sónia Figueiroa

doi:10.1055/s-0042-1759843

Neuropediatrics, Inhaltsverzeichnis

Neuropediatrics 2023; 54(01): 058-063
DOI: 10.1055/s-0042-1759843

Original Article

Pediatric Multiple Sclerosis—Experience of a Tertiary Care Center

Cecília Martins

¹Department of Pediatrics, Centro Hospitalar do Médio Ave, V. N. Famalicão, Portugal

²Department of Pediatric Neurology, Centro Materno Infantil do Norte/Centro Hospitalar Universitário do Porto, Porto, Portugal

,

Raquel Samões

³Department of Neurology, Hospital Santo António/Centro Hospitalar Universitário do Porto, Porto, Portugal

⁴Multidisciplinary Unit for Biomedical Research, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal

,

Ana Martins Silva

³Department of Neurology, Hospital Santo António/Centro Hospitalar Universitário do Porto, Porto, Portugal

⁴Multidisciplinary Unit for Biomedical Research, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal

,

Ernestina Santos

³Department of Neurology, Hospital Santo António/Centro Hospitalar Universitário do Porto, Porto, Portugal

⁴Multidisciplinary Unit for Biomedical Research, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal

,

Sónia Figueiroa

²Department of Pediatric Neurology, Centro Materno Infantil do Norte/Centro Hospitalar Universitário do Porto, Porto, Portugal

› Institutsangaben

Abstract

Background Pediatric-onset multiple sclerosis (POMS) accounts for 3 to 10% of all MS diagnoses. POMS is usually characterized by prominent disease activity, and patients are at higher risk of developing physical disability and cognitive impairment.

Objective This article characterizes a cohort of POMS patients followed at the pediatric neurology unit of a Portuguese tertiary hospital.

Methods Retrospective observational study. Clinical records of all patients with POMS between 2011 and 2020 were revised.

Results A total of 21 patients, with a female:male ratio of 11:10 and a mean age of onset of 14.8 years were included. Clinical manifestations at presentation included myelitis in eight patients (two with associated brainstem syndrome), optic neuritis in six (one with associated cerebellar syndrome), supratentorial symptoms in four, and isolated brainstem syndrome in two. Twenty patients had oligoclonal immunoglobulin G bands in cerebrospinal fluid. Supra- and infratentorial involvement was identified in the first brain magnetic resonance imaging of nine patients. Initial relapses were treated with intravenous steroids in 19 patients. The mean time for diagnosis was 2.8 months. Eleven patients were on first-line treatment (nine on β-interferon, two on teriflunomide) and 10 on second-line treatment (six on natalizumab, three on fingolimod, one on ocrelizumab). The mean annual relapse rate was 0.29 (range, 0.01–3), and the median Expanded Disability Status Scale was 1. Four patients reported learning disabilities and/or cognitive deficits.

Conclusion About half of patients in this cohort were on second-line disease-modifying treatment, with 19% showing cognitive impairment. Efforts to establish an early diagnosis are crucial to improving these patients' outcomes.

Keywords

adolescence - childhood - multiple sclerosis - neuroimmunology

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Referenzen

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