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Successful treatment with dimethyl fumarate in a child with relapsing-remitting multiple sclerosis.
Saijo, Naoya; Abe, Yu; Oikawa, Yoshitsugu; Okubo, Yukimune; Endo, Wakaba; Numata-Uematsu, Yurika; Takahashi, Toshiyuki; Uematsu, Mitsugu.
Afiliación
  • Saijo N; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Abe Y; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Oikawa Y; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Okubo Y; Department of Pediatric Neurology, Miyagi Children's Hospital, Sendai, Japan.
  • Endo W; Department of Pediatric Neurology, Miyagi Children's Hospital, Sendai, Japan.
  • Numata-Uematsu Y; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Takahashi T; Department of Neurology, Tohoku University Graduate School of Medicine, Sendai, Japan; Department of Neurology, National Hospital Organization National Yonezawa Hospital, Yonezawa, Japan.
  • Uematsu M; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan. Electronic address: uematsu@bk9.so-net.ne.jp.
Brain Dev ; 44(5): 353-356, 2022 May.
Article en En | MEDLINE | ID: mdl-35058083
INTRODUCTION: Early disease control with disease-modifying drugs is important for improving the prognosis of multiple sclerosis (MS) in children. Dimethyl fumarate (DMF) is an oral disease-modifying drug for MS in adults with relatively stable disease; however, its use in young children has not been heavily documented in the current literature. We report the case of a pediatric patient with relapsing-remitting MS who was treated with DMF. CASE REPORT: A 3-year-old boy with a history of common cold symptoms developed unsteadiness and somnolence. Magnetic resonance imaging revealed multiple white matter lesions. Symptoms were recurrent, and DMF was prescribed at 6 years of age due to a relapse episode with oculomotor disability and facial paralysis. However, disease progression continued, and new lesions were noted at age 7; thus, the dose of DMF was increased to 240 mg/day. No relapse has been observed for over three years; sequelae or severe side effects were absent. CONCLUSIONS: DMF may be a useful oral disease-modifying drug for preventing recurrence in young children with MS.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente / Esclerosis Múltiple Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Humans / Male Idioma: En Revista: Brain Dev Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente / Esclerosis Múltiple Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Humans / Male Idioma: En Revista: Brain Dev Año: 2022 Tipo del documento: Article País de afiliación: Japón