TY - JOUR
T1 - Successful treatment with dimethyl fumarate in a child with relapsing-remitting multiple sclerosis
AU - Saijo, Naoya
AU - Abe, Yu
AU - Oikawa, Yoshitsugu
AU - Okubo, Yukimune
AU - Endo, Wakaba
AU - Numata-Uematsu, Yurika
AU - Takahashi, Toshiyuki
AU - Uematsu, Mitsugu
N1 - Funding Information:
No grant was provided for this analysis and this study.
Publisher Copyright:
© 2022 The Japanese Society of Child Neurology
PY - 2022/5
Y1 - 2022/5
N2 - 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.
AB - 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.
KW - Dimethyl fumarate
KW - Multiple sclerosis
KW - Pediatric
KW - Relapsing-remitting
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U2 - 10.1016/j.braindev.2021.12.010
DO - 10.1016/j.braindev.2021.12.010
M3 - Article
C2 - 35058083
AN - SCOPUS:85123075422
SN - 0387-7604
VL - 44
SP - 353
EP - 356
JO - Brain and Development
JF - Brain and Development
IS - 5
ER -