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Baricitinib as a treatment for myasthenia gravis: a case report.
Iguchi, Masahiro; Honjo, Jyunichiro; Yamamoto, Toshiyuki; Kanai, Kazuaki.
Afiliação
  • Iguchi M; Department of Neurology, Fukushima Medical University, 1 Hikarigaoka, Fukushima City, Fukushima, Japan. Electronic address: miguchi-twmu@umin.ac.jp.
  • Honjo J; Department of Ophthalmology Fukushima Medical University, Japan.
  • Yamamoto T; Department of Dermatology, Fukushima Medical University, Japan.
  • Kanai K; Department of Neurology, Fukushima Medical University, 1 Hikarigaoka, Fukushima City, Fukushima, Japan.
Neuromuscul Disord ; 41: 56-58, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38954991
ABSTRACT
Myasthenia gravis (MG) is an autoimmune disease that targets neuromuscular junctions. While immunotherapy remains the cornerstone of treatment, the effects of Janus kinase (JAK) inhibitors on MG remain underexplored. In this report, we describe the case of a 58-year-old woman with ocular myasthenia gravis who received treatment with the JAK inhibitor, baricitinib for alopecia areata. The patient presented with left eyelid ptosis and an inadequate response to steroids and pyridostigmine, along with symptoms of alopecia areata. Following diagnosis, we initiated a treatment regimen consisting of baricitinib for six months. After initiation of baricitinib, we observed a complete resolution of the patient's MG symptoms, accompanied by hair regrowth, even when steroids were tapered and pyridostigmine was discontinued. Furthermore, the titer of the anti-acetylcholine receptor antibody was decreased. This report represents the first reported case of anti-acetylcholine receptor antibody-positive MG that was successfully treated through the inhibition of JAK activity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article