Abstract
Muscle-specific kinase (MuSK) myasthenia gravis (MG) is relatively rare and has a higher incidence of myasthenic crisis compared with other subtypes. However, there is still a lack of effective treatment for refractory MuSK MG. We report the case of a 70-year-old female MuSK MG patient with recurrent fluctuations who stabilized on telitacicept in combination with anti-CD20 B-cell depletion therapy. This combination regimen deserves further investigation. Furthermore, we summarized the treatment protocols of 14 previously reported cases of MuSK MG.
Keywords:
B-cell depletion therapy; case report; muscle-specific tyrosine kinase; myasthenia gravis; telitacicept.
Copyright © 2024 Wang, Zheng, Wei, Wu, Feng, Chen, Liu, Qin, Qin and Kong.
MeSH terms
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Aged
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Autoantibodies* / blood
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Autoantibodies* / immunology
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B-Lymphocytes* / immunology
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Female
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Humans
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Lymphocyte Depletion*
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Myasthenia Gravis* / diagnosis
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Myasthenia Gravis* / drug therapy
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Myasthenia Gravis* / immunology
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Myasthenia Gravis* / therapy
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Receptor Protein-Tyrosine Kinases* / immunology
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Receptors, Cholinergic* / immunology
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Rituximab / therapeutic use
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Treatment Outcome
Substances
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MUSK protein, human
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Receptors, Cholinergic
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Receptor Protein-Tyrosine Kinases
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Autoantibodies
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Rituximab
Grants and funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Sanming Project of Medicine in Shenzhen (grant numbers SZZYSM202111011); Traditional Chinese Medicine Bureau of Guangdong Province (grant numbers 20221357); “3030 project” of Clinical Research Program in Shenzhen Traditional Chinese Medicine Hospital in 2021 (grant numbers G3030202132).