Methimazole-induced myositis: a case report and review of the literature

Summary Methimazole is an anti-thyroid drug commonly used to treat hyperthyroidism and is a relatively safe medication. Several side effects have been reported and usually develop within 3 months of therapy. Well-known adverse reactions include agranulocytosis, hepatitis, skin eruptions, and musculo...

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Veröffentlicht in:Endocrinology, diabetes & metabolism case reports diabetes & metabolism case reports, 2013-08, Vol.2013, p.130008-130008
Hauptverfasser: Bou Khalil, R, Abou Salbi, M, Sissi, S, El Kara, N, Azar, E, Khoury, M, Abdallah, G, Hreiki, J, Farhat, S
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Sprache:eng
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Zusammenfassung:Summary Methimazole is an anti-thyroid drug commonly used to treat hyperthyroidism and is a relatively safe medication. Several side effects have been reported and usually develop within 3 months of therapy. Well-known adverse reactions include agranulocytosis, hepatitis, skin eruptions, and musculoskeletal complaints such as myalgia, arthralgia, and arthritis. So far, myositis secondary to carbimazole was described in the context of a lupus-like syndrome or other rare cases of anti-neutrophil cytoplasmic antibodies-associated vasculitis. Methimazole-induced myositis occurring independently of such reactions was rarely stated. We report a patient with hyperthyroidism who, early after therapy with methimazole, developed hepatitis, eosinophilia, and fever that resolved completely after stopping the medication as well as a delayed onset of biopsy-proven eosinophilic myositis and fasciitis of gluteal muscles that resolved eventually without any additional therapy. Therefore, we raise the awareness regarding a rare side effect of methimazole: myositis. Learning points Several differential diagnoses arise when managing a hyperthyroid patient with muscle complaints. Both hyperthyroidism and methimazole are associated with myositis. Methimazole-induced myositis is a rare clinical entity. Resolution of symptoms may occur after stopping methimazole.
ISSN:2052-0573
2052-0573
DOI:10.1530/EDM-13-0008