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

      case-report

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          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.

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          Most cited references5

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          Idiopathic eosinophilic myositis.

          Eosinophilic myositis is a rare entity accompanying parasitic infection or other inflammatory disorders. Two cases are reported in which myalgia and eosinophilic infiltration of muscle occurred in the absence of associated disease, and twelve previously published cases of idiopathic eosinophilic myositis are reviewed. A classification system for idiopathic eosinophilic muscle disease is proposed, describing three distinct groups. Comparisons are drawn between these and other causes of eosinophilic muscle disease, outlining the differential diagnoses for each group.
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            Polymyositis after propylthiouracil treatment for hyperthyroidism.

            An additional disorder in the spectrum of thyroid related muscle disease is presented. Hypothyroid and hyperthyroid disease are both associated with a variety of muscle abnormalities, from myalgias to myopathy. Polymyositis, however, has never been reported immediately after treatment for active hyperthyroidism. A patient is presented with typical hyperthyroidism, who developed a severe proximal muscle weakness and a raised creatine phosphokinase after treatment for hyperthyroidism with propylthiouracil (100 mg orally, three times a day). Electromyography, muscle biopsy, and the course of the patient's illness were consistent with polymyositis. Whether this represents a cause-effect association or a chance occurrence is unknown. Physician awareness of the occurrence of a variety of muscle disorders including polymyositis in thyroid disease is emphasised. A brief discussion of thyroid myopathy, thionamide drug reactions, and polymyositis is included.
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              Eosinophilic major basic protein and interleukin-5 in eosinophilic myositis.

              To determine whether eosinophils play a critical role in muscle fiber damage in patients with eosinophilic myositis (EM). We investigated expression of eosinophilic major basic protein (MBP) and interleukin (IL)-5 at the protein and mRNA levels in muscle biopsies from three patients with idiopathic EM. MBP deposits were found on the surface of eosinophils and muscle fibers surrounded by the eosinophils. Reverse transcriptase-polymerase chain reaction analysis showed increased IL-5 expression in EM muscle but not in control muscle. These results suggest that IL-5 induces local accumulation of eosinophils and their release of MBP. The secreted proteins adhere to the muscle fiber membrane, resulting in muscle damage.

                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                edm
                EDM Case Reports
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                30 August 2013
                2013
                : 2013
                : 130008
                Affiliations
                [1 ]Department of Endocrinology Saint Georges University Medical Center, University of Balamand BeirutLebanon
                [2 ]Department of Family Medicine Saint Georges University Medical Center, University of Balamand BeirutLebanon
                [3 ]Department of Infectious Diseases Saint Georges University Medical Center, University of Balamand BeirutLebanon
                [4 ]Department of General Surgery Saint Georges University Medical Center, University of Balamand BeirutLebanon
                [5 ]Department of Pathology Saint Georges University Medical Center, University of Balamand BeirutLebanon
                [6 ]Department of Gastroenterology Saint Georges University Medical Center, University of Balamand BeirutLebanon
                Author notes
                Correspondence should be addressed to S Farhat Email: saidfarhat@ 123456hotmail.com
                Article
                EDM130008
                10.1530/EDM-13-0008
                3921996
                9022024b-ecd8-402a-ae7e-2785ff8be1df
                © 2013 The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.

                History
                : 20 July 2013
                : 24 July 2013
                Categories
                Unusual Effects of Medical Treatment

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