D-penicillamine Induced Myasthenia Gravis
نویسندگان
چکیده
Rheumatoid arthritis can be a very mutilating disease and, as a result, the likelihood of patients with rheumatoid arthritis requiring surgery and anaesthesia is increased. D-penicillamine (D-Pen) has been used in the treatment of rheumatoid arthritis and Wilson's disease since the early 1960s. Its true mode of action is unknown, but it appears to modify the immune response. Treatment with D-Pen is associated with many side effects, one of which is the induction of several conditions of which autoantibody production is a feature; for example, systemic lupus erythematosus, pemphigus, Goodpasture's syndrome, polymyositis, autoimmune thyroiditis and myasthenia gravis (Bucknall et al., 1975; Bucknall, 1977; Gordon and Burnside, 1977). A variety of auto-antibodies may be detected following the administration of D-Pen: anti-nuclear factor, anti-striational antibodies and anti-acetylcholine receptor antibodies (Masters et al., 1977; Russel and Lindstrom, 1978; Vincent, Newsom-Davis and Martin, 1978).
منابع مشابه
D-Penicillamine induced myasthenia gravis.
Myasthenia gravis is a disorder of impaired neuromuscular transmission resulting in weakness and abnormal fatigability on exertion, improved by anti-acetyl cholinesterase drugs. A number of drugs are known to exacerbate myasthenia gravis or interfere with neuromuscular transmission. We report a case of D-penicillamine induced myasthenia gravis who developed ptosis, diplopia and easy fatigabilit...
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The case of a 57-year-old woman with rheumatoid arthritis is presented to illustrate the rare occurrence of a myasthenic syndrome induced by D-penicillamine, which led to prolonged (5.25-h) postoperative apnoea necessitating artificial ventilation.
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Antibodies to the acetylcholine receptor and HLA antigens have been studied in patients with myasthenia gravis occurring in association with penicillamine treatment. The properties of the antiacetylcholine receptor in these patients differed from those in patients with idiopathic myasthenia gravis in terms of specificity and affinity. These patients had an increased prevalence of HLA Bw35 and D...
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A 68-year-old black woman who was put on D-penicillamine therapy (250-500 mg per day, total dose 15 g) for rheumatoid arthritis developed ocular myasthenia gravis. Two weeks after she discontinued D-penicillamine her signs and symptoms cleared with no other treatment. Review of previous cases and possible immunological mechanisms are discussed.
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