Frey R A, Keller F, Michel B A
Rheumaklinik, Universitätsspital, Zürich.
Schweiz Med Wochenschr. 1994 May 21;124(20):852-6.
D-penicillamine has been used in the treatment of rheumatoid arthritis for years. As a rare complication of this treatment the occurrence of myasthenia gravis has been described, the clinical features of this complication being indistinguishable from that of idiopathic myasthenia gravis. Both D-penicillamine induced and idiopathic myasthenia gravis show elevated titers of acetylcholine receptor antibodies and respond to acetylcholinesterase inhibitor treatment. We report on a patient with rheumatoid arthritis who, under treatment with D-penicillamine, developed severe myasthenia gravis which required temporary acetylcholinesterase inhibitor therapy. 8 months after D-penicillamine was discontinued the acetylcholine receptor antibodies had disappeared and the acetylcholinesterase inhibitors could be withdrawn. Clinical findings and possible pathogenetic aspects of D-penicillamine induced myasthenia gravis are discussed.
青霉胺已用于治疗类风湿关节炎多年。作为这种治疗的一种罕见并发症,重症肌无力的发生已有报道,这种并发症的临床特征与特发性重症肌无力难以区分。青霉胺诱发的重症肌无力和特发性重症肌无力均显示乙酰胆碱受体抗体滴度升高,且对乙酰胆碱酯酶抑制剂治疗有反应。我们报告一例类风湿关节炎患者,在接受青霉胺治疗时发生了严重的重症肌无力,需要临时使用乙酰胆碱酯酶抑制剂治疗。停用青霉胺8个月后,乙酰胆碱受体抗体消失,乙酰胆碱酯酶抑制剂可以停用。本文讨论了青霉胺诱发重症肌无力的临床发现及可能的发病机制。