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[类风湿关节炎中D-青霉胺诱发的肌无力综合征。两例报告(作者译)]

[D-penicillamine induced myasthenic syndromes in rheumatoid arthritis. Two cases (author's transl)].

作者信息

Rodat O, Hamelin J P, Rossard A, Cottin S, Cler J M, Rodat G, Lemouroux P

出版信息

Nouv Presse Med. 1981 May 2;10(20):1645-8.

PMID:7255126
Abstract

The authors report on 2 personal cases, and review 48 published cases of myasthenia induced by D-penicillamine (D-P) treatment in patients with rheumatoid arthritis. The clinical symptoms were not different from those of myasthenia gravis, and no correlation could be found between the total cumulative dose of D-P and the onset on the myasthenic syndrome. In 71% of the patients the neurological deficiency regressed after D-P was withdrawn, but in some cases anticholinesterase treatment had to be continued and thymectomy was contemplated. The most remarkable biological abnormalities were anti-striational antibodies (found in 58% of the cases) and anti-acetylcholine receptors antibodies (found in 4 out of 7 patients tested). These findings are in favour of a genuine myasthenia and against a myasthenic syndrome due to neuro-muscular blockade. While the mechanisms underlying the emergence of these antibodies remains unknown, their presence throws new light on immunological disorders in rheumatoid arthritis.

摘要

作者报告了2例个人病例,并回顾了48例已发表的类风湿关节炎患者因使用青霉胺(D-P)治疗而诱发重症肌无力的病例。临床症状与重症肌无力无异,且未发现D-P的累计总剂量与肌无力综合征的发病之间存在关联。71%的患者在停用D-P后神经功能缺损有所恢复,但在某些情况下,必须继续进行抗胆碱酯酶治疗并考虑胸腺切除术。最显著的生物学异常是抗横纹肌抗体(58%的病例中发现)和抗乙酰胆碱受体抗体(7例检测患者中有4例发现)。这些发现支持真性重症肌无力,而非神经肌肉阻滞所致的肌无力综合征。虽然这些抗体出现的潜在机制尚不清楚,但它们的存在为类风湿关节炎的免疫紊乱提供了新的线索。

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