A rare cause of impaired general condition: Muscular and cardiac toxicity of antimalarials

被引:4
作者
Lenfant, T. [1 ]
Dion, J. [1 ]
Maisonobe, T. [2 ]
Costedoat-Chalumeau, N. [1 ]
机构
[1] Hop Cochin, AP HP, Ctr Reference Malad Autoimmunes & Syst Rares, Serv Med Interne Pole Med, 27 Rue Faubourg St Jacques, Paris 75679 14, France
[2] CHU Pitie Salpetriere, Dept Neuropathol, Neurophysiol Clin, 47-83 Blvd Hop, Paris 75651 13, France
来源
REVUE DE MEDECINE INTERNE | 2020年 / 41卷 / 05期
关键词
Cutaneous Lupus; Hydroxychloroquine; Chloroquine; Cardiac Conduction Disorder; Myopathy; Cardiomyopathy; INDUCED CARDIOMYOPATHY; CHLOROQUINE CARDIOMYOPATHY; LUPUS; CARDIOTOXICITY; DIAGNOSIS;
D O I
10.1016/j.revmed.2020.04.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction. - This case report signifies the need to systemically assess antimalarial toxicity in those undergoing long-term treatment. Case report. - A 59-year-old man with a history of ischemic-labeled heart disease revealed by conduction disorders and cutaneous lupus treated initially with hydroxychloroquine followed by chloroquine consulted for asthenia and weight loss. Clinically, he had a muscular atrophy, a motor deficit, and an abolition of the osteo-tendinous reflexes in the lower limbs. Adverse drug effects of the antimalarial therapy were suspected-specifically, muscular and cardiac toxicity. The diagnosis was confirmed with a muscle biopsy, which showed typical and florid vacuolar myopathy. Cessation of the drug resulted in a slow regression of symptoms. Conclusion. - Cardiac and muscular toxicity related to antimalarials are rare and sometimes fatal; thus, they must be systematically assessed in a patient with several years of exposure. A muscle biopsy could be sufficient to allow for the diagnosis. (C) 2020 Societe Nationale Francaise de Medecine Interne (SNFMI). Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:335 / 338
页数:4
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