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[A case of cyclosporin A-induced myopathy].

作者信息

Yamanishi Y, Ishibe Y, Taooka Y, Mukuzono H, Aoi K, Yamana S

机构信息

Immunology and Rheumatology Division, Saijo Central Hospital, Higashi-Hiroshima City.

出版信息

Ryumachi. 1993 Feb;33(1):63-7.

PMID:8493586
Abstract

A 40-year old man with Behçet's disease was admitted for severe decrease of visual acuity. Since 1987, he had suffered from oral aphtha, retinitis, erythema nodosum, genital ulcer and epididymitis. He was diagnosed as complete Behçet's disease and has been administered cyclosporin A (CYA) and colchicine (Col). Because of repeated ocular attacks and reduced visual acuity, CYA was increased from 3.49 mg/kg/day (220 mg/day) to 6.35 mg/kg/day (400 mg/day) and Col, 0.5 mg/day to 1.0 mg/day. 2 weeks later, he revealed fever, generalized myalgia, muscle weakness and general fatigue, accompanying marked elevation of creatine kinase (4962 IU/l). CYA was discontinued and Col was diminished to 0.5 mg/day. The myalgia disappeared in 4 days and general conditions including creatine kinase were normalized within 2 weeks. We concluded that CYA was highly suspected of the cause of myopathy considering his clinical course.

摘要

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Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and Amiodarone.糖原贮积症VII型患者出现晚期严重肌病,环孢素和胺碘酮使其病情恶化
Front Neurol. 2019 Feb 7;10:77. doi: 10.3389/fneur.2019.00077. eCollection 2019.