Mastaglia F L, Zilko P J
Centre for Neuromuscular and Neurological Disorders, and Department of Medicine, University of Western Australia, Nedlands, WA, Australia.
J Clin Neurosci. 2003 Jan;10(1):99-101. doi: 10.1016/s0967-5868(02)00271-0.
The initial approach to the treatment of patients with inflammatory myopathy is critical in determining the subsequent course and outcome. Prolonged administration of high doses of corticosteroids should be avoided and a second-line agent such as methotrexate or azathioprine should be introduced earlier rather than later. Intravenous immunoglobulin therapy has an important place if the myositis remains active, particularly in patients with dermatomyositis, and is the treatment of choice in patients with immunodeficiency who are not controlled by corticosteroids. In more resistant cases of polymyositis or dermatomyositis it may be necessary to use cyclophosphamide, cyclosporin or the promising newer immunosuppressive agents mycophenolate mofetil or tacrolimus to achieve disease control. The treatment of inclusion body myositis remains unsatisfactory but a trial of prednisolone and methotrexate is warranted in selected patients.
炎症性肌病患者的初始治疗方法对于决定后续病程和预后至关重要。应避免长期大剂量使用糖皮质激素,应尽早而非推迟引入二线药物,如甲氨蝶呤或硫唑嘌呤。如果肌炎持续活动,静脉注射免疫球蛋白疗法具有重要地位,尤其对于皮肌炎患者,并且是糖皮质激素无法控制的免疫缺陷患者的首选治疗方法。在多肌炎或皮肌炎更具耐药性的病例中,可能有必要使用环磷酰胺、环孢素或有前景的新型免疫抑制剂霉酚酸酯或他克莫司来控制病情。包涵体肌炎的治疗仍不尽人意,但对于部分患者,泼尼松龙和甲氨蝶呤试验是有必要的。