Treatment of inclusion body myositis: is low-dose intravenous immunoglobulin the solution?

被引:13
|
作者
Recher, Mike [1 ]
Sahrbacher, Ulrike [1 ]
Bremer, Juliane [2 ]
Arndt, Boerge [1 ]
Steiner, Urs [1 ]
Fontana, Adriano [1 ]
机构
[1] Univ Zurich Hosp, Clin Immunol, Dept Internal Med, CH-8044 Zurich, Switzerland
[2] Univ Zurich Hosp, Inst Neuropathol, Dept Pathol, CH-8091 Zurich, Switzerland
关键词
IBM; IVIG; Myositis; Inclusion body myositis; Low-dose IVIG; IDIOPATHIC THROMBOCYTOPENIC PURPURA; ANTIINFLAMMATORY ACTIVITY; INFLAMMATORY MYOPATHIES; GAMMA-GLOBULIN; DOUBLE-BLIND; IVIG; DERMATOMYOSITIS; FC; POLYMYOSITIS; RECEPTOR;
D O I
10.1007/s00296-009-1290-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inclusion body myositis (IBM), the most common inflammatory myopathy in the elderly, is often resistant to various forms of therapy. Placebo-controlled treatment trials with high dose intravenous immunoglobulins (IVIG) have shown disease amelioration in some but not all patients. Here, we present the informative case of a 70-year-old woman with diagnosed inclusion body myositis that showed progressive muscle weakness without treatment and following immuno-suppressive treatment with corticosteroids and azathioprine. A trial with low-dose intravenous immunoglobulins was started at that time. The patient responded rapidly to low dose IVIG treatment with amelioration of muscle strength and normalization of CK serum activities. Our results demonstrate that IBM patients may respond to low-dose IVIG treatment which has important clinical and economic consequences.
引用
收藏
页码:469 / 472
页数:4
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