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首页> 外文期刊>European Journal of Case Reports in Internal Medicine >Inclusion Body Myositis Treated with Alemtuzumab
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Inclusion Body Myositis Treated with Alemtuzumab

机译:阿仑单抗治疗包涵体肌炎

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摘要

Inclusion body myositis (IBM) is a chronic inflammatory myopathy with a progressive course. It is more common in the later years of life and usually presents with limb weakness. We present the case of a patient who developed proximal weakness in the lower limbs and, four years later, facial asymmetry. Blood analysis revealed high lactate dehydrogenase and creatinine kinase values. The diagnosis was obtained through muscle biopsy which met the histological criteria for IBM. The patient started treatment with alemtuzumab, leading to stabilisation of the symptoms in two years.
机译:包涵体肌炎(IBM)是一种慢性炎症性肌病,具有进行性病程。在生命的晚年更常见,通常表现为四肢无力。我们介绍了一名患者,患者下肢近端无力,四年后面部不对称。血液分析显示乳酸脱氢酶和肌酐激酶值较高。诊断是通过符合IBM组织学标准的肌肉活检获得的。患者开始用阿仑单抗治疗,导致症状在两年内稳定下来。

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