Annals of Clinical Neurophysiology
- Volume 4 Issue 1
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- Pages.7-11
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- 2002
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- 2508-691X(pISSN)
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- 2508-6960(eISSN)
Steroid Myopathy
스테로이드 근병증
- Lee, Dong Kuck (Department of Neurology, School of Medicine, Catholic University of Daegu)
- 이동국 (대구가톨릭대학교 의과대학 신경과학교실)
- Published : 2002.05.01
Abstract
Among drug-induced myopathy, steroids are probably the most common cause. The risk of steroid myopathy(SM) increases with the dose and duration of use. It is typically a proximal myopathy, preferentially affecting the hip girdle muscles. Motor and sensory nerve conduction studies are normal. The needle EMG is usually within the normal range or may be minimally abnormal. Occasionally, low-amplitude, short-duration MUAPs may be seen in the proximal muscles. Of note, abnormal spontaneous activity is not seen. This point is often very useful in differentiating polymyositis(PM) from SM. It is common for patients with PM to be treated with steroids, respond well, and then have the steroids tapered. If muscle weakness then returns, it may be very difficult to differentiate recurrent PM from SM on clinical grounds. The presence of abundant abnormal spontaneous activity strongly suggests PM rather than SM.