Myositis mimics: how to recognize them

被引:10
|
作者
Hilton-Jones, David [1 ]
机构
[1] John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England
关键词
genetic myopathies; inflammatory infiltrates; muscular dystrophy; myositis; necrotizing myopathy; IDIOPATHIC INFLAMMATORY MYOPATHIES; INCLUSION-BODY MYOSITIS; MUSCULAR-DYSTROPHY; NECROTIZING MYOPATHIES; FEATURES; AUTOANTIBODIES; POLYMYOSITIS; DIAGNOSIS; DISEASE;
D O I
10.1097/BOR.0000000000000101
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review To help clinicians to distinguish between myositis (and other immune-mediated and immunosuppressant-responsive disorders) and its many clinical mimics. Recent findings Increasing experience has shown that findings from conventional investigations, such as muscle biopsy, can be misleading. More specialist investigations, notably autoantibody screening, immunocytochemical techniques, and evolving DNA technologies, are powerful tools but experience is currently largely limited to specialist centres - and even these techniques are open to misinterpretation. Summary Misdiagnosis is hazardous to the patient. Treatable conditions may be missed, or patients subjected inappropriately to potentially toxic drug treatments. Judicious use of clinical skills alone should help reduce these risks.
引用
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页码:663 / 670
页数:8
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