イディオパシー性炎症性ミオパシーの臨床表現,病原性,治療の解読
Lisa G Rider1, Frederick W Miller
1Environmental Autoimmunity Group, Program of Clinical Research, National Institute of Environmental Health Sciences, National Institutes of Health, US Department of Health and Human Services, Bethesda, Maryland 20892, USA. riderl@mail.nih.gov
JAMA
|January 13, 2011
まとめ
ポリミオサイトと皮膚ミオサイトを含むイディオパシー性炎症性ミオパシーは,筋肉の弱さを引き起こす自己免疫疾患です. これらの筋炎症症候群を異なる現象型に分類することは,患者のアウトカムを予測し,治療戦略を導くのに役立ちます.
科学分野:
- レウマトロジーの病理学
- 免疫学 免疫学とは
- 神経学 神経学とは
背景:
- イディオパシー炎症性ミオパシー (Idiopathic inflammatory myopathies,IIMs) は,慢性的な筋肉の弱さと炎症によって特徴づけられる全身性自己免疫疾患である.
- 一般的な形態には,ポリミオサイト,皮膚ミオサイト,インクルージョンボディミオサイトなどがあり,著しい罹病率と死亡率をもたらします.
- IIMの病因はほとんど不明のままである.
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