Interstitial Lung Disease Associated With the Idiopathic Inflammatory Myopathies What Progress Has Been Made in the Past 35 Years?

被引:371
作者
Connors, Geoffrey R. [1 ]
Christopher-Stine, Lisa [2 ]
Oddis, Chester V. [3 ]
Danoff, Sonye K. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Pulm & Crit Care Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Div Rheumatol, Baltimore, MD 21205 USA
[3] Univ Pittsburgh, Med Ctr, Dept Med, Div Rheumatol, Pittsburgh, PA USA
关键词
TRANSFER-RNA-SYNTHETASE; INCLUSION-BODY MYOSITIS; PULMONARY-FIBROSIS; AMYOPATHIC DERMATOMYOSITIS; RHEUMATOID-ARTHRITIS; CLINICAL-FEATURES; RISK-FACTORS; CORTICOSTEROID-RESISTANT; MYCOPHENOLATE-MOFETIL; JAPANESE PATIENTS;
D O I
10.1378/chest.10-0180
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Interstitial lung disease is commonly associated with the autoimmune inflammatory myopathies dermatomyositis and polymyositis and accounts for significant morbidity and mortality m these conditions In the 35 years since the association between inflammatory myopathy and interstitial lung disease was initially described, there has been progress in diagnosing and treating this disorder Nevertheless, there remains much about pathogenesis and therapeutics to be learned This review examines the changes in the understanding of this complex condition, highlighting recent advances and areas deserving of further study CHEST 2010, 138(6) 1464-1474
引用
收藏
页码:1464 / 1474
页数:11
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