Connective Tissue Related Interstitial Lung Disease

被引:0
|
作者
Gadre, Abhishek [1 ]
Highland, Kristin B. [2 ]
机构
[1] Univ Calif San Diego, Div Pulm & Crit Care Med, La Jolla, CA 92093 USA
[2] Cleveland Clin Fdn, Resp Inst, 9500 Euclid Ave,A90, Cleveland, OH 44195 USA
关键词
Interstitial lung disease; IPAF; Scleroderma; Dermatomyositis; Polymyositis; Rheumatoid arthritis; Sjogren's syndrome; Systemic lupus erythematosus;
D O I
10.1007/s13665-018-0212-5
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose of ReviewInterstitial lung disease (ILD) is a common complication of the connective tissue diseases (CTD) and results in significant morbidity and mortality. This review will focus on recent literature pertaining to the epidemiology, clinical presentation, diagnosis, and treatment of CTD-ILD.Recent FindingsSubclinical ILD can be found in the majority of patients with CTD. Clinically significant ILD is most commonly seen in scleroderma followed by polymyositis/dermatomyositis and rheumatoid arthritis, although it can occur in all of the CTDs. Nonspecific interstitial pneumonia is the most common radiographic and histologic pattern, although usual interstitial pneumonia occurs more frequently in rheumatoid arthritis. Pathogenesis is likely related to a combination of autoimmunity/inflammation, disordered fibrogenesis, and vascular injury. Treatment strategies are evolving to target all three of these pathways.SummaryAlthough further research into treatment strategies is needed, the clinician should be aware of the risk factors and clinical presentation of ILD in the various CTDs in order to identify patients who should be screened and/or have modifications in treatment strategies in order to mitigate the morbidity and mortality associated with CTD-ILD.
引用
收藏
页码:133 / 148
页数:16
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