Interstitial Pneumonia with Autoimmune Features

被引：4

作者：

Fischer, Aryeh ^{[1
,2
,3
]}

机构：

[1] Univ Colorado, Sch Med, Div Rheumatol, Anschutz Med Campus,12631 East 17th Ave, Aurora, CO 80045 USA

[2] Univ Colorado, Sch Med, Div Pulm Sci, Anschutz Med Campus,12631 East 17th Ave, Aurora, CO 80045 USA

[3] Univ Colorado, Sch Med, Div Crit Care Med, Anschutz Med Campus,12631 East 17th Ave, Aurora, CO 80045 USA

来源：

CLINICS IN CHEST MEDICINE | 2019年 / 40卷 / 03期

关键词：

Idiopathic interstitial pneumonias; Connective tissue diseases; Interstitial lung disease; Pulmonary fibrosis; CONNECTIVE-TISSUE DISEASE; IDIOPATHIC PULMONARY-FIBROSIS; LUNG-DISEASE; SURVIVAL; PREDICTORS; DIAGNOSIS; SERIES; CALL;

D O I：

10.1016/j.ccm.2019.05.007

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

The European Respiratory Society/American Thoracic Society Task Force on Undifferentiated Forms of Connective Tissue Disease-associated Interstitial Lung Disease put forth the research classification interstitial pneumonia with autoimmune features as a step toward uniformly describing these patients. Diverse nomenclature and classification schemes had been proposed to characterize them. This classification has provided uniform nomenclature and criteria, fostering interdisciplinary engagement and research. Longitudinal surveillance is needed; some patients evolve to a defined connective tissue disease. This review discusses cohort studies of interstitial pneumonia with autoimmune features and what they have taught us about the phenotype, and offers insights into future directions.

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页码：609 / +

页数：9

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