TABLE 2.
Patients | 165 |
Chronic fibrosing hypersensitivity pneumonitis | 14 (8.5) |
Idiopathic interstitial pneumonia | 12 (7.3) |
Unclassifiable ILD | 52 (31.5) |
Interstitial pneumonitis with autoimmune features | 2 (1.2) |
Autoimmune ILD | 77 (46.7) |
Rheumatoid arthritis-ILD | 7 (4.2) |
Systemic sclerosis-ILD | 43 (26.1) |
Dermatomyositis-ILD | 12 (7.3) |
Mixed connective tissue disease-ILD | 10 (6.1) |
Other autoimmune ILD# | 5 (3.0) |
Other ILDs¶ | 10 (6.1) |
Data are presented as n or n (%). ILD: interstitial lung disease. #: Sjögren syndrome ILD (n=1), systemic lupus erythematosus (n=1), others (n=3); ¶: exposure-related ILD (n=2), other fibrosing ILD (n=5), sarcoidosis (n=3).