Table 2. Final diagnoses of study subjects.
Diagnosis | Number (percentage) |
---|---|
Sarcoidosis | 339 (42.2) |
Stage 0 | 17 (5.0) |
Stage I | 96 (28.3) |
Stage II | 138 (40.7) |
Stage III | 77 (22.7) |
Stage IV | 11 (3.2) |
Idiopathic pulmonary fibrosis (IPF) | 170 (21.2) |
Non-IPF idiopathic interstitial pneumonia | 74 (9.2) |
Nonspecific interstitial pneumonia | 63 (7.8) |
Acute Interstitial Pneumonia | 2 (0.2) |
Cryptogenic Organizing Pneumonia | 4 (0.5) |
Respiratory Bronchiolitis-ILD/Desquamative Interstitial Pneumonia | 5 (0.6) |
Connective tissue disease associated ILD | 102 (12.7) |
Rheumatoid arthritis | 22 (2.7) |
Systemic sclerosis | 19 (2.3) |
Mixed connective tissue disease | 4 (0.5) |
Sjogren’s syndrome | 3 (0.4) |
Systemic lupus erythematosus | 3 (0.4) |
Dermatomyositis/Anti-synthetase syndrome | 6 (0.7) |
Interstitial pneumonia with autoimmune features | 45 (5.6) |
Hypersensitivity pneumonitis | 86 (10.7) |
Farmer’s lung | 51 (6.4) |
Bird fancier’s lung | 13 (1.6) |
Miller’s lung | 3 (0.4) |
Other exposures | 2 (0.2) |
Unknown exposure | 17 (2.1) |
Drug-induced ILD | 6 (0.7) |
Bleomycin | 4 (0.5) |
Methotrexate | 2 (0.3) |
Occupational lung disease | 7 (0.9) |
Arc welder’s lung | 1 (0.1) |
Metal worker’s lung | 1 (0.1) |
Silicosis | 4 (0.5) |
Pneumoconiosis, NOS | 1 (0.1) |
Unclassifiable | 7 (0.9) |
Others | 12 (1.5) |
Chronic eosinophilic pneumonia | 2 (0.2) |
Cystic lung disease, NOS | 1 (0.1) |
CVID associated LIP | 1 (0.1) |
IgG4 associated fibrosis | 2 (0.2) |
Pulmonary alveolar microlithiasis | 1 (0.1) |
Pulmonary alveolar proteinosis | 2 (0.2) |
Lymphangiolieomyomatosis | 1 (0.1) |
Idiopathic pulmonary hemosiderosis | 1 (0.1) |
Pulmonary Langerhan’s cell histiocytosis | 1 (0.1) |
CVID-common variable immunodeficiency, ILD-interstitial lung disease, LIP-lymphocytic interstitial pneumonia, NOS-not otherwise specified.