Skip to main content
. 2018 Feb 8;13(2):e0191938. doi: 10.1371/journal.pone.0191938

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.