Table 3.
Diagnosis | Histopathological diagnoses (n=46) | Consensus diagnoses (n=71) |
---|---|---|
IPF/UIP | 19 | 22† |
HP | 3 | 8 |
Chronic aspiration | 7 | |
CB | 4 | 4 |
CTD-ILD | 4 | |
NSIP | 2 | 3 |
BO | 3 | 3 |
Sarcoidosis | 2 | 3 |
Malignancy | 2 | 2† |
RB/RB-ILD | 2 | 2 |
OP | 4 | |
due to drug | 2 | |
Cryptogenic | 2† | |
Normal lung / no DPLD | 1 | 2 |
DIP | 1 | 1 |
FB | 1 | 1 |
PAP | 1 | 1 |
Silicosis | 1 | 1 |
Fungal infection | 1 | |
Asbestosis | 1 | |
Drug Pneumonitis | 1 |
Presented as number of diagnoses. IPF = idiopathic pulmonary fibrosis; UIP = usual interstitial pneumonia; HP = hypersensitivity pneumonitis; CB = constrictive bronchiolitis; CTD-ILD = connective tissue disease-related interstitial lung disease; NSIP = nonspecific interstitial pneumonia; BO = bronchiolitis obliterans; RB = respiratory bronchiolitis; OP = organizing pneumonia; DPLD = diffuse parenchymal lung disease; DIP = desquamative interstitial pneumonia; FB = follicular bronchiolitis; PAP = protein alveolar proteinosis;
An additional case, not included in the annotated count, was later diagnosed by surgical lung biopsy.