Table 3. Histopathological diagnosis of patients undergoing TBCB.
Pathological diagnosis | Case (%) |
---|---|
Definitive pathological diagnosis | |
UIP | 77 (20.6) |
NSIP | 48 (12.9) |
OP | 13 (3.5) |
PAP | 14 (3.8) |
LAM | 10 (2.7) |
Lung cancer | 18 (4.8) |
Pneumonia | 9 (2.4) |
Bullous emphysema | 7 (1.9) |
Sarcoidosis | 6 (1.6) |
Pneumoconiosis | 5 (1.3) |
TB | 4 (1.1) |
DIP | 3 (0.8) |
HP | 3 (0.8) |
RB-ILD | 2 (0.5) |
ACFE | 2 (0.5) |
PCP | 1 (0.3) |
PIE | 1 (0.3) |
LCH | 1 (0.3) |
PAM | 1 (0.3) |
Lipid pneumonia | 1 (0.3) |
PO | 1 (0.3) |
Cryptococcosis | 1 (0.3) |
Giant cell interstitial pneumonia | 1 (0.3) |
IPH | 1 (0.3) |
Aspiration pneumonia | 1 (0.3) |
Congenital cystic adenomatoid malformations | 1 (0.3) |
Pulmonary intravascular large B-cell lymphoma | 1 (0.3) |
Possible pathological diagnosis | |
UIP | 5 (1.3) |
HP | 2 (0.5) |
NSIP | 4 (1.2) |
DIP | 1 (0.3) |
OP | 1 (0.3) |
PAP | 2 (0.5) |
RB-ILD | 1 (0.3) |
TB | 2 (0.5) |
PCP | 1 (0.3) |
Sarcoidosis | 2 (0.5) |
Unknown diagnosis | 119 (31.6) |
UIP, usual interstitial pneumonia; NSIP, non-specific interstitial pneumonia; DIP, desquamative interstitial pneumonia; HP, hypersensitivity pneumonitis; PLAM, pulmonary lymphangiomyomatosis; OP, organizing pneumonia; PAP, pulmonary alveolar proteinosis; PCP, pneumocystis pneumonia; PIE, pulmonary infiltration with eosinophilia; RB-ILD, respiratory bronchiolitis-interstitial lung disease; LCH, langerhans cell histiocytosis; TB, tuberculosis; ACFE, airway-centered fibroelastosis; PAM, pulmonary alveolar microlithiasis; PO, pulmonary ossification; IPH, idiopathic pulmonary hemosiderosis.