Table 5.
SLB Histopathologic Interpretation | MDD Consensus Clinical Diagnosis | n |
---|---|---|
Usual interstitial pneumonia (UIP) (n = 12) |
Idiopathic pulmonary fibrosis (IPF) | 4 |
Medication-induced ILD | 2 | |
Autoimmune-related ILD | 1 | |
Chronic hypersensitivity pneumonitis (HP) | 1 | |
Occupation-related ILD | 1 | |
Unclassifiable ILD * | 3 | |
Nonspecific interstitial pneumonia (NSIP) (n = 12) |
Chronic hypersensitivity pneumonitis (HP) | 5 |
Autoimmune-related ILD | 3 | |
Idiopathic pulmonary fibrosis (IPF) | 1 | |
Acute interstitial pneumonia (AIP) | 1 | |
Idiopathic NSIP | 1 | |
Unclassifiable ILD * | 1 | |
Unclassifiable fibrosis † (n = 9) |
Smoking-related ILD | 5 |
Chronic hypersensitivity pneumonitis (HP) | 1 | |
Unclassifiable ILD * | 3 | |
Organizing pneumonia (OP) (n = 4) |
Autoimmune-related ILD | 4 |
Hypersensitivity pneumonitis (n = 4) |
Chronic hypersensitivity pneumonitis (HP) | 4 |
unclassifiable ILD indicates two or more ILD diagnoses remained under consideration or ILD remained unclassifiable.
unclassifiable fibrosis indicates histologic findings of pulmonary fibrosis were present, but more specific histopathologic patterns of fibrosis were absent.