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. 2017 Sep;9(Suppl 10):S996–S1010. doi: 10.21037/jtd.2017.06.39

Table 2. BAL findings that are highly suggestive of specific types of ILD.

Progressive increase in bloody fluid return with sequential lavages/hemosiderin positive alveolar macrophage °˙ diffuse alveolar hemorrhage
Milky fluid with positive periodic Acid-Schiff staining and amorphous acellular debris °˙ pulmonary alveolar proteinosis
Malignant cells per light microscopy or flow cytometry °˙ cancer
Lymphocytosis (>25%) °˙ granulomatous diseases: sarcoidosis, hypersensitivity pneumonitis, or chronic beryllium disease
Neutrophilia (>50%) °˙ acute lung injury, aspiration pneumonia, or suppurative infection
Eosinophilia (>25%) °˙ virtually diagnostic of acute or chronic eosinophilic pneumonia
A cell differential count of >1% mast cells, >50% lymphocytes, and >3% neutrophils °˙ acute hypersensitivity pneumonitis
A predominance of macrophages containing smoking-related inclusions with no or minor increases in other cell types °˙ smoking-related ILDs (DIP, RBILD, or PLCH)
CD4/CD8 >4 °˙ sarcoidosis
CD1a positive cells ≥5%/Birbeck granules in macrophages (electron microscopy) °˙ Langerhans’ cell histiocytosis
Positive lymphocyte transformation test to specific beryllium antigen °˙ chronic beryllium disease
Ferruginous bodies °˙ asbestosis
Dust particles by polarized microscope °˙ silicosis
Lipid-laden macrophages (oil-red-O-stain) °˙ lipoid pneumonia/chronic microaspiration