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. 2012 May 22:165–176. doi: 10.1007/978-1-4614-4292-9_16

Table 16.1.

Diagnosis and BAL

Diagnosis BAL features
Alveolar hemorrhage Macroscopically bloody
Increased intensity from fraction to fraction
Free red blood cells
Hemosiderin-laden macrophages
Fragmented red blood cells in the alveolar macrophages
≥20% siderophages
Alveolar proteinosis Milky fluid, PAS  +  acellular corpuscles
Foamy alveolar macrophages
Large amounts of amorphous debris, weak PAS+
Cigarette smoking Three- to fivefold increase of size of alveolar macrophages
Inclusion bodies (cytoplasmic inclusion of tar products, lipids, lipofuscin)
Eosinophilic pneumonia Eosinophils >25%
Hypersensitivity pneumonitis Lymphocytosis >25%
Highest lymphocyte count
CD4/CD8 ratio decreased, but variable too
Infection Infectious organisms by stains or cultures
Langerhans’ cell histiocytosis CD1a  +  or Langerin  +  Langerhans’ cells >5%
Typical smoker’s changings
Lipoid pneumonia Oily material
Lipid-laden alveolar macrophages
Malignant infiltrations Malignant cells
Pneumoconiosis Dust particles in alveolar macrophages
Birefringent material in alveolar macrophages
Asbestosis Increased asbestos body count
Sarcoidosis Lymphocytosis >25%, but milder
Moderate lymphocyte count only
CD4/CD8 ratio >3.5 (in the absence of mixed cellular pattern)