Lymphocytic |
Hypersensitivity pneumonitis |
Highest numbers of lymphocytes |
Highest cell counts |
Lymphocytosis >50% |
Low CD4/CD8 most common |
Foamy macrophages |
Plasma cells may be present (antigen exposure) and transient neutrophil count |
|
Sarcoidosis |
Mostly isolated moderate lymphocytosis |
Neutrophils and mast cells may be present |
CD4/CD8 ratio >3.5, but high variability |
Consider transbronchial lung biopsy |
Consider EBUS-TBNA |
|
Nonspecific interstitial pneumonia |
Cellular variant |
Higher lymphocyte count |
Lower neutrophil count |
Eosinophils may be present |
|
Cryptogenic organizing pneumonia |
Lymphocytes dominantly increased |
Neutrophils, eosinophils, and mast cells increased |
Typical symptoms and radiological findings |
|
Drug-induced lung disease |
Dominance of CD8+ cells |
|
Silicosis |
Dust particles in alveolar macrophages |
|
Tuberculosis |
Staining/cultures for Mycobacteria |
Radiological appearance |
Neutrophilic |
Idiopathic pulmonary fibrosis |
HRCT findings |
Moderate increased neutrophil count (10–30%) in 70–90% of patients |
Eosinophils slightly increased (in 40–60% of patients) |
Neutrophils >2× eosinophils |
|
Collagen vascular disease |
Dominantly increased neutrophils |
|
Asbestosis |
Asbestos bodies (negative in 10–15%) |
|
Bacterial infection |
Bacteria on staining and cultures |
Eosinophilic |
Eosinophilic pneumonia |
Eosinophils >25% (up to 90%) |
Eosinophils > neutrophils |
Plasma cells may be present |
Radiological criteria on HRCT |
|
Churg–Strauss syndrome |
Moderate eosinophilia |
|
Allergic bronchopulmonary aspergillosis |
Staining for Aspergillus+ |
Criteria for ABPA |
|
Drug-induced lung disease |
Very variable |
Mixed |
|
Predominant pattern may lead to diagnosis |