Desquamative Interstitial Pneumonia
Differential Diagnosis
- Respiratory bronchiolitis associated interstitial lung disease
- Langerhans cell histiocytosis
- Giant cell interstitial pneumonia
- Usual interstitial pneumonia
- Acute eosinophilic pneumonia
- Postobstructive pneumonia
- Infection and other specific processes
Respiratory Bronchiolitis Associated Interstitial Lung Disease | Desquamative Interstitial Pneumonia |
---|---|
Patchy | Diffuse pulmonary involvement |
Intra-alveolar macrophages only focally present | Diffuse intra-alveolar macrophages |
Mild pneumocyte hyperplasia | Prominent pneumocyte hyperplasia |
Peribronchiolar thickening | Interstitial thickening |
Langerhans Cell Histiocytosis | Desquamative Interstitial Pneumonia |
---|---|
Intra-alveolar macrophages only focally present | Diffuse intra-alveolar macrophages |
Temporal heterogeneity | Temporally uniform |
Focal or multifocal disease | Diffuse disease |
Numerous eosinophils | Occasional eosinophils |
Cystic change frequent | No cystic change |
Produces stellate scars | Lacks scarring |
Histiocytes with folded nuclei | Histiocytes with round nuclei |
Langerhans cells positive for CD1a and langerin | Macrophages CD1a and langerin negative |
Giant Cell Interstitial Pneumonia | Desquamative Interstitial Pneumonia |
---|---|
Centrilobular distribution | Diffuse intra-alveolar macrophages |
Numerous multinodular giant cells | Giant cells not present |
Heavy metal may be identified | No heavy metals |
Usual Interstitial Pneumonia | Desquamative Interstitial Pneumonia |
---|---|
Intra-alveolar macrophages only focally present | Diffuse intra-alveolar macrophages |
Temporal heterogeneity | Temporally uniform |
Architecture destroyed, honeycomb change prominent | Architecture preserved, honeycomb change uncommon |
Fibroblastic foci common | Fibroblastic foci absent |
Interstitial fibrosis marked | Interstitial fibrosis mild to moderate |
Interstitial fibrosis variably distributed | Interstitial fibrosis tends to be more uniform |
Desquamative Interstitial Pneumonia | Acute Eosinophilic Pneumonia |
---|---|
Subacute onset | Acute, fulminant onset |
Eosinophils infrequent | Prominent eosinophils in lavage and biopsy specimens |
Post-obstructive Pneumonia | Desquamative Interstitial Pneumonia |
---|---|
Foamy macrophages | Finely granular macrophages |
No pigment in macrophages (unless a smoker) | Pigment in macrophages |
No interstitial pneumonitis | Interstitial pneumonitis present (but mild) |
Localized | Generalized |
- Infection must always be ruled out
- Especially important in immunosuppressed patients
- Atypical mycobacteria may simulate this pattern
- Asbestosis and drug reactions should be ruled out clinically and by searching for asbestos bodies
- Amiodarone may produce non-pigmented coarsley foamy macrophages
- Usually associated with organizing pneumonia or acute interstitial pneumonia