Acute Interstitial Pneumonia - Diffuse Alveolar Damage
Differential Diagnosis
- Usual interstitial pneumonia
- Nonspecific interstitial pneumonia
- Cryptogenic organizing pneumonia
- Cryptogenic organizing pneumonia
- Infection and other specific processes
Usual Interstitial Pneumonia | Acute Interstitial Pneumonia |
---|---|
Temporal heterogeneity | Temporally uniform |
Honeycomb change prominent | Honeycomb change only in late stage |
Patchy distribution with subpleural accentuation | Diffuse, uniform throughout |
Hyaline membranes not seen | Hyaline membranes prominent in early stage |
Nonspecific Interstitial Pneumonia | Acute Interstitial Pneumonia |
---|---|
Predominantly interstitial | Prominent intra-alveolar component |
No hyaline membranes | Hyaline membranes prominent in early stage |
Intra-alveolar organization rare and focal | Prominent intra-alveolar organization in intermediate stage |
Honeycomb change rare | Diffuse honeycomb change may be seen in late stage |
Insidious onset, chronic disease | Acute onset |
Cryptogenic Organizing Pneumonia | Acute Interstitial Pneumonia |
---|---|
Patchy distribution | Diffuse |
No hyaline membranes | Hyaline membranes prominent in early stage and fragments in organizing phase |
No collagen deposition, architecture preserved | Diffuse honeycomb change may be seen in late stage |
Acute Interstitial Pneumonia / Diffuse Alveolar Damage | Acute Eosinophilic Pneumonia |
---|---|
Eosinophils infrequent | Prominent eosinophils in lavage and biopsy specimens |
Not steroid responsive, poor prognosis | Steroid responsive, no relapses |
- Specific causes of DAD pattern must always be ruled out
- These include infection, aspiration, shock, toxins, burns, transfusions and drugs
- DAD pattern may be superimposed on a chronic process such as UIP
in the setting of an acute exacerbation
- Defining feature
- Hyaline membranes, intact or organizing
- Features that should suggest superimposed AIP/DAD
- Squamous metaplasia of respiratory bronchioles
- Fibrin thrombi in small arteries
- Type II pneumocyte hyperplasia
- Clinical and radiographic history is important
- Defining feature