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Alveolar Sarcoid
General Considerations
- Least common manifestation of sarcoid in the lungs (2%)
- Several large airspace “masses” frequently with air bronchograms
- Occurs when granulomas become confluent and compress airspaces
Clinical Findings
- May have an abrupt onset and may change rapidly
Imaging Findings
- Bilateral, multifocal, ill-defined nodules mimicking airspace disease
- May be peripheral in lung, like pulmonary infiltrates with eosinophilia
- “Masses” with air bronchograms
- May very rarely have cavitation
- Gallium 67 will be taken up in sarcoid and may show extranodal sites of involvement, but is not specific
Differential Diagnosis
- Alveolar cell carcinoma
- Lymphoma
- Alveolar proteinosis
- Multifocal pneumonia
Treatment
- Alveolar sarcoid tends to improve with or without steroids
Complications
- High risk for spontaneous pneumothorax
Prognosis
- The “airspace” component of pulmonary sarcoid invariably disappears
- Reticulonodular disease may remain
Alveolar Sarcoid. Frontal chest radiograph at left demonstrates multiple, scattered mass-like densities with irregular margins. The disease affects primarily the periphery of the lungs. A CT scan of another patient with alveolar sarcoid (right) shows multiple patchy densities with air bronchograms (black arrows).
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