Sarcoidosis Superimposed on Alpha-1 Antitrypsin Deficiency
Imaging findings
High-resolution chest CT shows classic panlobular emphysema with severe lower-lobe-predominant lung destruction and vascular reduction due to alpha-1 antitrypsin deficiency. Superimposed on this, there are diffuse, tiny, symmetric micro-nodules with a perilymphatic and subpleural distribution along the fissures, with biopsy-proven non-necrotizing granulomas in the skin.
Key takeaways
Sarcoidosis and alpha-1 antitrypsin deficiency can coexist. The typical perilymphatic and subpleural nodular pattern of pulmonary sarcoidosis remains identifiable even in regions of severe panlobular emphysema, though the nodules may appear more subtle or mimic ground-glass opacities.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Duchenne Muscular Dystrophy CardiomyopathyCongenital
- Cardiac Amyloidosis with Left Atrial DominanceMetabolic
- Eosinophilic Granulomatosis with PolyangiitisAutoimmune
- Tendyne Transcatheter Mitral Valve ReplacementArtifact
- Iatrogenic Brachiocephalic Artery to Innominate Vein FistulaIatrogenic
- Unicuspid Aortic ValveCongenital
- Fontan Palliation Progression for Tricuspid AtresiaCongenital
- Pulmonary Arteriovenous Malformation with Systemic Collateral SupplyCongenital
See all cases from February 18, 2017 →
Related Autoimmune cases
- Granulomatosis with Polyangiitis (GPA) presenting as Diffuse Alveolar Hemorrhage
- Granulomatosis with Polyangiitis (GPA) with Tracheobronchial and Nodular Involvement
- Diaphragmatic Crural Hypertrophy in Stiff-Person Syndrome
- Pulmonary Vein Stenosis Secondary to Sarcoidosis
- Sarcoidosis-Induced Pulmonary Vein Stenosis Treated with Endovascular Stenting
- Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss)