Anti-MDA5 antibody-associated dermatomyositis
Imaging findings
CT scan of a 40-year-old male with a skin rash and rapidly progressive respiratory failure requiring VV-ECMO shows diffuse interstitial opacities, dependent consolidation (DAD pattern), traction bronchiectasis, and subsequent pneumomediastinum.
Key takeaways
Anti-MDA5 dermatomyositis is characterized by amyopathic or hypomyopathic skin lesions and rapidly progressive interstitial lung disease (often manifesting as DAD or acute interstitial pneumonia). It carries a poor prognosis and requires aggressive immunosuppression.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Effusive-constrictive pericarditis secondary to leukemiaNeoplastic
- Effusive-constrictive pericarditis in sickle cell diseaseCongenital
- Unrepaired sinus venosus ASD and PAPVR in a heart transplant recipientCongenital
- Primary esophageal lymphomaNeoplastic
- Beta-thalassemia with extramedullary hematopoiesis and hemosiderosisMetabolic
- Descending necrotizing mediastinitis from cervical necrotizing fasciitisInfection
- Ruptured thoracoabdominal aortic aneurysmVascular
- Incarcerated diaphragmatic liver herniaTrauma
See all cases from October 11, 2019 →
Related Autoimmune cases
- Cellular nonspecific interstitial pneumonia (NSIP)
- Lupus-associated diffuse alveolar hemorrhage
- Anti-synthetase syndrome with acute fulminant lung injury
- Sarcoidosis presenting as cluster-like ground-glass nodules
- IgG4-related lung disease complicated by systemic air embolism
- Heerfordt syndrome (uveoparotid fever) in sarcoidosis