Aortic interruption
▶ Watch on YouTube — age-restricted, cannot embed here
Imaging findings
Widened mediastinum, rib notching, and extensive collateral vessels supplying the descending aorta. The descending aorta does not attach to the aortic arch, consistent with type A aortic interruption.
Key takeaways
Aortic interruption is a rare congenital anomaly characterized by the absence of continuity between the aortic arch and the descending aorta, requiring development of extensive collateral circulation. It is classified by the location of the break.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Metastatic myocardial calcificationMetabolic
- Mycobacterium avium complex (MAC)Infection
- Flavoring worker's lung (constrictive bronchiolitis)Exposure
- Anomalous coronary artery originCongenital
- Elastofibroma dorsiNeoplastic
- Primary pericardial mesotheliomaNeoplastic
- Left lower lobe sequestrationCongenital
- Right middle lobe bronchial atresiaCongenital
See all cases from April 18, 2014 →
Related Congenital cases
- Anomalous Left Circumflex Artery from the Pulmonary Artery
- Tricuspid Atresia with Coronary Sinusoids
- Williams Syndrome with Supravalvular Aortic Stenosis and Pulmonary Artery Narrowing
- Alveolar Capillary Dysplasia with Unroofed Coronary Sinus (Right-to-Left Shunt)
- Primum Atrial Septal Defect (ASD)
- Unroofed Coronary Sinus (Isolated Finding)