Giant Ascending Aortic Aneurysm and Chronic Type A Dissection
Imaging findings
Chest radiograph shows a large right mediastinal convexity. Chest CT demonstrates a giant ascending aortic aneurysm (one of the largest seen) with a chronic type A dissection flap, extensive mural calcification, thrombus, and circumferential intimal intussusception extending into the arch vessels, in a 41-year-old man with a family history of dissection.
Key takeaways
Giant ascending aortic aneurysms are associated with genetic aortopathies/elastopathies (e.g. Marfan syndrome, Loeys-Dietz syndrome, or vascular Ehlers-Danlos). A complete circumferential intimal tear can lead to chronic dissection and intimal intussusception (peeling of the intima into the arch branches), which can be surprisingly asymptomatic or present with minimal chronic symptoms.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Niemann-Pick DiseaseMetabolic
- Diffuse Invasive Mucinous AdenocarcinomaNeoplastic
- Congenital Pulmonary Atresia with Glenn and Potts Shunts and RV-Dependent Coronary CirculationCongenital
- Pulmonary Lymphedema secondary to Sarcoid-like Lymphadenopathy (Humira-Induced)Iatrogenic
- Bacillus cereus PneumoniaInfection
- Veno-Arterial ECMO Flow PatternsIatrogenic
- Cytomegalovirus PneumonitisInfection
- Esophageal Duplication CystCongenital
See all cases from April 9, 2021 →
Related Vascular cases
- Pulmonary Arterial Hypertension associated with Neurofibromatosis Type 1
- Chronic Thromboembolic Pulmonary Hypertension (CTEPH) with Pulmonary Artery Compression of Left Coronary Artery
- Severe CTEPH in a Young Adult with Systemic-to-Pulmonary Collaterals
- Concurrent Venous, Pulmonary Arterial, and Aortic Thrombus (Hypercoagulable State)
- Type A Aortic Intramural Hematoma Misdiagnosed as Aortitis
- Hepatopulmonary Syndrome Type 2 with Pulmonary Vascular Nodules