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Updated: Jun 1, 2026

Novel and Innovative Hybrid Technique for Type A Aortic Dissection
Published on: March 28, 2025
An uncommon presentation of acute type A aortic dissection: left main coronary artery obstruction
Pierre-Yves Courand1, Raphaël Dauphin, Eric Roussel
1Service de Cardiologie, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, 103 Grande Rue de la Croix-Rousse, Lyon Cedex 04, France. pycourand@hotmail.com
Insights
Acute aortic dissection can mimic acute coronary syndrome, sometimes involving the left main coronary artery. This rare presentation can lead to misdiagnosis and delayed treatment for aortic dissection.
Area of Science:
- Cardiology
- Vascular Surgery
Background:
- Acute aortic dissection (AAD) is a life-threatening condition with diverse clinical presentations.
- Misdiagnosis of AAD as acute coronary syndrome (ACS) can lead to inappropriate management and adverse outcomes.
Observation:
- A 64-year-old male presented with ST elevation in aVR and diffuse ST depression, suggestive of ACS.
- Coronary angiography was attempted for primary percutaneous coronary intervention but failed due to inability to catheterize the left main coronary artery.
Findings:
- Aortography and transesophageal echocardiography confirmed Stanford type A aortic dissection.
- The dissection involved the ostium of the left main coronary artery, causing obstruction.
Implications:
- This case highlights the critical importance of considering aortic dissection in patients with atypical ACS presentations.
- Left main coronary artery involvement in Stanford type A aortic dissection is a rare but critical complication.
- Prompt and accurate diagnosis is essential for appropriate management and improved patient outcomes in aortic emergencies.
Abstract:
Acute aortic dissection presents with a wide range of manifestations. Sometimes an acute coronary syndrome is diagnosed instead of aortic dissection leading to inappropriate treatment. We describe a case of acute aortic dissection with the uncommon involvement of the left main coronary artery. A 64-year-old man was referred to our hospital for primary coronary intervention because ECG demonstrated ST elevation in the aVR lead with diffuse ST-segment depression. Coronary angiography was performed to treat the culprit lesion but the left main coronary artery could not be catheterized. Aortography and transesophageal echocardiography confirmed Stanford type A aortic dissection. The patient died of cardiac arrest in spite of cardiopulmonary resuscitation. This case also illustrates how Stanford type A aortic dissection can present with left main coronary artery obstruction.
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