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Recurrent Spontaneous Coronary Artery Dissections in a Male Patient With Fibromuscular Dysplasia
Mersal Samimi1, Naman Jain1, Miro Asadourian2
1Internal Medicine, University of California San Francisco, Fresno, Fresno, USA.
Insights
Spontaneous coronary artery dissection (SCAD) can affect young men, particularly those with fibromuscular dysplasia. This case highlights recurrent SCAD in a young man, emphasizing the need for further research into its causes and treatments.
Area of Science:
- Cardiology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome, typically affecting young to middle-aged women.
- While less common in men, SCAD can occur in younger males, sometimes without traditional cardiovascular risk factors.
- Fibromuscular dysplasia (FMD) is an associated condition that may increase the risk of SCAD recurrence, even in men.
Observation:
- This report details a case of a young man with a history of FMD and previous SCAD in multiple coronary arteries.
- The patient presented with exertional chest pain, indicative of myocardial ischemia.
- Recurrent SCAD was diagnosed in the distal right coronary artery despite ongoing conservative management with aspirin and beta-blockers.
Findings:
- Recurrent SCAD can occur in young men with FMD, even under optimal medical therapy.
- The presentation of exertional chest pain in this case signaled a significant cardiovascular event.
- This case underscores the potential for SCAD recurrence in specific male populations.
Implications:
- Further investigation into the pathophysiology of SCAD and its association with FMD in men is crucial.
- Developing targeted medical therapies for recurrent SCAD in men is a significant unmet need.
- This case highlights the importance of considering SCAD in young men presenting with acute coronary syndromes, especially with a history of FMD.
Abstract:
Spontaneous coronary artery dissection (SCAD) is a rare presentation of acute coronary syndrome characterized by a tearing of the wall of the epicardial coronary artery, leading to myocardial ischemia. SCAD predominantly affects young and middle-aged women, but young men without significant cardiovascular risk factors can also present with the disease. In the setting of fibromuscular dysplasia, men may be at a higher risk for recurrence. We present the case of a young man with a history of fibromuscular dysplasia and prior SCAD in the diagonal branch and right posterolateral artery who presented with exertional chest pain. Further evaluation revealed a recurrent SCAD of the distal right coronary artery despite being on conservative management with aspirin and beta-blockers. There is a need to study the pathophysiology of fibromuscular dysplasia and SCAD in men further and develop medical therapies to treat recurrent SCAD.
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