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Published on: April 15, 2021
Coronary artery aneurysms in Behçet's disease
Cihan Cevik1, Mohammad Otahbachi, Kenneth Nugent
1Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA. drcihancevik76@yahoo.com
Insights
Behçet's disease, a rare autoimmune condition, can uncommonly affect coronary arteries. This case highlights significant coronary artery aneurysms in a patient with Behçet's disease, emphasizing the need for cardiac screening.
Area of Science:
- Cardiology
- Rheumatology
- Autoimmune Diseases
Background:
- Behçet's disease is a rare chronic autoimmune vasculitis.
- Vascular involvement typically affects veins more than arteries.
- Coronary arterial involvement is exceptionally rare in Behçet's disease.
Observation:
- A 41-year-old man with a history of Behçet's disease presented with significant coronary artery aneurysms.
- The patient had been in remission from Behçet's disease for 13 years.
- The aneurysms were detected during cardiac assessment.
Findings:
- The case report details significant coronary artery aneurysms in a patient with Behçet's disease.
- This finding is unusual given the typical vascular manifestations of the disease.
- The patient's long-term remission did not preclude the development of coronary artery aneurysms.
Implications:
- This case underscores the importance of considering cardiac complications in patients with Behçet's disease, even during remission.
- Routine non-invasive cardiac assessment is crucial for early detection of vascular abnormalities.
- Further research may be needed to understand the specific risk factors and management strategies for coronary aneurysms in Behçet's disease.
Abstract:
Behçet's disease is a rare chronic autoimmune vasculitis with characteristic skin findings. Vascular involvement generally affects veins more than arteries, and coronary arterial involvement is extremely uncommon. Here we report the significant coronary artery aneurysms detected in a 41-year-old man with Behçet's disease who had been in remission for 13 years. Our case illustrates the necessity of initial non-invasive cardiac assessment of patients with Behçet's disease.
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