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A large left ventricular pseudoaneurysm in Behçet's disease: a case report
Seyed Mojtaba Marashi1, Payam Eghtesadi-Araghi, Mohammad Hussein Mandegar
1Department of Cardiac Surgery, Dr. Shariati Hospital Complex, Tehran Univ. of Medical Sciences, Tehran 14197, Iran. marashi@doctor.com
Insights
Behçet
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Vascular Surgery
Background:
- Behçet's disease is a multisystem inflammatory disorder primarily affecting the vascular system.
- While arterial pseudoaneurysms are common, cardiac involvement, particularly left ventricular pseudoaneurysms, is exceptionally rare.
- This condition is more prevalent in Asian and Mediterranean populations.
Observation:
- A case report details a 13-year-old male with a 4-year history of Behçet's disease.
- The patient presented with symptoms including cough, chills, fever, and chest pain.
- Diagnostic imaging, including echocardiography, MRI, CT, and coronary angiography, confirmed a large left ventricular pseudoaneurysm.
Findings:
- Surgical intervention was performed for the left ventricular pseudoaneurysm.
- The patient experienced no complications during a 24-month follow-up period post-surgery.
- This case highlights the potential for rare cardiac manifestations in Behçet's disease.
Implications:
- The nonspecific symptoms of cardiac pseudoaneurysms necessitate a high index of suspicion in Behçet's disease patients.
- Early diagnosis and management are crucial due to the potentially fatal nature of cardiac pseudoaneurysms.
- This case underscores the importance of considering cardiac complications in the long-term management of Behçet's disease.
Background:
Behçet's disease is a collagen-vascular disease most commonly seen in Asia and Mediterranean area. Different organs and systems including cardiovascular system could be involved. Pseudoaneurysm is the most common form of arterial involvement in Behçet's disease; however, cardiac pseudoaneurysm is rare.
Case Presentation:
A rare case of 13 years old boy with a 4-year history of Behçet's disease with development of a huge left ventricular pseudoaneurysm is reported who had been admitted because of cough, chills, fever, and chest pain. Findings obtained on echocardiography, magnetic resonance imaging, chest computed tomography and coronary angiography confirmed a left ventricular pseudoaneurysm. There was no complication for next 24 months follow up period after surgical treatment.
Conclusion:
Considering its fatality and nonspecific manifestations, one should consider cardiac pseudoaneurysms as a potential risk in any patient with Behçet's disease.
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