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Pulmonary and cardiac involvement in Behçet disease: 3 case reports
Zeynep Ilerisoy Yakut1, Kemal Odev
1Department of Radiology, Fatih University Medical School, Ankara, Turkey. drilerisoy@gmail.com
Insights
Behçet disease rarely affects the lungs and heart, leading to serious complications. Advanced imaging like CT and MRI angiography can detect vascular issues, offering a safer alternative to traditional angiography.
Area of Science:
- Cardiovascular Imaging
- Rheumatology
- Pulmonology
Background:
- Behçet disease is a rare multisystem inflammatory disorder.
- Pulmonary and cardiac involvement, though infrequent, can be life-threatening.
- Vascular complications are a significant concern in Behçet disease.
Purpose of the Study:
- To present imaging findings in three patients with Behçet disease.
- To highlight the utility of computed tomography and magnetic resonance angiography.
- To discuss the association of pulmonary vascular disease with cardiac complications.
Main Methods:
- Retrospective review of three patients with Behçet disease.
- Computed tomography angiography (CTA) and magnetic resonance angiography (MRA) were utilized.
- Surgical and conventional angiography findings were used for confirmation.
Main Results:
- One patient presented with bilateral pulmonary artery aneurysms, one ruptured and thrombosed.
- Another patient had unilateral pulmonary artery aneurysm with thrombosis and intracardiac thrombus.
- The third patient exhibited unilateral pulmonary artery aneurysm, thrombus, and coronary artery aneurysm.
Conclusions:
- Noninvasive imaging modalities like CTA and MRA are valuable for assessing pulmonary and cardiac involvement in Behçet disease.
- These methods offer a safer alternative to conventional angiography, minimizing endothelial damage.
- Early detection and management of vascular complications are crucial for improving patient outcomes.
Abstract:
Pulmonary and cardiac involvement in Behçet disease is rare but can cause life-threatening complications. This report presents computed tomography and magnetic resonance angiography findings in 3 patients with Behçet disease. Imaging findings were confirmed by surgery in 1 patient and by angiography in another. One patient had bilateral pulmonary artery aneurysms, 1 of which had already ruptured and had thrombosed. The other had unilateral pulmonary artery aneurysm and thrombosis accompanied with intracardiac thrombus formation. The third patient had unilateral pulmonary artery aneurysm, thrombus, and coronary artery aneurysm. As in our case, there have been rare reports of coronary artery disease and intracardiac thrombus formation associated with pulmonary vascular involvement. Noninvasive imaging modalities minimize any risk of endothelial damage and can be an alternative to angiography in assessment of pulmonary and cardiac involvement in Behçet disease.
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