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Right ventricular outflow tract thrombus in a case of Behcet's disease
Necla Ozer1, Orçun Ciftçi, Metin Demirci
1Cardiology Department, Hacettepe University, Faculty of Medicine, Ankara, Turkey. neclaozer@hotmail-com
Insights
Behcet's disease, a vasculitic syndrome, rarely involves the heart. This case study details a young woman who developed a right ventricular thrombus during medical treatment for Behcet's disease.
Area of Science:
- Cardiology
- Rheumatology
- Systemic Vasculitis
Background:
- Behcet's disease is a chronic systemic vasculitic syndrome characterized by oral/genital ulcers and uveitis.
- Vascular complications, primarily thrombosis, affect up to one-third of patients.
- Cardiac involvement in Behcet's disease is exceptionally rare.
Observation:
- A young female patient with Behcet's disease was undergoing medical treatment.
- The patient developed a thrombus in her right ventricle.
Findings:
- The case highlights an unusual cardiac manifestation of Behcet's disease.
- Right ventricular thrombus formation occurred during medical management.
Implications:
- This case underscores the importance of considering cardiac complications in Behcet's disease, even when rare.
- Further investigation into cardiac involvement in Behcet's disease may be warranted.
- Understanding rare cardiac manifestations can refine patient monitoring and treatment strategies.
Abstract:
Behcet's disease is known as a chronic systemic vasculitic syndrome, the hallmark of which is recurrent oral aphthous and genital ulcerations and uveitis. Vascular involvement, mainly thrombosis, reportedly affects as many as one-third of patients. Cardiac involvement, however, is very rare. We present in this report a young female patient developing right ventricular thrombus while being treated medically.
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