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[Intracardiac thrombosis: unusual complication of Behcet's disease]
Mannoubia Fekih1, Sana Fennira, Lilia Ghodbane
1Service de Cardiologie "Adultes", Hôpital La Rabta, Tunis.
Insights
Behcet
Area of Science:
- Cardiology
- Rheumatology
- Vascular Medicine
Background:
- Behcet's disease is a rare multisystem inflammatory disorder.
- Cardiac involvement, particularly intracardiac thrombosis, is exceptionally uncommon in Behcet's disease.
Observation:
- A 29-year-old male presented with symptoms of right heart failure, thrombophlebitis, and pulmonary embolism.
- Echocardiography, computed tomography, and magnetic resonance imaging revealed a right atrial thrombosis.
Findings:
- The patient was diagnosed with Behcet's disease based on recurrent aphthous ulcers and hypersensitivity.
- This case highlights an unusual presentation of Behcet's disease with intracardiac thrombosis.
Implications:
- Behcet's disease should be considered in young males from the Mediterranean basin presenting with cardiac thrombosis.
- Early recognition and management are crucial for patients with Behcet's disease and cardiovascular manifestations.
Abstract:
Cardiac involvment is rare, and intracardiac thromboses are exceptional in Behcet's disease. We present a 29 years old male patient seen for right heart-failure, thrombophlebitis and pulmonary embolism. A right atrial thrombosis was showen at the echocardiography and confirmed by computed tomography and magnetic resonance imaging. The diagnosis of Behcet's disease was established on the finding of bipolar aphtous ulcers and skin hypersensitivity. We conclude that Behcet's disease shoud be considered as a possible cause of cardiac thrombosis in the youngs men of the Mediterranean basin.
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