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A young boy with affected heart and mind: arterial involvement in a patient with undiagnosed Behçet's disease
Ulvi Yalcin1, Kadri Murat Gurses, Duygu Kocyigit
1Department of Cardiology, Hacettepe University, Ankara, Turkey. ulviyalcin@gmail.com.
Insights
Behçet
Area of Science:
- Vascular Medicine
- Rheumatology
- Neurology
Background:
- Behçet's disease is a rare multisystem vasculitis.
- It commonly presents with oral/genital ulcers, skin lesions, uveitis, and potential organ involvement.
- Diagnosis can be challenging due to varied manifestations.
Abstract:
Behçet's disesase is a vasculitis that manifests with oral and genital ulcerations, skin lesions, uveitis, vascular, central nervous system and gastrointestinal involvement. While most patients develop mucocutaneous and genital ulcers along with eye disease, other patients may also present with arthritis, frank vasculitis, thrombophlebitis and central nervous system disease. This is the first case in the literature, where the diagnosis of Behçet's disease was made secondary to concomitant involvement of coronary and carotid arteries.
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