MALADIE DE BEHCET. MALADIES AUTO-‐INFLAMMATOIRES. G. KAPLANSKI. Service de Médecine Interne, CH Concep`on,. Marseille. INSERM UMR_S La maladie de Behçet autochtone. À propos de 73 cas. Rev Rhum 4. Yurdakul S., et al. The prevalence of Behçet’s syndrome in a rural area. Behçet’s disease: from Hippocrates to the Third Millenium. Br J Ophthalmol ; 3 Wechsler B, Du-Boutin LTH, Amoura Z. Maladie de Behçet.
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These complications worsen the prognosis of BD. Vascular manifestations affect particularly young men, during the first years following onset of the disease.
Superficial and deep lower limb thrombosis is the most frequent venous complications but one third of venous thrombosis concern large vessels such as cerebral venous thrombosis, pulmonary embolism, and inferior or superior vena cava, etc. Budd-Chiari syndrome is the worst prognostic factor increasing mortality by 9 times.
Main locations of arterial lesions are aortic abdominal and thoracicfemoral, pulmonary and iliac arteries. Aneurysms are the most severe arterial complications, particularly pulmonary aneurysms associated with a high risk of massive bleeding. Coronary lesions complicated to myocardial infarction are the most severe cardiac complications.
Treatment is based on corticosteroids and immunosuppressive drugs. The use of anticoagulation in venous thrombosis is still controversial.
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Maladie de Behçet de l’enfant – EM|consulte
Boutin aJ. Piette aP. Outline Masquer le plan. Pronostic des atteintes vasculaires. Top of the page – Article Outline.
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