Introduction Behcet’s disease is a systemic vasculitis characterized by recurrent oral and genital ulcers, cutaneous lesions,ocular,neurological and vascular manifestations.Vascular involvement affects arteries and veins,and includes thrombophlebitis,arterial obstruction and aneurysms.Arteries are less involved than veins,and coronary artery involvement seems to be rare in Behcet’s disease. Objectives: We report a case of 18-year-old man with Behcet’s disease since the age of seven,presenting with acute myocardial infarction due to occlusion of the left marginal artery. Materials & methods: The patient,from Egyptian and Lebanese parents,born on the 21/12/1991,was followed since his childhood for a chronic relapsing inflammatory disease manifesting with recurrent pericarditis,recurrent uveitis,recurrent mouth and anal aphthous and fever,and was considered to have a periodic disease with positive heterozygous mutation.He was on Colchicine 1-2mg since the age of 6 and received sometimes steroids when feeling not so well. He presented with acute chest pain on the 21/10/2008 and was treated on admission with colchicine and NSAIDS for a suspicion of pericarditis,the cardiac enzymes levels were elevated: Troponin:39.9 μg/l (Normal<0.15 μg/l),the diagnosis of myocardial infarction was considered and a treatment with 1 mg/kg per day Prednisone was started with Aspirin,and Heparin. Results: the coronary angiography revealed thrombotic occlusion of the marginal coronary artery with no other anomaly,the cardiac MRI showed a trans mural infarction of the lateral left ventricular wall.The patient had no chest pain on day 2 and the Troponin level decreased to 3.8μg/l on day 7 of treatment,3 months later the patient is very well with no symptoms,on 10 mg/d prednisone, associated with Aspirin and an ACE inhibitor. Discussion & conclusion: The diagnosis of Behcet’s disease was realized upon the history of the patient and the manifestations of his disease which fulfilled criterion for the diagnosis,(recurrent bipolar ulcerations, recurrent uveitis,orchitis,and recurrent pericarditis).Arterial involvement in Behcet’s disease seems to be rare estimated as 7%,manifesting as thrombosis,stenosis,and/or aneurysms.Cardiac involvement is rare,can manifest as granulomatosis endocarditis, myocarditis,arrhythmias,pericarditis.Coronary artery disease with myocardial infarction in Behcet’s disease was found by reviewing the literature in about 26 cases, many with normal coronary arteries on coronary angiography.We present a review of the literature of coronary artery involvement with myocardial infarction in Behcet’s disesase.
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