Behçet’s Disease Occlusive Vasculitis Progressing to Prepapillary Neovascularization

53-year-old man who had recurrent oral and genital aphthous, who consulted urgently for bilateral uveitis that is currently active on the right eye with central and peripheral occlusive vasculitis. The patient was diagnosed with behet’s disease in front of the inflammatory syndrome, ocular involvement and bipolar aphtosis. The management was early based on bolus of methylprednisolone and immunosuppressant, argon laser of ischemic areas. Unfortunately, the evolution was unfavorable with the appearance of prepapillary neovessels and persistence of the macular edema having required several intravitreal injections of anti-VEGF and urgent sessions of PRP with argon laser.