“…2 Behçet's disease is rare, chronic, relapsing, inflammatory, and multisystemic 3,4 and can provoke mucocutaneous, ocular, vascular, cardiac, neural, and gastrointestinal manifestations. 5 The international diagnostic criteria for BD are recurrent oral ulceration (apthous ulcerations that recur three or more times in a 12-month period) and at least two of the following: recurrent genital ulceration (apthous ulcer or scabs), ocular lesions (anterior uveitis or retinal vasculitis), cutaneous lesions (erythema nodosum, pseudofolliculitis, or papulopustular lesions), and pathergy (skin hyperreactivity test in response to a minimal trauma, with readings in 24-48 hours) 6,7 Vascular involvement is one of the primary predictors of morbidity and mortality in BD, with a negative impact on prognosis. 8 Behçet's disease is considered a systemic vasculitis when vascular involvement is present.…”