DOI: https://doi.org/10.36347/sjmcr.2026.v14i05.019

Pages: 945-947

Behçet’s disease is a chronic, relapsing, multisystem inflammatory vasculitis characterized by a wide spectrum of clinical manifestations, predominantly involving mucocutaneous features. We report the case of a 31-year-old patient presenting with recurrent oral and genital aphthosis associated with acneiform skin lesions. The diagnosis of Behçet’s disease was established based on international clinical criteria. Treatment with colchicine resulted in a favorable outcome. This case highlights the importance of early diagnosis in order to prevent systemic complications.