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Behcet's syndrome is a chronic, multisystemic inflammatory disorder of unknown origin. The syndrome is characterised by recurrent oral and genital ulcers, eye and skin lesions, arthritis, central nervous system disorders and vascular disease. Recurrent oral ulceration is considered one of the most important manifestations of the syndrome and is central to the diagnosis according to the classification criteria. A clinical case is presented in which the patient seeks care for her recurrent aphthous lesions and through multidisciplinary care the diagnosis is reached.