Adamantiades-Behçet disease is a primary systemic vasculitis of unknown origin, that may involve blood vessels of all sizes. The clinical hall-mark of Behçet Disease (BD) is oral aphtosis, which is often associated with genital aphtae and a variety of skin lesions. Less common manifestations of BD include thrombophlebitis, central nervous system and ocular inflammation which, however, may impact significant morbidity and mortality.
Behçet's disease: minireview with emphasis on oral aspects
Lo Muzio, Lorenzo
2018-01-01
Abstract
Adamantiades-Behçet disease is a primary systemic vasculitis of unknown origin, that may involve blood vessels of all sizes. The clinical hall-mark of Behçet Disease (BD) is oral aphtosis, which is often associated with genital aphtae and a variety of skin lesions. Less common manifestations of BD include thrombophlebitis, central nervous system and ocular inflammation which, however, may impact significant morbidity and mortality.File in questo prodotto:
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