Mucocutaneous Involvement in Behçet’s Disease: How Systemic Treatment Has Changed in the Last Decades and Future Perspectives

Behçet’s disease (BD) is a multisystemic disorder of unknown etiology characterized by the “triple symptom complex” consisting of recurrent oral aphthosis, genital ulcers, and chronic relapsing bilateral uveitis. Recurrent mucocutaneous lesions are generally considered the hallmark of the disease, b...

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Bibliographic Details
Main Authors: Cinzia Rotondo, Giuseppe Lopalco, Florenzo Iannone, Antonio Vitale, Rosaria Talarico, Mauro Galeazzi, Giovanni Lapadula, Luca Cantarini
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2015/451675
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