Mehdi Khamaily*, Imane Tarib, Yassine Mouzari, Joumany Brahim Salem, Taoufik Abdellaoui, Fouad El Asri, Karim Reda, Abdelbarre Oubaaz
Behcet's disease (BD) is a chronic multisystem disorder, characterized by relapsing inflammation, Ocular involvement
is frequent (40%-70%), and all coats of the eye may be affected. The non-granulomatous character of uveitis is usually
reported in BD.
We report a series of 11 cases of atypically granulomatous uveitis in patients with extra ocular signs of Behcet.