Atypical Anterior Uveitis in Behcet's Disease
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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.
References
I. Ksiaa et al .Ey and Behcet disease.J Fr Ophtalmol.42(6) 626-641 (2019) DOI: https://doi.org/10.1016/j.jfo.2018.09.027
Rokutanda R, Kishimoto M, Okada M. Update on the diagnosis and management of Behçet’s disease. Open Access Rheumatol 2014;30:1–8. DOI: https://doi.org/10.2147/OARRR.S46644
Z Hajji et al Encyclopédie Médico-Chirurgicale.21-225-C-20 (2010)
Yohei Kirini et al Clinical and genetic Aspects of Behcet’s disease in Japan .Intern Med 58(9) 1199-1207 (2019). DOI: https://doi.org/10.2169/internalmedicine.2035-18
Uwe Pleyer et al.Anterior uveitis clinic Diagnostic procedure and treatment options.Klin Monbl Augenheilkd (2020).
Sinem Nihal Esatogln et al.Update on the treatmentof Behcet’s syndrom.Intern Emerg Med 14,661-675 (2019) DOI: https://doi.org/10.1007/s11739-019-02035-1
Jing Zhangetal. A review of behcet’s disease from perspectives of both western and chinese medicine.J Tradit Chi Med39(1) ; 139-152 ( 2019).