Table 2.
Systemic and/or ocular diagnosis | n (%) |
---|---|
Behçet’s disease | 1 (1.7) |
Fuchs’ heterochromic uveitis | 12 (20.7) |
Herpes-related uveitis | 3 (5.2) |
HLA-B27-related uveitis | 2 (3.4) |
Idiopathic anterior uveitis | 16 (27.6) |
Idiopathic vasculitis | 1 (1.7) |
Morbus Bechterew | 6 (10.3) |
Polymyalgia/temporalis arteritis | 1 (1.7) |
Possner Schlossman | 1 (1.7) |
Psoriatic arthritis | 2 (3.4) |
Sarcoidosis | 7 (12.1) |
SLE | 1 (1.7) |
Toxoplasmosis | 2 (3.4) |
Ulcerous colitis | 1 (1.7) |
Wegener’s granulomatosis | 2 (3.4) |
| |
Anatomical localizationa | n (%) |
| |
Anterior | 56 (96.6) |
Intermediate | 2 (3.4) |
Posterior | 4 (6.9) |
Pan | 0 |
Notes:
Some eyes had more than one type of uveitis localization; in one eye, uveitis was mainly posterior. The other eyes with posterior and intermediate uveitis also had anterior uveitis.
Abbreviations: SLE, systemic lupus erythematosus; HLA, human leukocyte antigen.