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. 2018 Dec 3;24:8734–8749. doi: 10.12659/MSM.910749

Table 3.

Distribution of final diagnoses by anatomical classification in the single center retrospective observational study from Poland (2005–2015) (number of patients, %).

Idiopathic Toxoplasmosis Fuchs uveitis White dot syndromes Toxocariasis Sarcoidosis HLA B-27 AAU Multiple sclerosis Ankylosing spondylitis Viruses RIS Rheumatoid arthritis IRVAN Tuberculosis Reiter syndrome Juvenile idiopathic arthritis Ulcerative Colitis Hepatitis C Boreliosis
Anterior 9 (12) 0 34 (45.9) 0 0 2 (2.7) 16 (21.6) 1 (1.35) 8 (10.8) 0 0 1 (1.35) 0 0 1 (1.35) 1 (1.35) 1 (1.35) 0 0
Intermediate 24 (66.6) 0 0 0 0 4 (11) 0 4 (11) 0 0 3 (8.3) 0 0 0 0 0 0 1 0
Posterior 23 (16.6) 48 (35.5) 0 29 (21) 16 (11.8) 4 (2.96) 0 0 0 6 (4.3) 1 (0.7) 1 (0.74) 4 (2.9) 2 (0.7) 0 0 0 0 1
Panuveitis 10 (29.4) 2 (5.6) 0 0 1 (2.8) 7 (20.6) 0 8 (23.5) 2 (5.6) 1 (2.1) 1 (2.9) 2 (5.6) 0 0 0 0 0 0 0
Total No. (%) 66 (23.7) 50 (17.9) 34 (12.2) 29 (10.4) 17 (6.1) 17 (6.1) 16 (5.7) 13 (4.7) 10 (3,6) 7 (2.5) 5 (1.8) 4 (1.4) 4 (1.4) 2 (1.5) 1 (0.36) 1 (0.36) 1 (0.36) 1 (0.36) 1 (0.36)

HLA-B27 AAU – HLA-B27 associated acute anterior uveitis (AAU) without systemic disease; RIS – radiologically isolated syndrome, or demyelinating changes on magnetic resonance imaging (MRI) without clinical signs of multiple sclerosis [17]; WDS – white dot syndrome, a group of inflammatory disorders that affect the outer retinal layers, retinal pigment epithelium (RPE) and/or choroid [18]; IRVAN – idiopathic retinal vasculitis, aneurysms, and neuroretinitis.