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Table 1 Etiologies of pediatric uveitis

From: Epidemiology of pediatric uveitis and associated systemic diseases

Etiology

Total N (%)

Categories

N (%)

Median age at uveitis diagnosis, y (IQR)

Systemic treatment, N (%)

Median follow-up, m (IQR)

Idiopathic

101 (65.2)

  

13.0 (10.0–16.0)

39 (38.6)

16.0 (2.0–53.0)

Systemic immune-mediated disease

44 (28.4)

Juvenile idiopathic arthritis

23 (14.8)

11.0 (6.5–16.0)

20 (87.0)

72.0 (2.5–111.0)

 

Behçet disease

10 (6.5)

15.0 (13.3–16.8)

9 (90.0)

120.0 (67.5–132.0)

 

Kawasaki disease

3 (1.9)

11.0 (11.0–12.0)

3 (100)

15.0 (14.5–33.5)

 

Vogt–Koyanagi–Harada syndrome

3 (1.9)

16.0 (15.0–17.0)

2 (66.7)

36.0 (29.0–60.0)

 

Tubulo-intestinal nephritis

2 (1.3)

11.5 (11.3–11.8)

2 (100)

49.5 (38.3–60.8)

 

Systemic lupus erythematosus

1 (0.7)

6

1 (100)

180

 

Kikuchi disease

1 (0.7)

17

1 (100)

35

 

Inflammatory bowel disease

1 (0.7)

13

1(100)

42

Syndrome confined primarily to the eye

5 (3.2)

Trauma

3 (1.9)

12.0 (8.0–16.0)

1 (33.3)

9.0 (7.5–40.5)

 

Posner–Schlossman syndrome

1 (0.7)

18

1 (100)

0.3

 

Sympathetic ophthalmia

1 (0.7)

9

1 (100)

3

Masquerade syndrome

4 (2.6)

Langerhans cell histiocytosis

2 (1.3)

13.0 (11.0–17.0)

1 (50.0)

95.5 (77.3–113.8)

 

Acute lymphocytic leukemia

1 (0.7)

18

1 (100)

60

 

Hydroa vacciniforme-like lymphoma

1 (0.7)

6

1 (100)

16

Infection

1 (0.7)

Varicella zoster virus

1 (0.7)

17

0 (0.0)

21

  1. m months