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. 2016 Feb 1;35(10):2509–2516. doi: 10.1007/s10067-016-3187-z

Table 1.

Summary of the clinical features present in first 6 months from diagnosis, and over the whole disease course in a cohort 46 children with Behçet’s disease in a single UK paediatric rheumatology tertiary centre

Number (%) with feature in the first 6 months (N = 46) Number (%) with feature in whole disease course (N = 46)
Recurrent oral ulceration 38 (82.6) 45 (97.8)
Genital ulceration 8 (17.4) 34 (73.9)
Skin lesions 5 (10.9) 11 (23.9)
 Pustular lesions 1 (2.2) 3 (6.5)
 Skin ulceration 1 (2.2) 2 (4.3)
 Erythema nodosum 1 (2.2) 2 (4.3)
 Necrotizing folliculitis 1 (2.2) 2 (4.3)
 Acneiform lesions 1 (2.2) 2 (4.3)
Pathergy* 0 3/5 (60)
Ocular lesions 1 (2.2) 4 (8.7)
 Anterior uveitis 1 (2.2) 2 (4.3)
 Conjunctivitis 0 2 (4.3)
Gastrointestinal manifestations 12 (26.1) 26 (56.5)
 Abdominal pain 4 (8.7) 12 (26.1)
 Gastrointestinal haemorrhage 1 (2.2) 2 (4.3)
 Gastrointestinal ulceration 2 (4.3) 7 (15.2)
 Anal/perianal ulceration 2 (4.3) 5 (10.9)
 Recurrent diarrhoea 3 (6.5) 6 (13.0)
Fever 13 (28.3) 14 (30.4)
Arthritis 4 (8.7) 10 (21.7)
Neurological manifestations 5 (10.9) 13 (28.3)
 Seizure 0 1 (2.2)
 Frequent headache 5 (10.9) 11 (23.9)
Vascular complication 2 (4.3) 3 (6.5)
 Sagittal sinus thrombosis 1 (2.2) 2 (4.3)
 Thrombophlebitis 0 1 (2.2)
Serositis
 Pericardial effusion 1 (2.2) 1 (2.2)

*Pathergy test was only performed in five patients, and was positive in 3/5