Ординатура / Офтальмология / Английские материалы / Illustrated Tutorials in Ophthalmology Kanski, Bolton 2001
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Behçet5 Disease
1.Idiopathic multisystem disease
2.Presentation - third to fourth decade
3.Most prevalent in Mediterranean region and Japan
4.Associated with HLA-B5 in Turkey and Japan
5.Major diagnostic criteria
•Oral aphthous ulceration (100%)
•Genital ulceration (90%)
•Skin lesions (80%)
•Uveitis (70%)
Skin lesions in Behçet disease
Erythema nodosum |
Acneiform |
Pustule after scratching skin |
Lines after stroking skin |
(pathergy test) |
(dermatographism) |
Uveitis in Behçet disease
Acute iritis |
Retinitis |
Occlusive periphlebitis |
Diffuse leakage |
Harada syndrome
Progression of Harada disease
|
|
|
Multifocal choroiditis |
Multifocal sensory retinal |
Exudative retinal |
|
detachments |
detachment |
|
|
|
Inflammatory bowel disease
Ulcerative colitis |
Crohn disease |
• Large bowel ulceration |
• Stricture and ‘rose thorn’ |
|
ulceration |
||
Acute iritis - uncommon |
||
• Acute iritis - uncommon |
||
|
Tubulointerstitial nephritis and uveitis (TINU)
Renal histology |
Urine |
• |
Most frequently affects women and children |
• Proteinuria and renal |
• |
Hypersensitivity reaction to drugs |
failure |
• |
Bilateral, recurrent anterior uveitis |
• Good response to systemic |
|
|
steroids |
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