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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%)

Mucocutaneous ulceration in Behçet disease

 

 

Oral aphthous ulceration - painful, recurrent

Genital ulceration

 

 

Skin lesions in Behçet disease

Erythema nodosum

Acneiform

Pustule after scratching skin

Lines after stroking skin

(pathergy test)

(dermatographism)

Vascular lesions in Behçet disease

 

 

Migratory thrombophlebitis

Obliterative thrombophlebitis

of extremities

of major internal veins

 

 

Uveitis in Behçet disease

Acute iritis

Retinitis

Occlusive periphlebitis

Diffuse leakage

Signs of Vogt-Koyanagi syndrome

Granulomatous

Alopecia

iridocyclitis

 

Poliosis

Vitiligo

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

UVEAL INFECTIONS AND INFESTATIONS

1.Viruses

Herpes zoster ophthalmicus

Acute retinal necrosis

Cytomegalovirus (CMV)

2.Spirochaetes

Syphilis

Lyme disease

3.Mycobacteria

Tuberculosis

Leprosy

4.Protozoa and worms

Toxoplasmosis

Ocular toxocariasis

5.Fungi

Presumed ocular histoplasmosis syndrome

Candidiasis

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