SAoO-Kongress 28.2.2018
Herpetische Uveitis anterior
Prof. Dr. Matthias Becker
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SAoO-Kongress 28.2.2018
In Übergängen denken…
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SAoO-Kongress 28.2.2018
Herpesviridae
• Large family of DNA viruses (>130 herpesviruses) • Large double-stranded, linear DNA genomes• At least five species of Herpesviridae are extremely
widespread among humans• More than 90% of adults have been infected with at
least one of these• Latent form of the virus remains in most people
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Herpesvirus types
Herpesvirus types known to infect humans:1. Herpes simplex virus 1 (HSV-1)2. Herpes simplex virus 2 (HSV-2)3. Varicella-zoster virus (VZV)4. Epstein–Barr virus (EBV)5. Cytomegalovirus (CMV)6. Human herpesvirus 6A (HHV-6A)7. Human herpesvirus 6B (HHV-6B)8. Human herpesvirus 7 (HHV-7)9. Kaposi's sarcoma-associated herpesvirus (KSHV)
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Zoster ophthalmicus• Vesicles on the tip or
the side of the nose• Hutchinson sign• Precedes the
development ofuveitis
• Nasociliary branch ofN. V. innervatesboth: cornea, lateral dorsum of the nose
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Courtesy of D. Goldstein, BCSC
SAoO-Kongress 28.2.2018
Clinical signs (VZV, HSV)
• VZV-uveitis: history of ipsilateral zoster ophthalmicus• Varicella-zoster sine herpete: anterior uveitis without prior
cutaneous component• Variable corneal involvemet (keratouveitis) • Decreased corneal sensation (diffuse or localized)• Anterior, posterior synechiae• Hypopyon (hemorrhagic)
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Übersicht Endothel-Präzipitate
Granulomatös („speckig“)• Sarkoidose, Tuberkulose, MS (beidseitig)• Herpetische Uveitis (einseitig)
Nicht-granulomatös• Fein
• Ankylosierende Spondylitis, HLA-B27+ AAU• Sternförmig-diffus
• Fuchs Uveitis Syndrom
SAoO-Kongress 28.2.2018
DD: Präzipitate - granulomatös
SAoO-Kongress 28.2.2018
DD: Nicht-granulomatös / fein
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DD: Nicht-granulomatös/ sternförmig
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Keratic precipitates
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• Large, central greasy• Fine stellate, diffusely
distributed
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Iris atrophy
• Patchy or sectoral• Pupil dilated
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Atrophy of irispigment epitheliumnot just anteriorstroma
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Ocular hypertension
• Trabeculitis• Frequent complication (DD: toxoplasmosis)• Other uveitides: decreased IOP (ciliary body
hyposecretion)
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Clinical signs (CMV)
• Immunocompetent adults• Chronic or recurrent, unilateral, anterior uveitis, mild
AC activity• Ocular hypertension• Corneal edema• Variable degrees of sectoral iris atrophy• No corneal scars, no posterior synechiae, no flare or
fibrin and no posterior segment involvement
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CMV
• Fails to respond to corticosteroids and high doses ofacyclovir
• Can present as acute relapsing hypertensive anterioruveitis, also known as Posner-Schlossman syndrome(PSS); half of all presumed cases of PSS are CMV-positive
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Epstein-Barr Virus
• Associated with infectious mononucleosis (IM), Burkittlymphoma, nasopharyngeal carcinoma, Hodgkin disease, and Sjögren syndrome
• Primary infection in the context of IM: mild, self-limitingfollicular conjunctivitis
• Most ocular disease is self-limiting and does not require treatment
• Topical corticosteroids and cycloplegia
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Diagnostic options
• Aqueous tap• Real-time PCR analysis• Goldmann-Witmer coeffizient
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Therapeutic management: Topical
• Corticosteroids• Cycloplegics• Antiviral drugs (Zovirax) for keratouveitis (to prevent
dendritic keratitis as a complication of topicalcorticosteroid therapy)
• Prolonged topical antiviral therapy is associated with thedevelopment of keratopathy
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Therapeutic management: Systemic
HSV or VZV (higher doses) :• Acyclovir (Zovirax, 400– 800 mg, 5 times/day)• Valacyclovir (Valtrex, 500 mg to 1 g, 2 times/day)• Famciclovir (Famvir, 250–500 mg, 3 times/day)
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Prophylactic therapy
HSV: • Acyclovir, 400 mg 2 times/day• Valacyclovir, 500 mg/day
VZV • Acyclovir, 800 mg 2 times/day• Valacyclovir, 1 g/day
Immunization• VZV (Zostavax)
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Take home message
• Diagnosis often made clinically• Viable therapeutic options available• Role of corticosteroids• Sometimes long-term therapy necessary
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