Abstract 99. Jahrestagung der DOG, 29. 9. - 2. 10. 01 im ICC, Berlin

Anmeldung zur Tagung
   Registration
Grußwort
   Invitation
Themen
   Topics
Allgemeiner Ablauf
   General overview
Wissenschaftliches Programm
   Scientific program
Kurse
   Courses
Symposien
   Symposiums
Frühstück mit Spezialisten
   Breakfast with specialists
Arzthelferinnen-Fortbildung
Rahmenprogramm
   Social program
DOG Information
   DOG Information
Allgemeine Informationen
   General Information
Autorenindex
   Index of Authors
Ausstellerliste
   Exhibitors
Sponsoren
   Sponsors
Teilnahmegebühren
   Registration fees
Impressum



The Differential Diagnosis of not HIV-associated Necrotizing Retinopathies

Schwarz J., Körner U., Garweg J. G.

Univ.-Augenklinik, Inselspital, 3010 Bern

Background: The diagnosis of not HIV-associated necrotizing retinopathies is often difficult to obtain as it usually is lacking laboratory confirmation. A broad differential diagnosis and the importance of immunogenetic influences on the likelihood and frequences of distinct disease groups such as M. Behcet may further contribute.
Patients and Methods: Therefore we reviewed retrospectively the records of all patients with not HIV-associated necrotizing retinopathies who had presented to the uveitis ambulance of our outpatient clinic over the past five years. In all circumstances, a close follow up included clinical course and photo documentation, broad serological investigations, eventually supplemented by aqueous humor analysis, fluorescein angiography and further medical diagnostics according to clinical judgement to generate a differential diagnosis and provide a therapeutic concept.
Results: a definitive diagnosis was obtained in 21/25 cases (84%), usually only after inclusion of the clinical response to therapy. In 9 cases, a infectious etiology was found (atypical toxoplasmosis: 5 cases, a VZVassociated retinal necrosis in 3 and a CMV-associated one in 2 cases). In 8 instances, an underlying immunological disease was confirmed (6 x M. Behcet, 2 x VKH syndrome). Three times, an acute hypertensive retinopathy was misinterpreted as infectious retinal necrosis, and once a severe immunoglobulin deficiency with panophthalmia was diagnosed.
Conclusion: In only 40% of cases an infectious etiology was confirmed, half of which were attributable to atypical ocular toxoplasmosis. The most common immunological disorder was M. Behcet. A clinical affiliation was usually possible in infectious retinopathies, whereas in inflammatory occlusive vasculopathies such as M. Behcet and Lupus-associated retinal vasculitis the clinical course under therapy had to be taken into account for a definitive diagnostic categorization.




DOG HomepageZurück / Back