A proposed mild type of acute retinal necrosis syndrome.

Abstract:

:Six patients had peripheral to midperipheral pale yellow retinal exudates typical of acute retinal necrosis syndrome but which extended gradually to the posterior pole and remained isolated without becoming confluent. These exudates resulted in localized retinochoroidal degeneration without retinal detachment, in contrast to acute retinal necrosis syndrome. Antibody titers in aqueous humor were increased to varicella-zoster virus in some of the patients examined. The findings led us to hypothesize that this mild, self-limiting course is one of the natural developments of acute retinal necrosis syndrome, although somewhat modified by corticosteroid or acyclovir therapy, and that acute retinal necrosis syndrome consists of varying degrees of severity from mild to fulminant types.

journal_name

Am J Ophthalmol

authors

Matsuo T,Nakayama T,Koyama T,Koyama M,Matsuo N

doi

10.1016/0002-9394(88)90047-5

subject

Has Abstract

pub_date

1988-06-15 00:00:00

pages

579-83

issue

6

eissn

0002-9394

issn

1879-1891

pii

0002-9394(88)90047-5

journal_volume

105

pub_type

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