A proposed mild type of acute retinal necrosis syndrome

Toshihiko Matsuo, Tadashi Nakayama, Tetsuro Koyama, Masaya Koyama, Nobuhiko Matsuo

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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.

Original languageEnglish
Pages (from-to)579-583
Number of pages5
JournalAmerican Journal of Ophthalmology
Volume105
Issue number6
Publication statusPublished - Jun 15 1988

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ASJC Scopus subject areas

  • Ophthalmology

Cite this

Matsuo, T., Nakayama, T., Koyama, T., Koyama, M., & Matsuo, N. (1988). A proposed mild type of acute retinal necrosis syndrome. American Journal of Ophthalmology, 105(6), 579-583.