Acute progressive multifocal Best's disease in a 61-year-old man

American Journal of Ophthalmology
T A Ciulla, A R Frederick

Abstract

To report acute progressive multifocal Best's disease in patients in their seventh decade. We report one such case. We examined a 61-year-old man with strikingly symmetric, 1-disk diameter serous retinal detachments involving each fovea. Fluorescein angiography was unremarkable, with no dye leakage. Electrophysiologic testing confirmed the diagnosis. Visual acuity decreased, and within 1 month, the size and number of lesions rapidly increased. Three months later, the lesions quickly evolved to the classic vitelliform stage. This well-documented case expands the spectrum of findings in multifocal Best's disease.

References

Nov 1, 1977·The British Journal of Ophthalmology·R C FletcherW Rimm
Jun 1, 1977·Archives of Ophthalmology·S A Miller
Jul 1, 1982·Archives of Ophthalmology·T A WeingeistR C Watzke
Jul 1, 1982·Archives of Ophthalmology·G T FrangiehS L Fine

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Citations

Apr 1, 2016·Ophthalmic Genetics·Jingshu LiuGezhi Xu
Feb 6, 2017·Progress in Retinal and Eye Research·Adiv A JohnsonAlan D Marmorstein
Jun 11, 2002·Retina·Richard G BryanDanielle L Costa
Sep 30, 2021·International Ophthalmology Clinics·Abraham Scaria

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