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A case of congenital arteriovenous communications of the retina Yasuhiro Tsuda 1 , Keisuke Seki 1 , Yoshiharu Kobayashi 1 1Dept of Ophthalmol, Teikyo Univ Sch of Med pp.925-929
Published Date 2001/5/15
DOI https://doi.org/10.11477/mf.1410907338
  • Abstract
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A 26-year-old woman presented with exotropia as the chief complaint. Her corrected visual acuity was nolight perception right and 1.2 left. Funduscopy showed arteriovenous communications of the retina involving all the vesselsin her right eye. The finding was compatible with the diagnosis of Wybern-Mason syndrome. Fluorescein angiographyshowed dye filling in all the affected retinal vessels. Indocyanine green angiography showed a direct communicationbetween retinal and choroidal veins. The choroidal vessels showed no remarkable malformations. Optical coherencetomography (OCT) showed multilobular lacunae located at various levels in the retina consistent with convoluted vesselsprotruding from the retina. To our best knowledge, this is the first report on this syndrome regarding the venovenousanastomosis between the retina and the choroid as well as OCT findings.


Copyright © 2001, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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