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Differentiation of uveal effusion from bullous retinal detachment in two cases Makoto Ueno 1 , Yuji Watanabe 1 , Kentaro Uemura 1 , Yoshihisa Miura 1 , Ikuo Watanabe 1 1Dep. of Ophthalmol., Hamamatsu Univ. Sch. of Med. pp.145-152
Published Date 1985/2/15
DOI https://doi.org/10.11477/mf.1410209329
  • Abstract
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We observed two cases of uveal effusion.The first case, a 36-year-old male, presented with bilat-eral peripheral annular choroidal detachment and nonrhegmatogenous shallow retinal detachment. Fluorescein angiography showed pigment epith-elial lesions as Leopard spots in the paramacularand nasal fundus, resulting in diffuse dye leakage from the choroid in the late phase. An increase in protein content was present in the cerebrospinal fluid (59mg/dl). The choroidal and retinal deta-chments subsided spontaneously.

The second case, a 49-year-old female, presented with nonrhegmatogenous bullous detachment of the retina, shifting subretinal fluid and dilated episcleral vessels in the right eye. No choroidal detachment was observed. Fluorescein angiography showed numerous foci of dye leakage from the choroid along the upper vascular arcade. Laser photocoagulation to these foci and drainage of subretinal fluid were futile to improve the retinal detachment. An elevated protein content was seen in the cerebrospinal fluid (160mg/dl). The left eye was free of retinal detachment and showed so-called salt-and-pepper fundus.

This second case was diagnosed as a type of uveal effusion on account of the clinical features including dilated episcleral vessels, elevated protein in the CSF and failure of photocoagulation suggest-ing the venous obstruction as the basic pathogenetic process. An attempt is necessary to differentiate uveal effusion from bullous retinal detachment or multifocal posterior pigment epitheliopathy from the viewpoint of the presumed pathogenesis of uveal effusion.


Copyright © 1985, 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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