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Japanese

Intraocular neovascularization associated with uveitis Sumie Kawahara 1 , Yuko Miyamoto 1 , Yoshihiro Morimura 1 , Annabelle A. Okada 1 , Tetsuo Hida 1 1Dept of Ophthalmol, Kyorin Univ Sch of Med pp.1735-1741
Published Date 2001/10/15
DOI https://doi.org/10.11477/mf.1410907532
  • Abstract
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We observed three cases of intraocular neovascularization associated with uveitis. They were Vogt-Koyanagi-Harada (VKH) syndrome, Behçet disease and tuberculous retinal vasculitis respectively. In the case of VKH syndrome, both eyes showed serous retinal and choroidal detachment in the posterior fundus, and disc neovascularization (NVD). Pulse corticosteroid therapy induced regression of NVD. In the case of Behçet disease, topical corticosteroid and oral cyclosporin induced regression of NVD and retinal neovascularization. In the case of tuberculous retinal vasculitis, systemic antituberculosis therapy and corticosteroid induced resolution of intraocular inflammation and retinal neovascularization. After acute ocular inflammation had subsided, laser photocoagulation was applied to the peripheral nonperfused retina in the case of VKH syndrome and tuberculous retinal vasculitis. There was no recurrence of intraocular inflammation following laser treatment. These cases illustrate that treatment for causative uveitis may result in regression of intraocular neovascularization.


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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