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Intravitreal ranibizumab was effective for choroidal neovascularization in a case of Vogt-Koyanagi-Harada syndrome Satoko Yui 1 , Wakako Ito 1 , Toshihiko Shiwa 1 , Junko Hori 1 1Dept of Ophthalmol, Nippon Med Sch Hosp pp.1527-1530
Published Date 2015/10/15
DOI https://doi.org/10.11477/mf.1410211519
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Abstract. Purpose:To report a case of Vogt-Koyanagi-Harada disease(VKH)who developed choroidal neovascularization(CNV)that responded to intravitreal ranibizumab. Case:A 56-year-old female was referred to us before. She had been treated by topical and systemic corticosteroid. Findings:Corrected visual acuity was 0.6 right and 0.4 left. Both eyes showed signs of chronic iritis and sunset-glow fundus. Clinical Course:Visual acuity improved to 1.2 in either eye following cataract surgery. Metamorphopsia developed 4 years later with visual acuity of 0.2 right and 0.5 left. Fluorescein angiography and optical coherence tomography showed findings of CNV. Right visual acuity improved to 0.5 following 3 sessions of intravitreal ranibizumab injection over 6 months. She has been doing well for 6 months until present. Conclusion:Repeated sessions of intravitreal ranibizumab was effective for CNV as late complication of VKH.


Copyright © 2015, 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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