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A case of Vogt-Koyanagi-Harada disease simulating central serous chorioretinopathy in senile persons Naoko Koike 1 , Tsuyoshi Otsuji 1 , Masashi Nakauchi 1 , Motoki Kimura 1 , Tetsuya Nishimura 1 , Kanji Takahashi 1 1Dept of Ophthalmol,Kansai Med Univ pp.1523-1529
Published Date 2011/9/15
DOI https://doi.org/10.11477/mf.1410103846
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Abstract. Purpose:To report a case of Vogt-Koyanagi-Harada(VKH)disease simulating central serous chorioretinopathy in senile persons. Case:A 62-year-old male presented with metamorphopsia and impaired vision in the right eye since 6 months before. Findings:Corrected visual acuity was 0.6 right and 1.2 left. The right eye showed serous retinal detachment in the macular area. Fluorescein angiography showed one point of leakage followed by dye pooling in the subretinal space. Indocyanine green angiography showed delayed dye filling in the choroid. Optical coherence tomography showed serous retinal detachment and moderately reflective reflex suggestive of fibrinous accumulation. Seven months later,serous retinal detachment appeared in the left eye with edema of optic disc in both eyes. Retinal detachment disappeared 2 months later. Both eyes showed sunset-glow fundus another 3 months later. Conclusion:This case illustrates that VKH disease may initially manifest clinical features simulating central serous chorioretinopathy.


Copyright © 2011, 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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