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A case of idiopathic juxtafoveolar retinal telangiectasis group 2A Hidenori Takahashi 1 , Ryo Obata 2 , Aya Iriyama 1 , Yuji Inoue 1 , Yasuo Yanagi 1 , Yasuhiro Tamaki 1 1Dept of Ophthalmol,Univ of Tokyo Sch of Med 2Dept of Ophthalmol,Saitama Red Cross Hosp pp.373-378
Published Date 2007/3/15
DOI https://doi.org/10.11477/mf.1410101562
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Abstract. Purpose:To report a case of idiopathic juxtafoveolar retinal telangiectasis group 2A. Case and Findings:A 53-year-old woman,presented with blurring of vision since 2 years before. Her corrected visual acuity was 0.2 right and 0.4 left. Both eyes showed area of grayish opacity temporal to the macula. The right eye showed,additionally,elevation of opaque area with subretinal hemorrhage. The left eye showed crystalline deposits. Fluorescein angiography showed dilated capillaries with dye leakage temporal to the macula,leading to the diagnosis of idiopathic juxtafoveal telangeiectasia group 2A. Optical coherence tomography(OCT)showed disruption in photorecepter layer with lamellar cyst. The elevated opaque lesion in the right eye became atrophic following subtenon injection of triamcinolone. There was no change in visual acuity. The finding was suggestive of subretinal neovascularization. Conclusion:Impaired visual acuity in this clinical entity may be associated with atrophic changes in the retina.


Copyright © 2007, 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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