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A case of punctate inner choroidopathy with subretinal fibrosis Ken Itoh 1 , Toshiaki Kubota 1 , Miwako Yamashiro 1 , Yukinori Harada 1 , Akihiko Tawara 1 , Satoshi Sugahara 2 , Yukiko Nakanishi 3 , Naofumi Hirose 4 1Dept of Ophthalmol,Univ of Occupational and Environmental Health,Japan 2Sugahara Eye Clin 3Dept of Ophthalmol,Skin Kokura Hosp 4Sakka Eye Clin pp.1157-1162
Published Date 2006/7/15
DOI https://doi.org/10.11477/mf.1410100885
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Abstract. Purpose:To report a case of punctate inner choroidopathy with choroidal neovascularization resulting in subretinal fibrosis. Case and Findings:A 25-year-old female noted scotoma and metamorphopsia in her left eye. The left eye,reportedly,showed yellow spots distributed over the fundus and neovascularization temporal to the fovea. Corrected visual acuity was 0.1 when seen by us 7 months later. Site of neovascularization had turned into subretinal fibrous tissue. Systemic corticosteroid was followed by gradually improved visual acuity. Yellow spots and subretinal fibrosis turned into pigmented scarred tissue. Conclusion:She was diagnosed with punctate inner choroidopathy based on choroidal neovascularization and subsequent subretinal fibrosis. Optical coherence tomography(OCT) showed a highly reflective zone in the deeper retina and the choroid. The subretinal fibrosis was mainly located inner to the retinal pigment epithelium.


Copyright © 2006, 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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