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Presumed iris retraction syndrome in a case of rhegmatogenous retinal detachment Fumie Takenobu 1 , Atsushi Yamasaki 1 , Asako Kawaguchi 1 , Yoshifumi Ikeda 1 , Yoshitsugu Inoue 1 , Kazuki Matsuura 2 1Div of Ophthalmol and Vis Sci, Fac of Med, Tottori Univ 2Dept of Ophthalmol, Nojima Hosp pp.1389-1392
Published Date 2012/9/15
DOI https://doi.org/10.11477/mf.1410104367
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Abstract. Purpose:To report a case of rhegmatogenous retinal detachment with suspected iris retraction syndrome. Case:A 59-year-old female presented with pain and impaired vision in her left eye since 3 days before. She had received cataract surgery in the right eye 20 years before. The left eye had been amblyopic since childhood. Findings:Corrected visual acuity was 1.0 right and 0.08 left. Intraocular pressure(IOP)was 14 mmHg right and 7 mmHg left. The left eye showed deep anterior chamber with the iris periphery displaced posteriorly. Echography showed retinal detachment with extensive choroidal detachment in the left eye. Instillation of corticosteroid was followed by relief of pain with IOP rising to 14 mmHg. A horseshoe tear with retinal detachment was found in the upper sector of left fundus. Photocoagulation surrounding the hole was followed by disappearance of retinal and choroidal detachment 7 days after her initial visit. Visual acuity in the left eye improved to 0.6 after cataract surgery. She has been doing well for 5 months until present. Conclusion:This case is suspected of iris retraction syndrome secondary to rhegmatogenous retinal detachment.


Copyright © 2012, 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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