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A case of lattice corneal dystrophy associated with spheroidal keratopathy Noriaki Yamamoto 1 , Satoshi Kimura 2 , Koji Hirano 2 , Tetsuro Nagasaka 3 , Miya Kobayashi 4 1Dept of Ophthalmol, Gamagori City Hosp 2Dept of Ophthalmol, Nagoya Univ Sch of Med 3Dev of Pathol, Cli lab, Nagoya Univ Hosp 42nd Dept of Anatomy, Nagoya Univ Sch of Med pp.1571-1574
Published Date 1997/9/15
DOI https://doi.org/10.11477/mf.1410905549
  • Abstract
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We diagnosed a 65-year-old female as type I lattice corneal dystrophy. Slitlamp biomicroscopy showed globular and ambercolored deposits beneath the epithelium with stromal opacity consistent with lattice dystrophy in both eyes. Deep lamellar keratoplasty was performed on both eyes. Histopathological studies showed characteristic features of spheroidal keratopathy and amyloid dystrophy. No complications has developed during 2 years after keratoplasty. To the best of our knowledge, this is the first reported case of lattice corneal dystrophy associated with spheroidal keratopathy in Japan.


Copyright © 1997, 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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