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Japanese

Intravitreal granulation and retinal pigment epitheliopathy in Behçet's disease Shoji Kishi 1 , Shin Yoneya 1 , Naoto Ohnishi 1 , Tomomitsu Horiuchi 1 1Department of Ophthalmology, Gunma University School of Medicine pp.1139-1148
Published Date 1981/7/15
DOI https://doi.org/10.11477/mf.1410208396
  • Abstract
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We examined 5 eyes in the terminal stage of Behçet's disease by histological and electron micro-scopic means. Granulation tissue filled the vitre-ous cavity completely in each of the five eyes. We paid particular attention to the elucidation of the origin and the progression of granulation formation.

The granule tissue originated from the uvea through denuded retinal pigment epithelium (RPE) at the vitreous base, the anterior iris sur-face and the chamber angle. When the RPE still retained its continuity, fibroblasts could not invade the vitreous cavity from the choroid.


Copyright © 1981, 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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