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Two cases of acute posterior multifocal placoid pigment epitheliopathy (APMPPE) Mitsuko Yuzawa 1 1Dept. of Ophthalmol, Sch of Med, Nihon Univ pp.1327-1332
Published Date 1986/12/15
DOI https://doi.org/10.11477/mf.1410209907
  • Abstract
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Two cases of acute posterior multifocal placoid pig-ment epitheliopathy (APMPPE), seen in females aged 49 and 56 years, showed peculiar features suggestive ofpossible pathogenesis of this disease.

The first case showed persistent small hypofluores-cent areas in the fluorescent angiogram in the apparent-ly healthy fellow eye. Two weeks later, this eye manifested signs of APMPPE. It appeared that persis-tent circulatory disturbances in the choriocapillaris led to barrier dysfunction of the RPE and then to the development of placoid lesions.

The second case developed localized serous detach-ments in the yellowish lesions during the long course of recurrences of this diseases. Late-phase angiograms showed intense dye leakage in the yellowish lesions.

The serous detachment of the sensory retina was appar-ently consequent to the barrier dysfunction of the RPE as located in the yellowish lesions.

Rinsho Ganka (Jpn J Clin Ophthalmo0 40(12) : 1327-1332, 1986


Copyright © 1986, 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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