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A case of multifocal posterior pigment epitheliopathy(MPPE)with intraocular inflammation Hidenobu Matsuda 1 , Yasuhiro Sakai 1 , Eriko Ueda 1 , Takeo Fukuchi 1 1Department of Ophthalmology and Visual Science, Niigata University Graduate School of Medical and Dental Science pp.681-687
Published Date 2016/5/15
DOI https://doi.org/10.11477/mf.1410211796
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Abstract Purpose:To report a case of multifocal posterior pigment epitheliopathy(MPPE)with signs of intraocular inflammation.

Case:A 39-year-old male presented with impaired vision in both eyes since 5 days before. He was referred to us with the tentative diagnosis of Vogt-Koyanagi-Harada disease.

Findings:Corrected visual acuity was 0.4 right and 0.6 left. The right eye showed serous retinal detachment in the posterior fundus. The left eye showed exudative lesions and signs of retinal vasculitis all over the fundus. Fluorescein angiography showed dye leakage from the choroid and dye pooling in the subretinal spact in the right eye. The left eye showed dye leakage from retinal vessels. The findings were suggestive of uveitis. Peroral prednisolone at the daily dosis of 30 mg was apparently futile for 2 months. Intravitreal bevacizumab showed no improvement in the left eye. Fundus photocoagulation was applied to exudative lesions after diagnosis of MPPE. Spontaneous improvement set in later. He has been doing well for 3 years until present.

Conclusion:The present case showed findings suggestive of MPPE. The diagnosis was delayed by the presence of retinal vasculitis and by systemic corticosteroid therapy.


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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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