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Treatment and hematological features of Eales's disease Keiko Sato 1 , Kunihiko Shiraki 1 , Kazunori Inoue 1 , Tokuhiko Miki 1 , Yoichi Tatsumi 2 1Dep. of Ophthalmol., Osaka City Univ. Sch. of Med. 2Dept. of Lab. Med., Osaka City Univ. Sch. of Med pp.322-329
Published Date 1985/3/15
DOI https://doi.org/10.11477/mf.1410209365
  • Abstract
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We evaluated 34 cases with peripheral retinal neovascularization diagnosed as Eales's disease. Argon laser photocoagulation was performed in 32 eyes (23 cases) and vitrectomy in 4 eyes (4 cases). No recurrent vitreous hemorrhage occurred in these treated eyes. The favorable prognosis was due to early detection of vascular abnormalities in the peripheral retina and sufficient argon laser photo-coagulation to nonperfused areas observed by re-peated fluorescein angiography. In some cases, neovascularization persisted after repeated photo-coagulation to the nonperfused areas. Direct photo-coagulation was applied to these persistent newly formed vessels. Hematological studies showed normal levels of fibrinopeptide A. An increased level of fibrinopeptide Bβ 15-42 was observed in some cases. This feature seemed to be possibly related to the pathogenesis of Eales's disease.


Copyright © 1985, 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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