Histopathologic study of presumed parafoveal telangiectasis

被引:35
作者
Eliassi-Rad, B
Green, WR
机构
[1] Wilmer Ophthalmol Inst, Eye Pathol Lab, Baltimore, MD USA
[2] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
来源
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES | 1999年 / 19卷 / 04期
关键词
histopathologic study; parafoveal telangiectasis; retinal-choroid anastomosis; retinal neovascularization; retinal pigment epithelial hyperplasia;
D O I
10.1097/00006982-199907000-00011
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To report the postmortem histopathologic features that closely resemble the clinical features of parafoveal telangiectasis. Methods: Light and electron microscopy. Results: Histopathologic features included macular edema; telangiectatic vessels; retinal, subretinal, and superficial retinal neovascularization; retinal pigment epithelial hyperplasia around neovascular aggregates; retinal-choroidal vascular anastomosis; and superficial pigmented cells with lipofuscin. Conclusion: The postmortem histopathologic findings in a 36-year-old woman with Down syndrome and other systemic conditions correlate with features noted in previous reports of presumed parafoveal telangiectasis.
引用
收藏
页码:332 / 335
页数:4
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