Ultrastructural and clinical evidence of subretinal debris accumulation in type 2 macular telangiectasia

被引:22
作者
Cherepanoff, Svetlana [2 ,3 ]
Killingsworth, Murray C. [3 ,4 ]
Zhu, Meidong [1 ]
Nolan, Timothy [5 ,6 ]
Hunyor, Alex P. [1 ,7 ]
Young, Stephanie H. [8 ]
Hageman, Gregory S. [9 ]
Gillies, Mark C. [1 ,7 ]
机构
[1] Univ Sydney, Save Sight Inst, Sydney, NSW 2006, Australia
[2] Prince Wales Hosp, SEALS, Randwick, NSW 2031, Australia
[3] Univ NSW, Fac Med, Randwick, NSW, Australia
[4] Liverpool Hosp, SWAPS, Liverpool, NSW, Australia
[5] St Vincents Hosp, Darlinghurst, NSW 2010, Australia
[6] Bankstown Hosp, Bankstown, NSW, Australia
[7] Retina Associates, Chatswood, NSW, Australia
[8] Repatriat Gen Hosp, Concord, NSW, Australia
[9] Univ Utah, John A Moran Ctr, Dept Ophthalmol, Salt Lake City, UT USA
关键词
JUXTAFOVEOLAR RETINAL TELANGIECTASIS; DEGENERATION; INJURY;
D O I
10.1136/bjophthalmol-2011-301009
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Aims To describe subretinal debris found on ultrastructural examination in an eye with macular telangiectasia (MacTel) type 2 and on optical coherence tomography (OCT) in a subset of patients with MacTel type 2. Methods Blocks from the mid-periphery and temporal perifovea of an eye with clinically documented MacTel type 2 were examined with electron microscopy (EM). Cases came from the Sydney centre of the MacTel project and the practices of the authors. Results On EM examination, subretinal debris was found in the perifovea with accumulation of degenerate photoreceptor elements in the subretinal space. Despite the substantial subretinal debris, there was minimal retinal pigment epithelial (RPE) reaction. Focal defects were seen in the inner limiting membrane in the perifovea. Of the 65 Sydney MacTel project participants, three (5%) had prominent yellow material at the fovea. OCT revealed smooth mounds between the RPE and the ellipsoid region. The material was hyperautofluorescent. Conclusions This study suggests that subretinal accumulation of photoreceptor debris may be a feature of MacTel type 2. Ultrastructural and OCT evidence of disease beyond the vasculature, involving photoreceptors and Muller cells, is presented.
引用
收藏
页码:1404 / 1409
页数:6
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