Charbel Issa P, Heeren T F C, Krüger E, Zeimer M, Pauleikhoff D, Holz F G
Universitäts-Augenklinik Bonn, Ernst-Abbe-Str. 2, 53127, Bonn, Deutschland,
Ophthalmologe. 2014 Sep;111(9):819-28. doi: 10.1007/s00347-014-3082-4.
Macular telangiectasia type 2 is characterized by atrophic alterations of the central retina which is accompanied by a defined vascular phenotype. The disease manifests within an oval central retinal area the size of approximately two disc diameters, with a topographic predisposition temporal to the foveal center. Funduscopy reveals reduced retinal transparency, crystalline deposits, mildly ectatic capillaries, thickened venules and retinal pigment plaques. Secondary neovascularization and macular holes may occur during the disease course. Fluorescein angiography usually shows a diffuse leakage and often ectatic capillaries. On optical coherence tomography (OCT) examination, hyporeflective cavities and focal atrophy of the photoreceptor layer represent a frequent finding. A characteristic sign is an increased (para) central signal on fundus autofluorescence imaging due to a reduced density of macular pigment.
2型黄斑毛细血管扩张症的特征是中央视网膜出现萎缩性改变,并伴有特定的血管表型。该疾病表现在一个椭圆形的中央视网膜区域,大小约为两个视盘直径,在黄斑中心颞侧具有地形易感性。眼底检查显示视网膜透明度降低、结晶样沉积物、轻度扩张的毛细血管、增粗的小静脉和视网膜色素斑。疾病过程中可能会出现继发性新生血管形成和黄斑裂孔。荧光素血管造影通常显示弥漫性渗漏,且常伴有扩张的毛细血管。在光学相干断层扫描(OCT)检查中,低反射腔和光感受器层的局灶性萎缩是常见表现。一个特征性体征是由于黄斑色素密度降低,眼底自发荧光成像上中央(旁)信号增强。