Wong Wai T, Forooghian Farzin, Majumdar Zigurts, Bonner Robert F, Cunningham Denise, Chew Emily Y
Office of the Scientific Director, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.
Am J Ophthalmol. 2009 Oct;148(4):573-83. doi: 10.1016/j.ajo.2009.04.030. Epub 2009 Jul 2.
To use multiple imaging methods to investigate patients with type 2 idiopathic macular telangiectasia (IMT) at different disease severity stages so as to characterize and categorize disease progression through the full spectrum of disease phenotypes.
Observational case series.
Twelve patients with type 2 IMT (22 eyes) examined with fundus photography, angiography, optical coherence tomography imaging, fundus autofluorescence (FAF), and microperimetry testing in an institutional setting.
Eyes examined by multiple imaging methods were classified into 5 proposed categories (0 through 4): category 0 (fellow) eyes had normal results on all imaging methods. Category 1 eyes had increased foveal autofluorescence on FAF imaging as the only imaging abnormality. Category 2 eyes had increased foveal autofluorescence together with funduscopic and angiographic features typical of type 2 IMT. Category 3 eyes had additional evidence of foveal atrophy on optical coherence tomography, and category 4 eyes had all the above features plus clinically evident pigment clumping. FAF signal increased in intensity in the foveal region from category 0 through category 3, whereas category 4 eyes demonstrated a mixed pattern of increased and decreased FAF signal.
The findings here outline a sequence of progressive changes seen with multiple imaging methods in advancing stages of disease. Increase in foveal autofluorescence is an early anatomic change in type 2 IMT that may precede typical clinical and angiographic changes. Loss of macular pigment density in the fovea and a changing composition of fluorophores in the retinal pigment epithelium may underlie these changes on FAF in the fundus.
运用多种成像方法对不同疾病严重程度阶段的2型特发性黄斑毛细血管扩张症(IMT)患者进行研究,以通过疾病表型的全谱来描述和分类疾病进展。
观察性病例系列。
在机构环境中,对12例2型IMT患者(22只眼)进行眼底照相、血管造影、光学相干断层扫描成像、眼底自发荧光(FAF)和微视野测试。
通过多种成像方法检查的眼睛被分为5个提议的类别(0至4):0类(对侧)眼在所有成像方法上结果均正常。1类眼在FAF成像上仅表现为中心凹自发荧光增加这一成像异常。2类眼中心凹自发荧光增加,同时伴有2型IMT典型的眼底和血管造影特征。3类眼在光学相干断层扫描上有中心凹萎缩的额外证据,4类眼具有上述所有特征以及临床上明显的色素沉着。从0类到3类,中心凹区域的FAF信号强度增加,而4类眼表现出FAF信号增加和减少的混合模式。
此处的研究结果概述了在疾病进展阶段通过多种成像方法观察到的一系列渐进性变化。中心凹自发荧光增加是2型IMT的早期解剖学变化,可能先于典型的临床和血管造影变化。黄斑中心凹色素密度降低以及视网膜色素上皮中荧光团组成的变化可能是眼底FAF上这些变化的基础。