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Spectral domain optical coherence tomography in adult-onset vitelliform macular dystrophy with cuticular drusen.

机译:成年发病的玻璃体黄斑营养不良伴表皮玻璃疣的光谱域光学相干断层扫描。

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PURPOSE: The purpose of this study was to investigate morphologic differences in a consecutive case series of patients suffering from adult-onset vitelliform macular dystrophy with cuticular drusen (CD) compared with another patient group with a vitelliform lesion only using high-resolution in vivo retinal imaging. METHODS: Simultaneous spectral domain optical coherence tomography (870 nm, 40.000 A-scans per second) and confocal scanning laser ophthalmoscopy were performed in 6 patients (12 eyes) with adult-onset vitelliform macular dystrophy using a combined instrument (Spectralis HRA+OCT; Heidelberg Engineering, Heidelberg, Germany). RESULTS: Mean age was 69 years (59-82 years), and mean visual acuity was 20/80. The vitelliform lesion presented with an accumulation of yellow-gray material with increased fundus autofluorescence. Spectral domain optical coherence tomography imaging showed that the neurosensory detachment was filled with an amorphous homogenously reflective material located between the retinal pigment epithelium and neurosensory retina in the inferior part of the lesion with the superior part being optically empty. The retinal pigment epithelium basal membrane/Bruch membrane band on spectral domain optical coherence tomography showed multiple focal nodules, in analogy to histologic descriptions of CD. Longitudinal observations in a subgroup of patients showed that the vitelliform detachment collapsed with subsequent development of geographic atrophy in patients with CDs. CONCLUSION: Cuticular drusen may be an indicator for a generalized retinal pigment epithelium dysfunction. High-resolution spectral domain optical coherence tomography allows to image morphologic differences in adult-onset vitelliform macular dystrophy with and without CDs, providing further evidence that adult-onset vitelliform macular dystrophy with CDs represents a separate disease entity.
机译:目的:本研究的目的是调查连续病例组中患有成年性玻璃体黄斑营养不良合并表皮玻璃膜疣(CD)的患者的形态学差异,与仅使用高分辨率体内视网膜的另一例玻璃体病患者的形态学差异成像。方法:使用组合仪器(Spectralis HRA + OCT; Spectralis HRA + OCT;组合仪器)对6例(12眼)成年性玻璃体黄斑营养不良患者进行了同时的光谱域光学相干断层扫描(870 nm,每秒40.000次A扫描)和共聚焦扫描激光眼底镜检查。海德堡工程公司,德国海德堡)。结果:平均年龄为69岁(59-82岁),平均视力为20/80。玻璃体样病变表现为黄灰色物质的积累,眼底自发荧光增加。光谱域光学相干断层扫描成像显示,神经感觉脱离被位于病变下部的视网膜色素上皮和神经感觉视网膜之间的无定形均匀反射材料所充满,而上部则光学上是空的。与CD的组织学描述类似,光谱域光学相干断层扫描上的视网膜色素上皮基底膜/布鲁赫膜带显示出多个局灶结节。在一个患者亚组中的纵向观察显示,玻璃体状脱离随着CD患者的地理萎缩的发展而崩溃。结论:表皮玻璃膜疣可能是广义视网膜色素上皮功能障碍的指标。高分辨率光谱域光学相干断层扫描技术可以在有和没有CD的成年发病的玻璃体黄斑营养不良中对形态学差异进行成像,从而提供进一步的证据表明,成年的有CD的玻璃体黄斑营养不良代表一个独立的疾病实体。

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