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Vitreomacular interface and outer foveal microstructure in fellow eyes of patients with unilateral macular holes

机译:单侧黄斑裂孔患者同侧眼玻璃体界面和中央凹外微结构

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PURPOSE:: To investigate the relationship between the vitreomacular interface and the integrity of the photoreceptor microstructures in the normal fellow eyes of patients with unilateral macular holes. METHODS:: Retrospective observational case series. Fifty-five normal fellow eyes of 55 patients with unilateral macular holes were enrolled in the study. All patients underwent complete ophthalmologic examination including best-corrected visual acuity, slit-lamp biomicroscopy, fundus photography, and spectral domain optical coherence tomography at initial and follow-up visits. The features of the vitreomacular interface were graded based on spectral domain optical coherence tomography findings. RESULTS:: At the initial visit, 28 of 55 eyes (51%) had vitreomacular attachments with or without perifoveal posterior vitreous detachment. On their initial visit, a triangular elevation of the cone outer segment tips line was identified in 11 of 18 eyes (61%) with perifoveal posterior vitreous detachment across all quadrants with persistent attachment to the fovea. Conversely, none of the remaining 37 eyes with the other stages of posterior vitreous detachment showed any abnormalities. Over a mean follow-up period of 18 months (range, 12-24 months), the elevation of the cone outer segment tips line resolved after spontaneous vitreomacular separation without macular holes in 3 eyes, remained unchanged in 6 eyes, and showed progression to a full-thickness macular hole in 2 eyes. CONCLUSION:: These findings suggest that an elevation of the cone outer segment tips line in the normal fellow eyes of patients with macular holes is caused by the focal traction of the vitreous at the foveal center. This is considered to be an important primary change observed in the macular tissue in full-thickness macular hole formation.
机译:目的:研究玻璃体界面与单侧黄斑裂孔患者正常同侧眼睛的感光细胞微结构完整性之间的关系。方法::回顾性观察病例系列。研究纳入了55例单侧黄斑裂孔患者的55只正常同眼。所有患者在初诊和随访时均接受了全面的眼科检查,包括最佳矫正视力,裂隙灯生物显微镜检查,眼底照相和光谱域光学相干断层扫描。根据光谱域光学相干断层扫描的发现,对玻璃体界面的特征进行了分级。结果:在初次就诊时,在55眼中有28眼(51%)具有玻璃体附件,伴或不伴有中央凹后玻璃体脱离。初次访视时,在18眼中有11眼(61%)中发现圆锥形外段尖端线呈三角形升高,所有象限均伴有中央凹后玻璃体脱离,并持续附着于中央凹。相反,其余37眼具有玻璃体后脱离其他阶段的眼睛均未显示任何异常。在平均随访期18个月(范围12-24个月)中,自发性玻璃体分离后3眼无黄斑裂孔的锥体外段尖端线的升高得到了解决,6眼保持不变,并且进展为2只眼睛有一个全层的黄斑裂孔。结论:这些发现表明,黄斑裂孔患者正常同侧视锥外段尖端线的升高是由玻璃体在中央凹中心的局灶性牵引引起的。这被认为是在全厚度黄斑裂孔形成中在黄斑组织中观察到的重要的主要变化。

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