Uemura Akinori, Otsuji Futoshi, Nakano Tetsuro, Sakamoto Taiji
*Department of Ophthalmology, Kagoshima City Hospital, Kagoshima, Japan; and †Department of Ophthalmology, Kagoshima University Graduate School of Medicine and Dental Sciences, Kagoshima, Japan.
Retina. 2014 Jun;34(6):1229-34. doi: 10.1097/IAE.0000000000000046.
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.
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.
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.
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.
研究单侧黄斑裂孔患者健眼中玻璃体黄斑界面与光感受器微结构完整性之间的关系。
回顾性观察病例系列。本研究纳入了55例单侧黄斑裂孔患者的55只健眼。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结果对玻璃体黄斑界面的特征进行分级。
初诊时,55只眼中有28只(51%)存在玻璃体黄斑附着,伴或不伴有黄斑中心凹周围玻璃体后脱离。初诊时,在18只黄斑中心凹周围玻璃体后脱离且所有象限均与黄斑中心凹持续附着的眼中,有11只(61%)观察到圆锥外段顶端线呈三角形抬高。相反,其余37只处于其他玻璃体后脱离阶段的眼睛均未显示任何异常。在平均18个月(范围12 - 24个月)的随访期内,3只眼在玻璃体黄斑自发分离且未形成黄斑裂孔后,圆锥外段顶端线的抬高消失;6只眼保持不变;2只眼进展为全层黄斑裂孔。
这些发现表明,黄斑裂孔患者健眼中圆锥外段顶端线的抬高是由玻璃体在黄斑中心凹处的局部牵引所致。这被认为是全层黄斑裂孔形成过程中在黄斑组织中观察到的重要原发性改变。