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黄斑裂孔发育阶段的生物显微镜分类再评估。

Reappraisal of biomicroscopic classification of stages of development of a macular hole.

作者信息

Gass J D

机构信息

Bascom Palmer Eye Institute, Department of Ophthalmology, University of Miami Medical Center, Florida, USA.

出版信息

Am J Ophthalmol. 1995 Jun;119(6):752-9. doi: 10.1016/s0002-9394(14)72781-3.

Abstract

PURPOSE

To update the biomicroscopic classification and anatomic interpretations of the stages of development of age-related macular hole and provide explanations for the remarkable recovery of visual acuity that occurs in some patients after vitreous surgery.

METHODS

Recent biomicroscopic observations of various stages of macular holes are used to postulate new anatomic explanations for these stages.

RESULTS

Biomicroscopic observations include the following: (1) the change from a yellow spot (stage 1-A) to a yellow ring (stage 1-B) during the early stages of foveal detachment is unique to patients at risk of macular hole; (2) the prehole opacity with a small stage 2 hole may be larger than the hole diameter; and (3) the opacity resembling an operculum that accompanies macular holes is indistinguishable from a pseudo-operculum found in otherwise normal fellow eyes.

CONCLUSIONS

The change from a yellow spot (stage 1-A) to a yellow ring (stage 1-B) is caused primarily by centrifugal displacement of retinal receptors after a dehiscence at the umbo. The hole may be hidden by semiopaque contracted prefoveolar vitreous cortex bridging the yellow ring (stage 1-B occult hole). Stage 1-B occult holes become manifest (stage 2 holes) either after early separation of the contracted prefoveolar vitreous cortex from the retina surrounding a small hole or as an eccentric can-opener-like tear in the contracted prefoveolar vitreous cortex, at the edge of larger stage 2 holes. Most prehole opacities probably contain no retinal receptors (pseudo-opercula). Surgical reattachment of the retina surrounding the hole and centripetal movement of the foveolar retina induced by gliosis may restore foveal anatomy and function to near normal.

摘要

目的

更新年龄相关性黄斑裂孔发育阶段的生物显微镜分类及解剖学解释,并为玻璃体手术后部分患者视力显著恢复提供解释。

方法

利用近期对黄斑裂孔各阶段的生物显微镜观察结果,对这些阶段提出新的解剖学解释。

结果

生物显微镜观察结果如下:(1)黄斑裂孔高危患者在黄斑中心凹脱离早期,从黄斑(1-A期)变为黄环(1-B期)的变化具有独特性;(2)2期小孔前的孔前混浊可能大于孔直径;(3)与黄斑裂孔相伴的类似盖膜的混浊与在正常对侧眼中发现的假盖膜难以区分。

结论

从黄斑(1-A期)变为黄环(1-B期)主要是由于中心凹处裂开后视网膜感受器的离心移位所致。裂孔可能被桥接黄环的半透明收缩的黄斑前玻璃体皮质遮挡(1-B期隐匿性裂孔)。1-B期隐匿性裂孔在收缩的黄斑前玻璃体皮质与小孔周围视网膜早期分离后,或在较大2期裂孔边缘的收缩的黄斑前玻璃体皮质出现类似开罐器样的偏心撕裂时,变为明显的(2期裂孔)。大多数孔前混浊可能不包含视网膜感受器(假盖膜)。裂孔周围视网膜的手术复位以及胶质增生引起的黄斑中心凹视网膜向心运动可能使黄斑的解剖结构和功能恢复至接近正常。

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