Kishi S, Takahashi H
Department of Ophthalmology, Gunma University School of Medicine, Maebashi, Gunma, Japan.
Am J Ophthalmol. 2000 Jul;130(1):65-75. doi: 10.1016/s0002-9394(00)00383-4.
To describe the morphologic features of idiopathic macular holes and vitreous traction during macular hole evolution.
We prospectively examined 89 eyes of 82 patients with idiopathic macular holes (stage 1, 15 eyes; stage 2, 16 eyes; stage 3, 50 eyes; stage 4, eight eyes) using optical coherence tomography. In addition to optical coherence tomography, scanning laser ophthalmoscopy was performed in all 15 eyes with stage 1 hole, six of 16 eyes with stage 2, and 19 of 50 eyes with stage 3.
In stage 1 eyes, optical coherence tomography revealed retinal split or cystic changes at the fovea in 11 of 15 eyes (73%) and foveal retinal detachment in four eyes (27%). Two eyes with foveal cysts progressed to stage 2, and one developed a stage 3 hole. In one eye with retinal detachment, the detached retina thinned and developed dehiscence. Optical coherence tomography showed a vitreous cortex that was detached in the perifoveal area but attached on the fovea in 11 of the 15 stage 1 eyes. In stage 2 macular holes, retinal tissue extending from the perifoveal retina formed a flap. Scanning laser ophthalmoscopy demonstrated intraretinal radiating striae, which corresponded to a foveal cyst or perifoveal cystic changes.
Macular holes start as retinal splits or foveal cysts in most cases. The anterior wall of the cyst serves as a flap in stage 2 and an operculum in stage 3 holes. Radiating striae correspond to retinal splits or cysts and presumably represent an elevation of Henle fiber. In a few macular holes, foveal detachment is the initial change. The detached retina thins and eventually develops a hole. In both courses, anterior traction of the slightly detached vitreous cortex appears to be a major contributing factor to macular hole formation.
描述特发性黄斑裂孔在其发展过程中的形态学特征以及玻璃体牵引情况。
我们使用光学相干断层扫描技术对82例特发性黄斑裂孔患者的89只眼进行了前瞻性研究(1期,15只眼;2期,16只眼;3期,50只眼;4期,8只眼)。除光学相干断层扫描外,对所有15只1期裂孔眼、16只2期裂孔眼中的6只以及50只3期裂孔眼中的19只进行了扫描激光眼底镜检查。
在1期眼中,光学相干断层扫描显示15只眼中的11只(73%)在黄斑中心凹处有视网膜劈裂或囊性改变,4只眼(27%)有黄斑中心凹视网膜脱离。2只伴有黄斑中心凹囊肿的眼进展为2期,1只发展为3期裂孔。在1只伴有视网膜脱离的眼中,脱离的视网膜变薄并出现裂孔。光学相干断层扫描显示,15只1期眼中的11只在黄斑中心凹周围区域玻璃体皮质脱离,但在黄斑中心凹处附着。在2期黄斑裂孔中,从黄斑中心凹周围视网膜延伸的视网膜组织形成一个瓣片。扫描激光眼底镜检查显示视网膜内放射状条纹,对应于黄斑中心凹囊肿或黄斑中心凹周围囊性改变。
大多数情况下,黄斑裂孔始于视网膜劈裂或黄斑中心凹囊肿。囊肿的前壁在2期作为瓣片,在3期裂孔中作为盖瓣。放射状条纹对应于视网膜劈裂或囊肿,可能代表Henle纤维的隆起。在少数黄斑裂孔中,黄斑中心凹脱离是初始改变。脱离的视网膜变薄,最终形成裂孔。在这两种过程中,轻度脱离的玻璃体皮质的前部牵引似乎是黄斑裂孔形成的主要促成因素。