Lee Kyoung Min, Woo Se Joon, Hwang Jeong-Min
Department of Ophthalmology, Seoul National University College of Medicine, Seoul, South Korea.
Graefes Arch Clin Exp Ophthalmol. 2014 Nov;252(11):1853-60. doi: 10.1007/s00417-014-2680-9. Epub 2014 Jun 7.
To investigate the anatomic characteristics of congenital excavated optic disc anomalies by using fundus photography, spectral-domain optical coherence tomography (SD-OCT), and swept-source optical coherence tomography (SS-OCT).
Fourteen eyes from 13 patients with congenital excavated optic disc anomalies underwent a complete ophthalmologic examination that included best-corrected visual acuity evaluation, fundus photography, and SD-OCT. SS-OCT was performed in cases of peripapillary staphyloma cases in which the excavation depth could not be detected with SD-OCT. On the basis of the funduscopic and OCT findings, patients were classified as morning glory syndrome, optic disc coloboma, or peripapillary staphyloma.
Seven eyes with morning glory syndrome were characterized by the presence of the preretinal tractional membrane in front of the excavated optic disc and could be divided into two groups: three eyes without retinal excavation, and four eyes with retinal excavation. Four eyes with optic disc coloboma showed inferiorly decentered scleral excavations with shallow optic disc excavation detectable by SD-OCT. Three eyes with peripapillary staphyloma showed deep excavation, the depth of which could not be detected by SD-OCT. SS-OCT and enhanced depth imaging SD-OCT images focused on the bottom revealed membranous structure at the bottom of the excavation in two cases with peripapillary staphyloma.
SD-OCT and SS-OCT are helpful for differential diagnosis of excavated optic disc anomalies. Morning glory syndrome, optic disc coloboma, and peripapillary staphyloma were respectively characterized by the presence of a preretinal tractional membrane, inferiorly decentered excavation, and an excavation deeper than that observed in morning glory syndrome and optic disc coloboma.
通过眼底照相、频域光学相干断层扫描(SD-OCT)和扫频光学相干断层扫描(SS-OCT)研究先天性视盘凹陷异常的解剖特征。
对13例患有先天性视盘凹陷异常的患者的14只眼进行了全面的眼科检查,包括最佳矫正视力评估、眼底照相和SD-OCT。对于SD-OCT无法检测到凹陷深度的视乳头周围葡萄肿病例,进行了SS-OCT检查。根据眼底镜和OCT检查结果,将患者分为牵牛花综合征、视盘缺损或视乳头周围葡萄肿。
7只患有牵牛花综合征的眼睛的特征是在凹陷的视盘前方存在视网膜前牵引膜,可分为两组:3只无视网膜凹陷的眼睛和4只伴有视网膜凹陷的眼睛。4只患有视盘缺损的眼睛表现为巩膜凹陷向下移位,SD-OCT可检测到浅的视盘凹陷。3只患有视乳头周围葡萄肿的眼睛表现为深度凹陷,SD-OCT无法检测到其深度。SS-OCT和增强深度成像SD-OCT图像聚焦于底部,在2例视乳头周围葡萄肿病例中显示凹陷底部有膜状结构。
SD-OCT和SS-OCT有助于视盘凹陷异常的鉴别诊断。牵牛花综合征、视盘缺损和视乳头周围葡萄肿分别以视网膜前牵引膜的存在、凹陷向下移位和比牵牛花综合征及视盘缺损更深的凹陷为特征。