Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, Tokyo, Japan.
Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, Tokyo, Japan.
Ophthalmol Retina. 2021 Jul;5(7):702-710. doi: 10.1016/j.oret.2020.10.012. Epub 2020 Oct 28.
To describe the vitreoretinal structure at the margin of the choroidal coloboma in infants and older patients using swept-source (SS) OCT.
Retrospective case series.
Nineteen eyes of 16 patients with choroidal coloboma (7 males, 9 females; average age, 12.3 ± 7.1 years).
The patients were classified into 2 groups: infants 1 year of age or younger (3 eyes) and older patients (16 eyes). Each finding on SS OCT was documented according to previously defined histopathologic findings.
Description of the SS OCT features of choroidal colobomas.
Swept-source OCT showed that the extracolobomatous retina centrally traversed the margin to continue as the marginal intercalary membrane (MICM), whereas the outer layers of the MICM were reversed at the point (point of reversal [POR]). The expected duplication was seen in all infant eyes, but in none of the older eyes whose outer layers of the MICM were ambiguous. However, at the boundary between the layered MICM and monolayered central intercalary membrane (CICM), the POR was detectable in all patients. Further SS OCT analysis showed that the MICM schisis and CICM schisis occurred simultaneously with vitreous traction. Retinal detachments (RDs) seen in 4 eyes were connected to the only MICM schisis, and a MICM break was identified in 1 eye. Swept-source OCT showed that retinal pigment epithelial hyperplasia adhered tightly to the retina and that the glial triangle was adhered tightly to the sclera, indicating barriers to the development of RD after MICM schisis.
Swept-source OCT first visualized the POR in infant eyes and showed that the POR was identifiable despite the atrophic changes in the outer layer of the MICM in the older eyes. Based on the POR location, we confirmed that the intercalary membranes reported in previous OCT studies were clearly differentiated between the MICM and CICM. We also showed that the presence of MICM and CICM schisis resulted from vitreous traction at the coloboma margin and that MICM breaks induced RD only if the barrier that prevented the development of RD was broken.
使用扫频源(SS)OCT 描述脉络膜缺损边缘的视网膜脉络膜结构。
回顾性病例系列。
16 例脉络膜缺损患者的 19 只眼(7 名男性,9 名女性;平均年龄 12.3±7.1 岁)。
将患者分为 2 组:1 岁或 1 岁以下的婴儿(3 只眼)和年龄较大的患者(16 只眼)。根据先前定义的组织病理学发现,记录 SS OCT 上的每个发现。
脉络膜缺损的 SS OCT 特征描述。
SS OCT 显示,中央的额外视网膜穿过边缘继续作为边缘间插膜(MICM),而 MICM 的外层层在点(反转点[POR])反转。所有婴儿眼中均可见预期的重复,但在外层 MICM 不确定的年龄较大的眼中均未见。然而,在分层 MICM 和单层中央间插膜(CICM)之间的边界处,所有患者均可检测到 POR。进一步的 SS OCT 分析显示,MICM 分裂和 CICM 分裂与玻璃体牵引同时发生。4 只眼中的视网膜脱离(RD)与唯一的 MICM 分裂有关,1 只眼中发现 MICM 断裂。SS OCT 显示视网膜色素上皮增生紧密附着于视网膜,神经胶质三角紧密附着于巩膜,表明 MICM 分裂后 RD 不易发展。
SS OCT 首次在婴儿眼中可视化 POR,并显示尽管年龄较大的眼中 MICM 外层层萎缩,但 POR 仍可识别。根据 POR 的位置,我们证实了先前 OCT 研究中报告的间插膜在 MICM 和 CICM 之间明显区分。我们还表明,MICM 和 CICM 分裂的存在是由于脉络膜缺损边缘的玻璃体牵引所致,只有当阻止 RD 发展的屏障被打破时,MICM 断裂才会导致 RD。