LuEsther T Mertz Retinal Research Center, Manhattan Eye, Ear, and Throat Hospital, New York, New York, USA.
Ophthalmology. 2010 Feb;117(2):303-12.e1. doi: 10.1016/j.ophtha.2009.07.014. Epub 2009 Oct 7.
To characterize reticular pseudodrusen, a potential risk factor for late age-related macular degeneration.
Retrospective, observational case series.
Fifty-eight eyes of 33 patients with pseudodrusen (20 female).
Consecutive patients with reticular pseudodrusen, diagnosed by their typical appearance and distribution using ophthalmoscopy, the blue channel of color fundus photographs, and near infrared images. The patients were imaged by spectral domain optical coherence tomography (SD OCT), and correlations were made between the near infrared images and the SD OCT images. The SD OCT findings in patients with pseudodrusen were compared with previously reported histologic findings of subretinal drusenoid deposits. The histologic specimens were reevaluated with the additional knowledge of the clinical information.
Spectral domain optical coherence tomography and histologic characteristics of pseudodrusen.
The mean age of the 33 patients was 81.7 years. The correlating SD OCT scans showed collections of granular hyperreflective material above the retinal pigment epithelium (RPE), in the subretinal space located primarily between the RPE and the boundary between the inner and outer segments of the photoreceptors (IS/OS boundary). In a more advanced stage, this material formed small mounds that broke through the IS/OS boundary. There were no correlates to the deposits seen under the RPE or in the choroid. These findings were similar in character to previously reported histologic characterization of subretinal drusenoid deposits, which had identified the presence of membranous debris, unesterified cholesterol, and complement within the deposits.
Pseudodrusen seen by clinical examination may be subretinal drusenoid deposits seen by histologic examination. This unexpected location suggests that potential pathophysiologic mechanisms on both sides of the RPE need to be taken into account in theories related to the development of age-related macular degeneration.
描述可能导致晚期年龄相关性黄斑变性的网状假性玻璃膜疣。
回顾性观察性病例系列。
33 名患者的 58 只眼有假性玻璃膜疣(20 名女性)。
连续的患有网状假性玻璃膜疣的患者,通过眼科检查、眼底彩照的蓝色通道和近红外图像的典型外观和分布进行诊断。对患者进行频域光学相干断层扫描(SD-OCT)成像,并对近红外图像和 SD-OCT 图像进行相关性分析。将假性玻璃膜疣患者的 SD-OCT 结果与先前报道的视网膜下类 drusen 沉积物的组织学发现进行比较。在具有临床信息的附加知识的情况下,重新评估组织学标本。
SD-OCT 和假性玻璃膜疣的组织学特征。
33 名患者的平均年龄为 81.7 岁。相关的 SD-OCT 扫描显示,视网膜色素上皮(RPE)上方的视网膜下空间存在颗粒状高反射物质的集合,主要位于 RPE 和光感受器内外节(IS/OS 边界)之间。在更晚期,该物质形成小丘,突破 IS/OS 边界。在 RPE 下方或脉络膜中没有与沉积物相关的物质。这些发现与先前报道的视网膜下类 drusen 沉积物的组织学特征相似,这些沉积物中已确定存在膜状碎片、未酯化胆固醇和补体。
临床检查中所见的假性玻璃膜疣可能是组织学检查中所见的视网膜下类 drusen 沉积物。这种出乎意料的位置表明,在与年龄相关性黄斑变性发展相关的理论中,需要考虑 RPE 两侧的潜在病理生理机制。