Lee Sun Young, Cheng Justine L, Gehrs Karen M, Folk James C, Sohn Elliott H, Russell Stephen R, Guo Zhihui, Abràmoff Michael D, Han Ian C
Department of Ophthalmology and Visual Sciences, Carver College of Medicine, University of Iowa, Iowa City.
Carver College of Medicine, University of Iowa, Iowa City.
JAMA Ophthalmol. 2017 Nov 1;135(11):1177-1183. doi: 10.1001/jamaophthalmol.2017.3790.
Acute macular neuroretinopathy (AMN) is a rare, idiopathic condition resembling other acute maculopathies such as paracentral acute middle maculopathy. The pathophysiology of AMN is not well understood, and the role of the choroid in the pathogenesis of AMN remains controversial.
To describe initial and serial multimodal imaging findings in AMN, with attention to choroidal vascular changes.
DESIGN, SETTING, AND PARTICIPANTS: Retrospective case series at a single institution, tertiary referral center. The case series included 7 patients with clinical diagnosis of AMN.
Multimodal imaging findings, including fundus photography, fluorescein angiography, spectral-domain optical coherence tomography (OCT), en face near-infrared imaging, fundus autofluorescence, optical coherence tomography angiography (OCTA), and automated quantification of the regional structural context of choroidal flow interest between different imaging modalities, using an automatic algorithm.
Nine eyes from 7 patients (5 women and 2 men; mean age, 40.1 years) with a diagnosis of AMN were included. Mean duration of follow-up was 11 weeks (range, 1-25 weeks). All eyes had inner choroidal flow void on OCTA that topographically corresponded to regions of abnormal hyperreflectance of the outer retinal layers on spectral-domain OCT and hyporeflectance on en face near-infrared imaging (dice similarity coefficient, 0.76). For each patient, these areas of choroidal flow void on OCTA persisted during the follow-up period, while the abnormal hyperreflectance of outer plexiform layer and inner nuclear layer on spectral-domain OCT was observed to improve.
These findings suggest that areas of inner choroidal vascular flow void on OCTA are seen in patients with AMN. These areas may persist weeks after the onset of symptoms and suggest that vascular compromise of the inner choroid may be involved in the pathogenesis of AMN.
急性黄斑神经视网膜病变(AMN)是一种罕见的特发性疾病,类似于其他急性黄斑病变,如中心旁急性中黄斑病变。AMN的病理生理学尚未完全了解,脉络膜在AMN发病机制中的作用仍存在争议。
描述AMN的初始和系列多模态成像结果,重点关注脉络膜血管变化。
设计、地点和参与者:在一家三级转诊中心的单一机构进行的回顾性病例系列研究。该病例系列包括7例临床诊断为AMN的患者。
多模态成像结果,包括眼底照相、荧光素血管造影、光谱域光学相干断层扫描(OCT)、正面近红外成像、眼底自发荧光、光学相干断层扫描血管造影(OCTA),以及使用自动算法对不同成像方式之间脉络膜血流感兴趣区域的区域结构背景进行自动量化。
纳入了7例诊断为AMN的患者的9只眼(5名女性和2名男性;平均年龄40.1岁)。平均随访时间为11周(范围1 - 25周)。所有眼睛在OCTA上均有脉络膜内层血流缺失,其在地形上与光谱域OCT上视网膜外层异常高反射区域以及正面近红外成像上的低反射区域相对应(骰子相似系数为0.76)。对于每位患者,OCTA上这些脉络膜血流缺失区域在随访期间持续存在,而光谱域OCT上外丛状层和内核层的异常高反射则有所改善。
这些发现表明,AMN患者在OCTA上可见脉络膜内层血管血流缺失区域。这些区域可能在症状出现数周后持续存在,提示脉络膜内层的血管损害可能参与了AMN的发病机制。