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急性黄斑神经视网膜病变:多模态成像揭示的长期观察结果。

Acute macular neuroretinopathy: long-term insights revealed by multimodal imaging.

机构信息

Department of Ophthalmology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois 60611, USA.

出版信息

Retina. 2012 Sep;32(8):1500-13. doi: 10.1097/IAE.0b013e318263d0c3.

Abstract

PURPOSE

To report the structural and functional changes in acute macular neuroretinopathy (AMN) and their long-term evolution. Multimodal retinal imaging was acquired, including Fourier domain optical coherence tomography (OCT), infrared (IR) reflectance, and near IR autofluorescence (NIA).

METHODS

In this retrospective observational case series, detailed clinical history and multimodal imaging are reported in eight patients with AMN. Manual segmentation of the Fourier domain OCT volume scans was done in one patient with the largest AMN lesion to yield retinal sublayer topographic maps.

RESULTS

Two patients were seen within the first 1 to 2 days of symptoms, and both showed outer nuclear and outer plexiform layer hyperreflectivity. Both patients developed enlargement of the lesion over the first week on IR reflectance imaging with a corresponding lateral extension of the outer retinal disruption on Fourier domain OCT. Thinning of the outer nuclear layer persisted in all patients with lesions >100 μm width, and in one patient this thinning worsened over the course of follow-up, as noted on the sublayer maps. This structural abnormality correlated with long-term functional deficits, persisting up to 14 months after the initial episode. Infrared reflectance highlights the lesion best, and abnormalities on near IR autofluorescence may be present.

CONCLUSION

Acute macular neuroretinopathy acutely affects the outer nuclear and plexiform layers manifesting as OCT hyperreflectivity. The hallmark long-term changes are outer nuclear thinning on Fourier domain OCT and a fading dark lesion on IR reflectance imaging. These changes correspond to focal disruption of the outer segment/retinal pigment epithelium junction on OCT, and not the inner segment/outer segment junction, as previously reported. Optical coherence tomography and near IR autofluorescence abnormalities suggest previously unrecognized melanin and retinal pigment epithelium derangements in this condition.

摘要

目的

报告急性黄斑神经视网膜病变(AMN)的结构和功能变化及其长期演变。采集了多模态视网膜成像,包括傅里叶域光相干断层扫描(OCT)、红外(IR)反射和近红外自发荧光(NIA)。

方法

在这项回顾性观察性病例系列研究中,报告了 8 例 AMN 患者的详细临床病史和多模态成像。对 1 例 AMN 病变最大的患者进行傅里叶域 OCT 容积扫描的手动分割,以获得视网膜亚层地形图。

结果

2 例患者在症状出现后的第 1 至 2 天就诊,均显示外核和外丛状层高反射。两名患者在 IR 反射成像上的病变在第一周内均增大,傅里叶域 OCT 上外视网膜中断也相应地侧向扩展。所有病变宽度>100μm 的患者均持续出现外核层变薄,1 例患者在随访过程中变薄加重,亚层图上可见。这种结构异常与长期功能缺陷相关,在最初发作后长达 14 个月仍存在。IR 反射突出显示病变最佳,近红外自发荧光可能存在异常。

结论

急性黄斑神经视网膜病变急性影响外核和丛状层,表现为 OCT 高反射。长期变化的标志是傅里叶域 OCT 上的外核层变薄和 IR 反射成像上的暗斑消退。这些变化与 OCT 上的外节/视网膜色素上皮连接的局灶性中断相对应,而不是以前报道的内节/外节连接。OCT 和近红外自发荧光异常提示该疾病中以前未被认识到的黑色素和视网膜色素上皮紊乱。

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