Bhavsar Kavita V, Lin Sally, Rahimy Ehsan, Joseph Anthony, Freund K Bailey, Sarraf David, Cunningham Emmett T
Department of Ophthalmology, Vitreous Retina Macula Consultants of New York, Manhattan, New York, USA; Department of Ophthalmology, LuEsther T. Mertz Retinal Research Center, Manhattan Eye, Ear and Throat Hospital, New York, New York, USA; Department of Ophthalmology, New York University Langone Medical Center, New York, New York, USA; Department of Ophthalmology, Columbia University, New York, New York, USA.
Department of Ophthalmology, California Pacific Medical Center, San Francisco, California, USA.
Surv Ophthalmol. 2016 Sep-Oct;61(5):538-65. doi: 10.1016/j.survophthal.2016.03.003. Epub 2016 Mar 10.
Acute macular neuroretinopathy is a relatively rare condition originally defined by the presence of intraretinal, reddish-brown, wedge-shaped lesions, the apices of which tend to point toward the fovea. Acute onset of paracentral scotomas corresponding to the clinically evident lesions is both common and characteristic. Although the pathogenesis of acute macular neuroretinopathy is complex, recent research suggests a microvascular etiology. Advances in multimodal imaging have enabled better characterization of this retinal disorder and have led to newly proposed diagnostic criteria. We review 101 reported cases in the English and non-English language literature identified from 1975, when acute macular neuroretinopathy was first described, to December, 2014. We discuss common risk factors, demographic and clinical characteristics, and multimodal imaging findings, which together provide insights into pathogenesis and guide areas of future investigation.
急性黄斑神经视网膜病变是一种相对罕见的病症,最初定义为存在视网膜内红棕色楔形病变,其尖端往往指向中央凹。与临床上明显病变相对应的旁中心暗点急性发作既常见又具有特征性。尽管急性黄斑神经视网膜病变的发病机制复杂,但最近的研究表明其病因与微血管有关。多模态成像技术的进步使得对这种视网膜疾病有了更好的特征描述,并产生了新提出的诊断标准。我们回顾了1975年(急性黄斑神经视网膜病变首次被描述的年份)至2014年12月期间英文和非英文文献中报道的101例病例。我们讨论了常见的危险因素、人口统计学和临床特征以及多模态成像结果,这些共同为发病机制提供了见解并指导未来的研究方向。