Sacconi Riccardo, Freund K Bailey, Yannuzzi Lawrence A, Dolz-Marco Rosa, Souied Eric, Capuano Vittorio, Semoun Oudy, Phasukkijwatana Nopasak, Sarraf David, Carnevali Adriano, Querques Lea, Bandello Francesco, Querques Giuseppe
Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele, Milan, Italy.
Vitreous Retina Macula Consultants of New York, New York, New York.
Am J Ophthalmol. 2017 Dec;184:137-146. doi: 10.1016/j.ajo.2017.10.009. Epub 2017 Oct 27.
To expand our understanding of the uncommon entity, referred to as perifoveal exudative vascular anomalous complex (PEVAC) by describing multimodal imaging findings, including optical coherence tomography angiography (OCT-A).
Retrospective cohort study.
Patients diagnosed with PEVAC were identified at 4 retina referral centers worldwide and underwent complete ophthalmologic examination including structural OCT, OCT-A, fluorescein angiography (FA), and indocyanine green angiography (ICGA). Demographics and clinical findings were analyzed at baseline and at available follow-ups.
Fifteen eyes (15 patients, mean age 73 ± 13 years) were included. Six of 15 eyes were diagnosed with coincident age-related macular degeneration (AMD) and 2 with myopic macular degeneration. On fundus examination PEVAC presented as a large perifoveal isolated aneurysm, unifocal in 12 of 15 eyes, associated with small retinal hemorrhages and intraretinal exudation. On structural OCT, PEVAC appeared as a round hyperreflective lesion with hyporeflective lumen, typically surrounded by intraretinal cystic spaces. Dye angiography demonstrated a well-defined hyperfluorescent lesion with variable leakage on FA and without leakage on ICGA. OCT-A showed flow signal correlating with the aneurysmal lesion connecting to retinal capillary plexuses. Seven patients were followed for 13.0 ± 10.5 months with no evidence of functional/anatomic changes. Three patients underwent anti-vascular endothelial growth factor (VEGF) intravitreal injections without improvement. Two eyes were associated with a type 3 neovascularization eccentric to PEVAC.
PEVAC is an isolated, perifoveal, aneurysmal abnormality, occurring in otherwise healthy patients who may manifest other macular disease including AMD and myopic macular degeneration. PEVAC did not typically respond to anti-VEGF therapy, and may be associated with type 3 neovascularization.
通过描述多模态成像结果,包括光学相干断层扫描血管造影(OCT-A),来扩展我们对一种罕见病症——中心凹周围渗出性血管异常复合体(PEVAC)的认识。
回顾性队列研究。
在全球4个视网膜转诊中心识别出诊断为PEVAC的患者,并对其进行全面的眼科检查,包括结构性OCT、OCT-A、荧光素血管造影(FA)和吲哚菁绿血管造影(ICGA)。在基线和可获得的随访时分析人口统计学和临床结果。
纳入15只眼(15例患者,平均年龄73±13岁)。15只眼中有6只被诊断为合并年龄相关性黄斑变性(AMD),2只合并近视性黄斑变性。眼底检查时,PEVAC表现为一个大的中心凹周围孤立性动脉瘤,15只眼中12只为单灶性,伴有小的视网膜出血和视网膜内渗出。在结构性OCT上,PEVAC表现为一个圆形高反射性病变,管腔低反射,通常被视网膜内囊样间隙包围。染料血管造影显示FA上有边界清晰的高荧光病变,有不同程度的渗漏,ICGA上无渗漏。OCT-A显示血流信号与连接视网膜毛细血管丛的动脉瘤样病变相关。7例患者随访13.0±10.5个月,无功能/解剖学改变的证据。3例患者接受玻璃体内抗血管内皮生长因子(VEGF)注射,无改善。2只眼与PEVAC偏心的3型新生血管形成相关。
PEVAC是一种孤立的、中心凹周围的、动脉瘤样异常,发生于其他方面健康的患者,这些患者可能表现出包括AMD和近视性黄斑变性在内的其他黄斑疾病。PEVAC通常对抗VEGF治疗无反应,且可能与3型新生血管形成相关。