Tsui Edmund, Gal-Or Orly, Ghadiali Quraish, Freund K Bailey
Department of Ophthalmology, New York University School of Medicine, New York, New York.
Vitreous Retina Macula Consultants of New York, New York, New York.
Retin Cases Brief Rep. 2018;12 Suppl 1:S3-S8. doi: 10.1097/ICB.0000000000000645.
Acute syphilitic posterior placoid chorioretinitis (ASPPC) is an uncommon manifestation of ocular syphilis with distinct clinical features. We describe new multimodal imaging findings in a patient with ASPPC.
Observational case report with multimodal imaging.
A 44-year-old woman presented with 5 days of decreased vision in her right eye. Visual acuity was counting fingers in her right eye and 20/20 in her left eye. Funduscopic examination of the right eye showed a yellow placoid macular lesion with extension beyond the equator, which was encircled by an annular ring of outer retinal whitening. Ultra-widefield fundus autofluorescence demonstrated hyperautofluorescence corresponding to the placoid lesion. Examination of the left eye appeared unremarkable, but ultra-widefield fundus autofluorescence showed an area of hyperautofluorescence located superonasal to the optic nerve. Optical coherence tomography of the right eye demonstrated subretinal fluid and overlying disruption of the ellipsoid zone. Fluorescein angiography demonstrated early hypofluorescent and hyperfluorescent spots and late staining within the placoid lesion. Optical coherence tomography angiography showed several areas of decreased flow signal within the placoid lesion at the level of the choriocapillaris. Laboratory testing revealed a rapid plasma reagin titer of 1:1,024. Two months after treatment with intravenous penicillin G, visual acuity had improved to 20/25 in her right eye, and optical coherence tomography showed partial restoration of the ellipsoid zone. The annular ring resolved with near normalization of fundus autofluorescence and optical coherence tomography angiography demonstrated resolution of flow.
Multimodal imaging provides further insight into the pathogenesis of ASPPC. Ultra-widefield fundus autofluorescence may show evidence of ellipsoid zone disruption in areas that clinically appear normal. Flow voids within the choriocapillaris in ASPPC appear to resolve with appropriate treatment, a finding that suggests a transient disruption of choriocapillaris flow in ASPPC.
急性梅毒性后极部扁平状脉络膜视网膜病变(ASPPC)是眼梅毒的一种罕见表现,具有独特的临床特征。我们描述了1例ASPPC患者的新的多模态影像学表现。
采用多模态影像学的观察性病例报告。
一名44岁女性,右眼视力下降5天。右眼视力为眼前指数,左眼视力为20/20。右眼眼底检查显示黄斑区有一黄色扁平状病变,延伸至赤道以外,病变周围有外层视网膜变白形成的环形圈。超广角眼底自发荧光显示与扁平状病变对应的高自发荧光。左眼检查未见明显异常,但超广角眼底自发荧光显示视神经鼻上方有一高自发荧光区。右眼光学相干断层扫描显示视网膜下液及上方椭圆体带中断。荧光素血管造影显示扁平状病变内早期低荧光和高荧光斑点及晚期染色。光学相干断层扫描血管造影显示扁平状病变内脉络膜毛细血管层有几个血流信号减弱区。实验室检查显示快速血浆反应素滴度为1:1024。静脉注射青霉素G治疗2个月后,右眼视力提高到20/25,光学相干断层扫描显示椭圆体带部分恢复。环形圈消失,眼底自发荧光接近正常,光学相干断层扫描血管造影显示血流消失。
多模态影像学有助于进一步了解ASPPC的发病机制。超广角眼底自发荧光可能显示临床外观正常区域的椭圆体带中断迹象。ASPPC患者脉络膜毛细血管层的血流缺失在适当治疗后似乎会消失,这一发现提示ASPPC患者脉络膜毛细血管层血流存在短暂中断。