Institut Hédi Rais d'Ophtalmologie de Tunis, Department B, Tunis, Tunisia.
Oculogenetic Laboratory LR14SP01, Tunis, Tunisia.
Eur J Ophthalmol. 2022 May;32(3):NP1-NP4. doi: 10.1177/1120672120984396. Epub 2020 Dec 24.
To report an uncommon case of aneurysmal type 1 neovascularization (polypoidal choroidal vasculopathy) secondary to high-myopic staphyloma in a Caucasian patient, assessed with multimodal imaging including swept source OCT-Angiography.
Observational case report.
About 73-year-old Caucasian male patient with high myopia (axial length = 27.24 mm). Fundus examination showed a myopic conus and a deep orange-brownish nodular lesion at the edge of a deep haemorrhage and connected to a large choroidal vessel. ICGA showed a circular hyperfluorescent lesion in mid-phase, without any branching vascular network. OCT-Angiography could detect the aneurysmal lesion non-invasively as a small circular high-flow lesion in the outer retina slab, with a shadowing in the choriocapillaris slab. At the level of the aneurysmal lesion, structural OCT showed a high bilobed PED, without any subretinal fluid. A vascular flow was noted within the PED on cross-sectional OCT-A, confirming the vascular aneurysmal nature of this lesion. Additionally, swept source OCT highlighted the presence of an abrupt change in choroidal thickness, from 62 µm in the peripapillary area to 120 µm underneath the polypoidal lesion, with dilated choroidal vessels.
To our knowledge, this is the first report of OCT-A findings in aneurysmal (polypoidal) dilation secondary to high-myopic staphyloma. We could demonstrate the usefulness of OCT-A detecting non-invasively the aneurysmal dilation and the usefulness of swept source OCT assessing the choroidal structure to better understand the pathophysiology of this uncommon finding.
报告一例罕见的高度近视性葡萄肿继发的 1 型动脉瘤样新生血管(息肉状脉络膜血管病变)病例,该病例通过包括扫频源 OCTA 在内的多种模态成像进行评估。
观察性病例报告。
患者为 73 岁白人男性,高度近视(眼轴长 27.24mm)。眼底检查显示近视性圆锥和深橙色棕色小结节状病变位于深部出血边缘,与大脉络膜血管相连。ICGA 显示中时相呈圆形高荧光病变,无任何分支血管网。OCT-A 可无创性检测到动脉瘤样病变,在外网膜层显示为小圆形高流量病变,在脉络膜毛细血管层显示阴影。在动脉瘤病变水平,结构 OCT 显示高双叶 PED,无任何视网膜下积液。在横断面 OCT-A 上观察到 PED 内有血管血流,证实了该病变的血管性动脉瘤性质。此外,扫频源 OCT 突出显示脉络膜厚度在病变下方有明显变化,从视盘周围区域的 62µm 增加到 120µm,伴有扩张的脉络膜血管。
据我们所知,这是首例报道 OCT-A 发现高度近视性葡萄肿继发的动脉瘤样(息肉状)扩张。我们能够证明 OCT-A 无创检测动脉瘤样扩张的有用性,以及扫频源 OCT 评估脉络膜结构以更好地理解这一罕见发现的病理生理学的有用性。