Department of Ophthalmology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, N-15, W-7, Kita-Ku, Sapporo, 060-8638, Japan.
Department of Ophthalmology, Health Sciences University of Hokkaido, Sapporo, Japan.
BMC Ophthalmol. 2023 May 24;23(1):233. doi: 10.1186/s12886-023-02978-2.
Vaccination against the worldwide pandemic coronavirus disease 2019 (COVID-19) is underway; however, some cases of new onset uveitis after vaccination have been reported. We report a case of bilateral acute posterior multifocal placoid pigment epitheliopathy-like (AMPPE-like) panuveitis after COVID-19 vaccination in which the patient's pathological condition was evaluated using multimodal imaging.
A 31-year-old woman experienced bilateral hyperemia and blurred vision starting 6 days after her second inoculation of the COVID-19 vaccination. At her first visit, her visual acuity was decreased bilaterally, and severe bilateral anterior chamber inflammation and bilateral scattering of cream-white placoid lesions on the fundus were detected. Optical coherence tomography (OCT) showed serous retinal detachment (SRD) and choroidal thickening in both eyes (OU). Fluorescein angiography (FA) revealed hypofluorescence in the early phase and hyperfluorescence in the late phase corresponding to the placoid legions. Indocyanine green angiography (ICGA) showed sharply marginated hypofluorescent dots of various sizes throughout the mid-venous and late phases OU. The patient was diagnosed with APMPPE and was observed without any medications. Three days later, her SRD disappeared spontaneously. However, her anterior chamber inflammation continued, and oral prednisolone (PSL) was given to her. Seven days after the patient's first visit, the hyperfluorescent lesions on FA and hypofluorescent dots on ICGA partially improved; however, the patient's best corrected visual acuity (BCVA) recovered only to 0.7 OD and 0.6 OS, and the impairment of the outer retinal layer was broadly detected as hyperautofluorescent lesions on fundus autofluorescence (FAF) examination and as irregularity in or disappearance of the ellipsoid and interdigitation zones on OCT, which were quite atypical for the findings of APMPPE. Steroid pulse therapy was performed. Five days later, the hyperfluorescence on FAF had disappeared, and the outer retinal layer improved on OCT. Moreover, the patient's BCVA recovered to 1.0 OU. Twelve months after the end of treatment, the patient did not show any recurrences.
We observed a case of APMPPE-like panuveitis after COVID-19 vaccination featuring some atypical findings for APMPPE. COVID-19 vaccination may induce not only known uveitis but also atypical uveitis, and appropriate treatment is required for each case.
针对 2019 年冠状病毒病(COVID-19)的全球大流行,疫苗接种正在进行中;然而,有报道称接种疫苗后会出现新的葡萄膜炎病例。我们报告了一例 COVID-19 疫苗接种后双侧急性后多发性多灶性脉络膜视网膜炎样(AMPPE 样)全葡萄膜炎,对患者的病理状况进行了多模态成像评估。
一名 31 岁女性,在第二次接种 COVID-19 疫苗后 6 天出现双侧眼红和视力模糊。首次就诊时,她的双眼视力均下降,双眼严重前房炎症,眼底出现双侧奶油色斑块状病变。光学相干断层扫描(OCT)显示双眼均有浆液性视网膜脱离(SRD)和脉络膜增厚。荧光素血管造影(FA)显示早期低荧光,晚期高荧光与斑块状病变相对应。吲哚青绿血管造影(ICGA)显示整个中静脉和晚期 OU 均有大小不一的边界清晰的低荧光点。患者被诊断为 APMPPE,未给予任何药物治疗。三天后,她的 SRD 自行消失。然而,她的前房炎症持续存在,给予她口服泼尼松龙(PSL)。患者首次就诊后 7 天,FA 上的高荧光病变和 ICGA 上的低荧光点部分改善;然而,她的最佳矫正视力(BCVA)仅恢复至 0.7 OD 和 0.6 OS,眼底自发荧光(FAF)检查显示外视网膜层广泛出现高自发荧光病变,OCT 显示椭圆体和内插带不规则或消失,这与 APMPPE 的发现非常不典型。给予了类固醇脉冲治疗。五天后,FAF 上的高荧光消失,OCT 上的外视网膜层改善。此外,患者的 BCVA 恢复至 1.0 OU。治疗结束后 12 个月,患者未出现任何复发。
我们观察到一例 COVID-19 疫苗接种后出现的 AMPPE 样全葡萄膜炎,其表现出一些与 AMPPE 不典型的发现。COVID-19 疫苗接种不仅可诱发已知的葡萄膜炎,还可诱发非典型葡萄膜炎,因此需要针对每个病例进行适当的治疗。