Vieira Rita, Furtado Maria João
Ophthalmology Department of Centro Hospitalar Universitário do Porto (CHUPorto), Oporto, Portugal.
Int Med Case Rep J. 2022 Sep 30;15:543-549. doi: 10.2147/IMCRJ.S369324. eCollection 2022.
To describe a case of long-term poorly treated bilateral acute syphilitic posterior placoid chorioretinitis (ASPPC) complicated with choroidal neovascularization, with a multimodal imaging approach.
Retrospective case report. Analysis of patient's clinical data.
A healthy 66-year-old man complained of decreased visual acuity in the right eye (RE). He had a past history of bilateral exudative maculopathy of unknown etiology, lasting for more than 10 years and leading to severe and irreversible vision loss on the left eye. The corrected distance visual acuity (CDVA) was 20/63 on the RE and <20/400 on the left eye (LE). On slit-lamp, no anterior chamber reaction was observed, a vitreous haze was present on the RE as well as large, bilateral yellowish lesions in the macula, with exuberant macular atrophy, particularly on the LE. These well-defined lesions were confined to the posterior pole. The spectral domain optical coherence tomography (SD-OCT) showed a flat retinal pigmented epithelium (RPE) detachment with hyperreflective material beneath the RPE and cystoid macular edema on the RE and an exuberant macular atrophy on the LE, with both eyes showing anomalous enlargement of choroidal vessels. The fluorescein angiography showed general hypofluorescence and indocyanine green angiography revealed a heterogeneous pattern. The OCT angiography (OCTA) of the RE demonstrated an anomalous vascular network related to the presence of choroidal neovascularization (CNV). An etiological study was performed and a positive treponemal test (TPHA) was found. The patient experienced visual acuity improvement to 20/25 after systemic treatment with Penicillin and anti-VEGF injections.
Clinical data and multimodal imaging information suggest that this case represents a complication of long-term untreated bilateral acute syphilitic posterior placoid chorioretinitis (ASPPC) with associated choroidal neovascularization. Once the RE presented signs of active disease, besides intravitreal anti-VEGF, treatment of the underlying disease was essential for visual recovery.
通过多模态成像方法描述一例长期治疗不佳的双侧急性梅毒性后极部扁平状脉络膜视网膜病变(ASPPC)合并脉络膜新生血管的病例。
回顾性病例报告。分析患者的临床资料。
一名66岁健康男性主诉右眼视力下降。他有双侧病因不明的渗出性黄斑病变病史,持续超过10年,导致左眼严重且不可逆的视力丧失。右眼矫正远视力(CDVA)为20/63,左眼<20/400。裂隙灯检查显示无前房反应,右眼有玻璃体混浊,黄斑区有双侧大的淡黄色病变,黄斑萎缩明显,尤其是左眼。这些边界清晰的病变局限于后极部。频域光学相干断层扫描(SD-OCT)显示右眼视网膜色素上皮(RPE)扁平脱离,RPE下方有高反射物质及黄斑囊样水肿,左眼黄斑萎缩明显,双眼均显示脉络膜血管异常增粗。荧光素血管造影显示普遍低荧光,吲哚菁绿血管造影显示不均匀模式。右眼的光学相干断层扫描血管造影(OCTA)显示与脉络膜新生血管(CNV)相关的异常血管网络。进行了病因学研究,发现梅毒螺旋体试验阳性(TPHA)。患者经青霉素全身治疗及抗VEGF注射后视力提高至20/25。
临床资料和多模态成像信息表明,该病例代表长期未治疗的双侧急性梅毒性后极部扁平状脉络膜视网膜病变(ASPPC)合并脉络膜新生血管的并发症。一旦右眼出现活动性疾病迹象,除眼内注射抗VEGF外,治疗潜在疾病对视力恢复至关重要。