Medina-Baena Marta, Huertos-Carrillo María Jesús, Rodríguez Laura, García-Pulido Juan Ignacio, Cornejo-Castillo Carlos, Calandria-Amiguetti José María
Unidad de Retina y Vítreo, Hospital Universitario Puerto Real, Cádiz, Spain.
Unidad de Retina y Vítreo, Hospital Universitario Puerta del Mar, Cádiz, Spain.
Case Rep Ophthalmol. 2018 Mar 2;9(1):172-178. doi: 10.1159/000487227. eCollection 2018 Jan-Apr.
Polypoidal choroidal vasculopathy (PCV) is a subtype of neovascular age-related macular degeneration characterised by an abnormal branching vascular network with aneurysmal polypoidal choroidal vascular lesions. PCV is more prevalent in Asian populations than in Caucasians, which may explain its underdiagnosis in Western countries. Evidence regarding the efficacy of different anti-vascular endothelial growth factor (anti-VEGF) agents on PCV is scarce, with most of these studies being conducted in Asian treatment-naïve patients. Ranibizumab was the first anti-VEGF agent to demonstrate the superiority of a combination of photodynamic therapy (PDT) and anti-VEGF over PDT or anti-VEGF monotherapy for inducing polyp regression in Asian patients with PCV. The efficacy of other anti-VEGF agents has been less studied. Resistance to ranibizumab has been described. Aflibercept offers another mechanism of targeting choroidal neovascular lesions. A 75-year-old Caucasian woman presenting to our office was diagnosed with PCV using indocyanine green angiography. Combination therapy with a loading dose of 0.5 mg intravitreal ranibizumab followed by PDT at standard fluence at month 4 and a fourth dose of ranibizumab at month 5 yielded no visual or anatomic outcomes. Treatment was switched to intravitreal aflibercept at month 6 (3 monthly loading doses of 2.0 mg) followed by half-fluence PDT (month 9). Optical coherence tomography revealed remission of the anatomic lesions. Right-eye visual acuity increased to 0.6. Aflibercept injections were administered bimonthly afterwards. Follow-up during 1 year has shown functional and anatomic stability.
息肉样脉络膜血管病变(PCV)是新生血管性年龄相关性黄斑变性的一种亚型,其特征是具有动脉瘤样息肉样脉络膜血管病变的异常分支血管网络。PCV在亚洲人群中比在白种人中更普遍,这可能解释了其在西方国家诊断不足的原因。关于不同抗血管内皮生长因子(抗VEGF)药物对PCV疗效的证据很少,这些研究大多在亚洲初治患者中进行。雷珠单抗是第一种证明光动力疗法(PDT)联合抗VEGF在诱导亚洲PCV患者息肉消退方面优于PDT或抗VEGF单药治疗的抗VEGF药物。其他抗VEGF药物的疗效研究较少。已有对雷珠单抗耐药的报道。阿柏西普提供了另一种靶向脉络膜新生血管病变的机制。一名75岁的白种女性到我们诊所就诊,通过吲哚菁绿血管造影被诊断为PCV。采用玻璃体内注射0.5mg雷珠单抗负荷剂量,随后在第4个月以标准能量密度进行PDT,并在第5个月注射第四剂雷珠单抗的联合治疗未产生视觉或解剖学效果。在第6个月将治疗改为玻璃体内注射阿柏西普(每月3次负荷剂量2.0mg),随后在第9个月进行半能量密度PDT。光学相干断层扫描显示解剖学病变缓解。右眼视力提高到0.6。此后每两个月注射一次阿柏西普。1年的随访显示功能和解剖学稳定。