Forte Raimondo, Aptel Florent, Feldmann Audrey, Chiquet Christophe
Department of Ophthalmology, Grenoble Alpes University, University Hospital of Grenoble, Grenoble, France.
Retin Cases Brief Rep. 2018;12(1):29-32. doi: 10.1097/ICB.0000000000000400.
Posterior polar annular choroidal dystrophy (PPACD) is a rare disease. Patients with PPACD show loss of retinal pigment epithelium and choriocapillaries surrounding the vascular arcades and optic nerve.
Two patients with PPACD were evaluated with multimodal imaging, including fundus autofluorescence (FAF) and adaptive optics (AO).
One patient (32 year old, one eye) with PPACD was followed up for 3 years. Best-corrected visual acuity (BCVA) was stable at 20/40, whereas a slight enlargement of paravascular atrophy of pigment epithelium was observed at fundus autofluorescence (FAF). Adaptive optics obtained at last examination showed reduced density of foveal cone photoreceptors. The second patient (30 year old, two eyes) with PPACD showed bilateral normal BCVA, associated with reduction in the density of foveal cone photoreceptors.
At FAF, longitudinal follow-up of PPACD showed progression of the paravascular atrophy of the pigment epithelium. Foveal cone photoreceptors can be reduced even in the presence of preserved visual acuity.
后极部环状脉络膜营养不良(PPACD)是一种罕见疾病。PPACD患者表现为视网膜色素上皮以及围绕血管弓和视神经的脉络膜毛细血管缺失。
对两名PPACD患者进行了多模态成像评估,包括眼底自发荧光(FAF)和自适应光学(AO)。
一名PPACD患者(32岁,单眼)随访3年。最佳矫正视力(BCVA)稳定在20/40,而眼底自发荧光(FAF)显示色素上皮血管旁萎缩略有扩大。最后一次检查时的自适应光学检查显示中央凹视锥光感受器密度降低。第二名PPACD患者(30岁,双眼)BCVA双侧正常,伴有中央凹视锥光感受器密度降低。
在眼底自发荧光(FAF)检查中,PPACD的纵向随访显示色素上皮血管旁萎缩进展。即使视力保持正常,中央凹视锥光感受器也可能减少。