Primary and secondary focal choroidal excavation morphologic phenotypes, associated ocular disorders and prognostic implications

医学 浆液性液体 脉络膜新生血管 眼底(子宫) 眼科 脉络膜 病理 视网膜 视网膜 光学 物理
作者
Pamela Capellàn,Luis Alonso González,Mervat Mahrous,Soma Weiss,Benjamin Botsford,Tamara L. Lenis,Michaël Ryan,Anton Orlin,Thanos D. Papakostas,Szilárd Kiss,Donald J. D’Amico,Kyle D. Kovacs
出处
期刊:British Journal of Ophthalmology [BMJ]
卷期号:107 (3): 373-379 被引量:4
标识
DOI:10.1136/bjophthalmol-2021-319569
摘要

To characterise and classify the morphological, clinical and tomographic characteristics of focal choroidal excavation (FCE) lesions to determine their prognostic implications.36 eyes with FCE (32 patients) underwent multimodal imaging, including spectral domain optical coherence tomography and fundus autofluorescence. FCE lesions were classified into three subtypes: (1) type 1: myopic (central choroidal thickness: <100 µm), (2) type 2: suspected congenital (central choroidal thickness: 100-200 µm, without associated chorioretinal pathology) and (3) type 3: secondary or acquired (central choroidal thickness: >200 µm, with associated chorioretinal pathology).80.6% of eyes were followed longitudinally (26.8±18.8 months). There were 9 type 1 FCEs (myopic), 8 type 2 FCEs (U-shaped, congenital) and 19 type 3 FCEs (V-shaped, secondary). Type 2 FCEs trended towards larger maximum widths (p=0.0563). Type 3 FCEs were associated with central serous chorioretinopathy or pachyvessels (47.4%), but were also seen in pattern dystrophy, geographic atrophy, inactive choroiditis, torpedo maculopathy and adult-onset vitelliform dystrophy. Choroidal neovascular membranes (CNVMs) were more prevalent in type 3 FCE (41.2% compared with 11.1% for type 1 FCE, p=0.251, and 0% for type 2 FCE, p=0.043).The FCE types, stratified by central choroidal thickness, demonstrated distinct morphological characteristics and associated findings. The classification scheme held prognostic implications as type 3 FCE with V shapes were associated with other chorioretinal conditions and were more likely to develop CNVM.
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