OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY OF CHOROIDAL NEOVASCULARIZATION IN FOUR INHERITED RETINAL DYSTROPHIES.
OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY OF CHOROIDAL NEOVASCULARIZATION IN FOUR INHERITED RETINAL DYSTROPHIES.
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DOI:
10.1097/iae.0000000000001159
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发表时间:
2016-12
期刊:
影响因子:
--
通讯作者:
Pennesi ME
中科院分区:
文献类型:
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作者:
Patel RC;Gao SS;Zhang M;Alabduljalil T;Al-Qahtani A;Weleber RG;Yang P;Jia Y;Huang D;Pennesi ME
To demonstrate the clinical utility of optical coherence tomography (OCT) angiography (OCT-A) in inherited retinal dystrophies (IRDs) complicated by choroidal neovascularization (CNV). OCT-A and structural OCT were performed using a 70 kHz spectral-domain OCT system employing the split-spectrum amplitude-decorrelation angiography algorithm. Semiautomated image processing software was used to segment and measure the CNV. Four participants were enrolled to study the following IRDs complicated by CNV: choroideremia, EFEMP1-related retinopathy, Best vitelliform dystrophy, and adult-onset vitelliform dystrophy. Interpretation of fluorescein angiography was difficult due to abnormal retinal architecture but suggested the presence of CNV. Structural OCT revealed subretinal or sub-RPE fibrovascular tissue, within which flow signal was observed on OCT-A. CNV morphology varied from dense capillary networks in active lesions to asymptomatic large caliber loops. Baseline CNV vessel areas ranged from 0.07 to 0.98 mm2. Following treatment with intravitreal bevacizumab, the CNV in choroideremia decreased in vessel area then rebounded, while the one in EFEMP1-related retinopathy remained largely unchanged. OCT-A enables the morphologic characterization and quantification of CNV in patients with retinal dystrophies despite distorted retinal architecture, can assess response to treatment, and may facilitate the differentiation between active and regressed lesions.