4.4 Article

Multimodal imaging comparison of perifoveal exudative vascular anomalous complex and resembling lesions

期刊

ACTA OPHTHALMOLOGICA
卷 99, 期 5, 页码 553-558

出版社

WILEY
DOI: 10.1111/aos.14650

关键词

aneurysm; clinical; imaging; morphological; perifoveal exudative vascular anomalous complex; PEVAC‐ resembling; retinal; vascular

资金

  1. Rotterdamse Stichting Blindenbelangen (RSB), Rotterdam, the Netherlands [B20180055]
  2. Stichting Wetenschappelijk Onderzoek Oogziekenhuis (SWOO), Rotterdam, the Netherlands [2018S04]

向作者/读者索取更多资源

Based on multimodal imaging, the clinical, morphological, and vascular features of PEVAC and PEVAC-resembling lesions are similar. The bilaterality and multifocality seen in PEVAC-resembling lesions may be stimulated by underlying retinal vascular diseases, increasing the quantity of aneurysmal abnormalities. Due to similarities with PEVAC-resembling lesions, PEVAC may also be considered a microangiopathy with unknown origin.
Purpose Perifoveal exudative vascular anomalous complex (PEVAC) was initially described as an isolated aneurysmal lesion in healthy eyes. Similar aneurysmal abnormalities may occur in association with retinal vascular diseases such as diabetic retinopathy or retinal vein occlusions (PEVAC-resembling). The aim of this study was to compare several imaging characteristics of PEVAC and PEVAC-resembling lesions. Methods Ten eyes with a PEVAC and 27 eyes with a PEVAC-resembling lesion were included in this cross-sectional study. They were all imaged with optical coherence tomography (OCT), OCT angiography (OCT-A) and colour fundus photography (CFP). Several clinical, morphological and vascular characteristics were assessed and compared between both PEVAC types. Results All PEVAC lesions were unilateral, while PEVAC-resembling lesions appeared bilateral in 23% of patients (p > 0.05). Unilateral multifocal PEVAC-resembling lesions were more frequently observed (56%) than unilateral multifocal PEVAC lesions (10%, p < 0.01). Furthermore, 90% of the PEVAC lesions were located within 500 mu m from the centre of the fovea, while this was only true for 56% of the PEVAC-resembling lesions (p > 0.05). No notable differences were observed in other studied characteristics. Conclusions The clinical, morphological and vascular features of PEVAC and PEVAC-resembling lesions are similar based on multimodal imaging. Given the bilaterality and multifocality seen in PEVAC-resembling lesions, an underlying retinal vascular disease may stimulate the quantity of aneurysmal abnormalities. Due to the similarities with PEVAC-resembling lesions, PEVAC may also be considered a microangiopathy but with an unknown origin.

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