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Topographic patterns of retinal lesions in multiple evanescent white dot syndrome
PURPOSE: To demonstrate different topographic distributions of multiple-evanescent white dot syndrome (MEWDS) and secondary MEWDS disease and to describe possible associations. METHODS: Clinical evaluation and multimodal retinal imaging in 27 subjects with MEWDS (29 discrete episodes of MEWDS). Opht...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368570/ https://www.ncbi.nlm.nih.gov/pubmed/36988677 http://dx.doi.org/10.1007/s00417-023-06032-1 |
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author | Ong, Ariel Yuhan Birtel, Johannes Agorogiannis, Eleftherios Sharma, Srilakshmi M. Charbel Issa, Peter |
author_facet | Ong, Ariel Yuhan Birtel, Johannes Agorogiannis, Eleftherios Sharma, Srilakshmi M. Charbel Issa, Peter |
author_sort | Ong, Ariel Yuhan |
collection | PubMed |
description | PURPOSE: To demonstrate different topographic distributions of multiple-evanescent white dot syndrome (MEWDS) and secondary MEWDS disease and to describe possible associations. METHODS: Clinical evaluation and multimodal retinal imaging in 27 subjects with MEWDS (29 discrete episodes of MEWDS). Ophthalmic assessment included best-corrected visual acuity testing and multimodal retinal imaging with OCT, blue-light autofluorescence, fluorescein and indocyanine green angiography, fundus photography, and widefield pseudocolor and autofluorescence fundus imaging. RESULTS: The topographic distribution of MEWDS lesions was centered on or around the optic disc (n = 17, 59%), centered on the macula (n = 7, 24%), sectoral (n = 2, 7%), or was indeterminate (n = 3, 10%). The MEWDS episodes either occurred in the absence (‘primary MEWDS’; n = 14, 48%) or presence of concurrent chorioretinal pathology (‘secondary MEWDS’; n = 15, 52%). In patients with the latter, MEWDS lesions were often centered around a coexisting chorioretinal lesion. The majority of patients in both groups experienced resolution of their symptoms and retinal changes on multimodal imaging by 3 months. CONCLUSIONS: Distinct distributions of MEWDS lesions were identified. MEWDS may occur in tandem with other chorioretinal pathology, which may impact the topography of MEWDS lesions. [Image: see text] |
format | Online Article Text |
id | pubmed-10368570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103685702023-07-27 Topographic patterns of retinal lesions in multiple evanescent white dot syndrome Ong, Ariel Yuhan Birtel, Johannes Agorogiannis, Eleftherios Sharma, Srilakshmi M. Charbel Issa, Peter Graefes Arch Clin Exp Ophthalmol Retinal Disorders PURPOSE: To demonstrate different topographic distributions of multiple-evanescent white dot syndrome (MEWDS) and secondary MEWDS disease and to describe possible associations. METHODS: Clinical evaluation and multimodal retinal imaging in 27 subjects with MEWDS (29 discrete episodes of MEWDS). Ophthalmic assessment included best-corrected visual acuity testing and multimodal retinal imaging with OCT, blue-light autofluorescence, fluorescein and indocyanine green angiography, fundus photography, and widefield pseudocolor and autofluorescence fundus imaging. RESULTS: The topographic distribution of MEWDS lesions was centered on or around the optic disc (n = 17, 59%), centered on the macula (n = 7, 24%), sectoral (n = 2, 7%), or was indeterminate (n = 3, 10%). The MEWDS episodes either occurred in the absence (‘primary MEWDS’; n = 14, 48%) or presence of concurrent chorioretinal pathology (‘secondary MEWDS’; n = 15, 52%). In patients with the latter, MEWDS lesions were often centered around a coexisting chorioretinal lesion. The majority of patients in both groups experienced resolution of their symptoms and retinal changes on multimodal imaging by 3 months. CONCLUSIONS: Distinct distributions of MEWDS lesions were identified. MEWDS may occur in tandem with other chorioretinal pathology, which may impact the topography of MEWDS lesions. [Image: see text] Springer Berlin Heidelberg 2023-03-29 2023 /pmc/articles/PMC10368570/ /pubmed/36988677 http://dx.doi.org/10.1007/s00417-023-06032-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Retinal Disorders Ong, Ariel Yuhan Birtel, Johannes Agorogiannis, Eleftherios Sharma, Srilakshmi M. Charbel Issa, Peter Topographic patterns of retinal lesions in multiple evanescent white dot syndrome |
title | Topographic patterns of retinal lesions in multiple evanescent white dot syndrome |
title_full | Topographic patterns of retinal lesions in multiple evanescent white dot syndrome |
title_fullStr | Topographic patterns of retinal lesions in multiple evanescent white dot syndrome |
title_full_unstemmed | Topographic patterns of retinal lesions in multiple evanescent white dot syndrome |
title_short | Topographic patterns of retinal lesions in multiple evanescent white dot syndrome |
title_sort | topographic patterns of retinal lesions in multiple evanescent white dot syndrome |
topic | Retinal Disorders |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368570/ https://www.ncbi.nlm.nih.gov/pubmed/36988677 http://dx.doi.org/10.1007/s00417-023-06032-1 |
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