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Full-Thickness Macular Hole with Coats Disease: A Case Report

We report a case of full-thickness macular hole (FTMH) which developed during follow-up for Coats disease. To our knowledge, this is the first report on a case of FTMH which developed during follow-up for Coats disease. A 17-year-old boy was referred to our institution with blurred vision in his lef...

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Autores principales: Hashimoto, Yuto, Arai, Yusuke, Makino, Shinji, Inoue, Yuji, Takahashi, Hidenori, Kawashima, Hidetoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443633/
https://www.ncbi.nlm.nih.gov/pubmed/32884548
http://dx.doi.org/10.1159/000508821
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author Hashimoto, Yuto
Arai, Yusuke
Makino, Shinji
Inoue, Yuji
Takahashi, Hidenori
Kawashima, Hidetoshi
author_facet Hashimoto, Yuto
Arai, Yusuke
Makino, Shinji
Inoue, Yuji
Takahashi, Hidenori
Kawashima, Hidetoshi
author_sort Hashimoto, Yuto
collection PubMed
description We report a case of full-thickness macular hole (FTMH) which developed during follow-up for Coats disease. To our knowledge, this is the first report on a case of FTMH which developed during follow-up for Coats disease. A 17-year-old boy was referred to our institution with blurred vision in his left eye. Fundus examination showed yellowish subretinal exudates with overlying telangiectatic retinal vessels in the temporal periphery in the left eye; the right eye was normal. Fluorescein angiography revealed diffusion indicative of temporal peripheral vascular leakage. We made a diagnosis of stage 2A Coats disease and performed argon laser photocoagulation (PC). Moreover, he received intravitreal injection of anti-vascular endothelial growth factor. At 30 months after the first visit, the best-corrected visual acuity (BCVA) of the left eye worsened to 20/50. We observed tensioned internal limiting membrane (ILM), serous macular detachment (SMD) and retinal thinning; the intraretinal exudate remained. We performed PC and at 36 months after the first visit, BCVA further declined to 20/63 in his left eye and FTMH was observed. We then performed a 27-gauge pars plana vitrectomy and ILM peeling following which the FTMH was found to have closed by 4 days after vitrectomy. SMD gradually decreased, and BCVA improved to 20/20. Chronic inflammation by peripheral vascular leakage and PC application might have caused FTMH. In this case, the vitrectomy for FTMH with Coats disease provided good visual and anatomic outcomes.
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spelling pubmed-74436332020-09-02 Full-Thickness Macular Hole with Coats Disease: A Case Report Hashimoto, Yuto Arai, Yusuke Makino, Shinji Inoue, Yuji Takahashi, Hidenori Kawashima, Hidetoshi Case Rep Ophthalmol Case Report We report a case of full-thickness macular hole (FTMH) which developed during follow-up for Coats disease. To our knowledge, this is the first report on a case of FTMH which developed during follow-up for Coats disease. A 17-year-old boy was referred to our institution with blurred vision in his left eye. Fundus examination showed yellowish subretinal exudates with overlying telangiectatic retinal vessels in the temporal periphery in the left eye; the right eye was normal. Fluorescein angiography revealed diffusion indicative of temporal peripheral vascular leakage. We made a diagnosis of stage 2A Coats disease and performed argon laser photocoagulation (PC). Moreover, he received intravitreal injection of anti-vascular endothelial growth factor. At 30 months after the first visit, the best-corrected visual acuity (BCVA) of the left eye worsened to 20/50. We observed tensioned internal limiting membrane (ILM), serous macular detachment (SMD) and retinal thinning; the intraretinal exudate remained. We performed PC and at 36 months after the first visit, BCVA further declined to 20/63 in his left eye and FTMH was observed. We then performed a 27-gauge pars plana vitrectomy and ILM peeling following which the FTMH was found to have closed by 4 days after vitrectomy. SMD gradually decreased, and BCVA improved to 20/20. Chronic inflammation by peripheral vascular leakage and PC application might have caused FTMH. In this case, the vitrectomy for FTMH with Coats disease provided good visual and anatomic outcomes. S. Karger AG 2020-07-14 /pmc/articles/PMC7443633/ /pubmed/32884548 http://dx.doi.org/10.1159/000508821 Text en Copyright © 2020 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Hashimoto, Yuto
Arai, Yusuke
Makino, Shinji
Inoue, Yuji
Takahashi, Hidenori
Kawashima, Hidetoshi
Full-Thickness Macular Hole with Coats Disease: A Case Report
title Full-Thickness Macular Hole with Coats Disease: A Case Report
title_full Full-Thickness Macular Hole with Coats Disease: A Case Report
title_fullStr Full-Thickness Macular Hole with Coats Disease: A Case Report
title_full_unstemmed Full-Thickness Macular Hole with Coats Disease: A Case Report
title_short Full-Thickness Macular Hole with Coats Disease: A Case Report
title_sort full-thickness macular hole with coats disease: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443633/
https://www.ncbi.nlm.nih.gov/pubmed/32884548
http://dx.doi.org/10.1159/000508821
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