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Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments

PURPOSE: To report a rare case of idiopathic bilateral serous retinal pigment epithelial detachments. OBSERVATIONS: We present a case of a 43-year-old female patient with metamorphopsia with the presence of innumerable bilateral serous retinal pigment epithelial detachments. Detailed ocular and syst...

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Detalles Bibliográficos
Autores principales: Rauchegger, Teresa, Osl, Antonia, Teuchner, Barbara, Haas, Gertrud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819277/
https://www.ncbi.nlm.nih.gov/pubmed/35146203
http://dx.doi.org/10.1016/j.ajoc.2022.101336
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author Rauchegger, Teresa
Osl, Antonia
Teuchner, Barbara
Haas, Gertrud
author_facet Rauchegger, Teresa
Osl, Antonia
Teuchner, Barbara
Haas, Gertrud
author_sort Rauchegger, Teresa
collection PubMed
description PURPOSE: To report a rare case of idiopathic bilateral serous retinal pigment epithelial detachments. OBSERVATIONS: We present a case of a 43-year-old female patient with metamorphopsia with the presence of innumerable bilateral serous retinal pigment epithelial detachments. Detailed ocular and systemic clinical work-up revealed no underlying disease. CONCLUSIONS: /Importance: Idiopathic multiple serous retinal pigment epithelial detachments are an extremely rare condition, that has been observed as an incidental clinical finding in asymptomatic patients. Multimodal imaging and detailed systemic work up are essential to rule out an underlying disease. Initial symptoms, as in our case, are uncommon and usually occur only in patients with complications such as choroidal neovascularization or hemorrhages. Therefore, regular follow ups are recommended to early detect and treat possible complications.
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spelling pubmed-88192772022-02-09 Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments Rauchegger, Teresa Osl, Antonia Teuchner, Barbara Haas, Gertrud Am J Ophthalmol Case Rep Case Report PURPOSE: To report a rare case of idiopathic bilateral serous retinal pigment epithelial detachments. OBSERVATIONS: We present a case of a 43-year-old female patient with metamorphopsia with the presence of innumerable bilateral serous retinal pigment epithelial detachments. Detailed ocular and systemic clinical work-up revealed no underlying disease. CONCLUSIONS: /Importance: Idiopathic multiple serous retinal pigment epithelial detachments are an extremely rare condition, that has been observed as an incidental clinical finding in asymptomatic patients. Multimodal imaging and detailed systemic work up are essential to rule out an underlying disease. Initial symptoms, as in our case, are uncommon and usually occur only in patients with complications such as choroidal neovascularization or hemorrhages. Therefore, regular follow ups are recommended to early detect and treat possible complications. Elsevier 2022-01-22 /pmc/articles/PMC8819277/ /pubmed/35146203 http://dx.doi.org/10.1016/j.ajoc.2022.101336 Text en © 2022 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Rauchegger, Teresa
Osl, Antonia
Teuchner, Barbara
Haas, Gertrud
Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments
title Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments
title_full Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments
title_fullStr Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments
title_full_unstemmed Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments
title_short Symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments
title_sort symptomatic idiopathic bilateral multifocal retinal pigment epithelial detachments
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819277/
https://www.ncbi.nlm.nih.gov/pubmed/35146203
http://dx.doi.org/10.1016/j.ajoc.2022.101336
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