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Fundus flavimaculatus-like in myotonic dystrophy: a case report
BACKGROUND: Myotonic dystrophy is an inherited disease characterized by progressive muscle weakness and myotonia. It is a multisystemic disorder that affects different parts of the body, including the eye. Dysfunction of ocular muscles, ptosis and cataract are the most common ophthalmologic manifest...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164789/ https://www.ncbi.nlm.nih.gov/pubmed/34051736 http://dx.doi.org/10.1186/s12886-021-02002-5 |
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author | Kirkegaard-Biosca, Eric Berges-Marti, Mònica Azarfane, Brahim Cilveti, Esther Distefano, Laura García-Arumí, Jose |
author_facet | Kirkegaard-Biosca, Eric Berges-Marti, Mònica Azarfane, Brahim Cilveti, Esther Distefano, Laura García-Arumí, Jose |
author_sort | Kirkegaard-Biosca, Eric |
collection | PubMed |
description | BACKGROUND: Myotonic dystrophy is an inherited disease characterized by progressive muscle weakness and myotonia. It is a multisystemic disorder that affects different parts of the body, including the eye. Dysfunction of ocular muscles, ptosis and cataract are the most common ophthalmologic manifestations, but it can also present with pigmentary changes in the retina. This report presents and discusses an unusual case of a pigmented pattern dystrophy simulating a fundus flavimaculatus in a patient with myotonic dystrophy. CASE PRESENTATION: We present a case of a woman with a history of myotonic dystrophy and complaints of progressive vision loss who presented bilateral retinal pigmentary changes in posterior pole and midperiphery. The characteristics and distribution of pigmented deposits, as well as ancillary tests, showed a retinal phenotype compatible with a multifocal pattern dystrophy or a fundus flavimaculatus. CONCLUSIONS: There are a few publications about retinal disorders in patients with myotonic dystrophy. When macular area is affected it tends to adopt a patterned-shape defined as butterfly dystrophy or reticular dystrophy. To our knowledge, this is the first report of a patient with myotonic dystrophy and multifocal pattern dystrophy or fundus flavimaculatus. |
format | Online Article Text |
id | pubmed-8164789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81647892021-06-01 Fundus flavimaculatus-like in myotonic dystrophy: a case report Kirkegaard-Biosca, Eric Berges-Marti, Mònica Azarfane, Brahim Cilveti, Esther Distefano, Laura García-Arumí, Jose BMC Ophthalmol Case Report BACKGROUND: Myotonic dystrophy is an inherited disease characterized by progressive muscle weakness and myotonia. It is a multisystemic disorder that affects different parts of the body, including the eye. Dysfunction of ocular muscles, ptosis and cataract are the most common ophthalmologic manifestations, but it can also present with pigmentary changes in the retina. This report presents and discusses an unusual case of a pigmented pattern dystrophy simulating a fundus flavimaculatus in a patient with myotonic dystrophy. CASE PRESENTATION: We present a case of a woman with a history of myotonic dystrophy and complaints of progressive vision loss who presented bilateral retinal pigmentary changes in posterior pole and midperiphery. The characteristics and distribution of pigmented deposits, as well as ancillary tests, showed a retinal phenotype compatible with a multifocal pattern dystrophy or a fundus flavimaculatus. CONCLUSIONS: There are a few publications about retinal disorders in patients with myotonic dystrophy. When macular area is affected it tends to adopt a patterned-shape defined as butterfly dystrophy or reticular dystrophy. To our knowledge, this is the first report of a patient with myotonic dystrophy and multifocal pattern dystrophy or fundus flavimaculatus. BioMed Central 2021-05-29 /pmc/articles/PMC8164789/ /pubmed/34051736 http://dx.doi.org/10.1186/s12886-021-02002-5 Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Kirkegaard-Biosca, Eric Berges-Marti, Mònica Azarfane, Brahim Cilveti, Esther Distefano, Laura García-Arumí, Jose Fundus flavimaculatus-like in myotonic dystrophy: a case report |
title | Fundus flavimaculatus-like in myotonic dystrophy: a case report |
title_full | Fundus flavimaculatus-like in myotonic dystrophy: a case report |
title_fullStr | Fundus flavimaculatus-like in myotonic dystrophy: a case report |
title_full_unstemmed | Fundus flavimaculatus-like in myotonic dystrophy: a case report |
title_short | Fundus flavimaculatus-like in myotonic dystrophy: a case report |
title_sort | fundus flavimaculatus-like in myotonic dystrophy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164789/ https://www.ncbi.nlm.nih.gov/pubmed/34051736 http://dx.doi.org/10.1186/s12886-021-02002-5 |
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