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Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma
BACKGROUND: To describe a unique case of decompression retinopathy manifesting as pre-macular subhyaloid hemorrhage that occurs in a nine-day old child after undergoing a non-penetrating deep sclerectomy for primary congenital glaucoma. CASE PRESENTATION: We report a single case of a 9-day-old boy w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126034/ https://www.ncbi.nlm.nih.gov/pubmed/30185152 http://dx.doi.org/10.1186/s12886-018-0906-z |
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author | Ramtohul, Prithvi Chardavoine, Maëva Beylerian, Marie Aziz, Aurore Matonti, Frédéric Denis, Danièle |
author_facet | Ramtohul, Prithvi Chardavoine, Maëva Beylerian, Marie Aziz, Aurore Matonti, Frédéric Denis, Danièle |
author_sort | Ramtohul, Prithvi |
collection | PubMed |
description | BACKGROUND: To describe a unique case of decompression retinopathy manifesting as pre-macular subhyaloid hemorrhage that occurs in a nine-day old child after undergoing a non-penetrating deep sclerectomy for primary congenital glaucoma. CASE PRESENTATION: We report a single case of a 9-day-old boy who was referred to our department of ophthalmology for bilateral buphtalmia and corneal edema. He presented marked elevation of the intraocular pressure in both eyes (22 mmHg and 26 mmHg, in the right eye and left eye respectively) associated with significant optic nerve cupping. Non-penetrating deep sclerectomy was performed for each eye, with effective reduction of the intraocular pressure during the first week postoperatively (11 mmHg and 7 mmHg in the right eye and left eye respectively). The right eye presented an isolated subhyaloid hemorrhage located in the pre-macular area, persisting 3 weeks after the initial surgery and requiring pars-plana vitrectomy to clear the visual axis. This uncommon complication was identified as decompression retinopathy. The intraocular pressure remained controlled in the normal range three years after initial surgery in both eyes, with reversal of optic disc cupping. CONCLUSIONS: Decompression retinopathy is a potential complication after non-penetrating deep sclerectomy in primary congenital glaucoma, requiring prompt treatment strategy to prevent potential organic amblyopia. |
format | Online Article Text |
id | pubmed-6126034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61260342018-09-10 Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma Ramtohul, Prithvi Chardavoine, Maëva Beylerian, Marie Aziz, Aurore Matonti, Frédéric Denis, Danièle BMC Ophthalmol Case Report BACKGROUND: To describe a unique case of decompression retinopathy manifesting as pre-macular subhyaloid hemorrhage that occurs in a nine-day old child after undergoing a non-penetrating deep sclerectomy for primary congenital glaucoma. CASE PRESENTATION: We report a single case of a 9-day-old boy who was referred to our department of ophthalmology for bilateral buphtalmia and corneal edema. He presented marked elevation of the intraocular pressure in both eyes (22 mmHg and 26 mmHg, in the right eye and left eye respectively) associated with significant optic nerve cupping. Non-penetrating deep sclerectomy was performed for each eye, with effective reduction of the intraocular pressure during the first week postoperatively (11 mmHg and 7 mmHg in the right eye and left eye respectively). The right eye presented an isolated subhyaloid hemorrhage located in the pre-macular area, persisting 3 weeks after the initial surgery and requiring pars-plana vitrectomy to clear the visual axis. This uncommon complication was identified as decompression retinopathy. The intraocular pressure remained controlled in the normal range three years after initial surgery in both eyes, with reversal of optic disc cupping. CONCLUSIONS: Decompression retinopathy is a potential complication after non-penetrating deep sclerectomy in primary congenital glaucoma, requiring prompt treatment strategy to prevent potential organic amblyopia. BioMed Central 2018-09-05 /pmc/articles/PMC6126034/ /pubmed/30185152 http://dx.doi.org/10.1186/s12886-018-0906-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Ramtohul, Prithvi Chardavoine, Maëva Beylerian, Marie Aziz, Aurore Matonti, Frédéric Denis, Danièle Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma |
title | Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma |
title_full | Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma |
title_fullStr | Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma |
title_full_unstemmed | Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma |
title_short | Decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma |
title_sort | decompression retinopathy following nonpenetrating deep sclerectomy for primary congenital glaucoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126034/ https://www.ncbi.nlm.nih.gov/pubmed/30185152 http://dx.doi.org/10.1186/s12886-018-0906-z |
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