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Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up

BACKGROUND: We present a long term follow-up of a young female patient with choroidal infarction, primary open angle glaucoma and Flammer syndrome. The patient had no classical risk factors for vascular occlusions, except for the presence of Flammer syndrome. The essential feature of this syndrome i...

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Autores principales: Terelak-Borys, Barbara, Grabska-Liberek, Iwona, Piekarniak-Wozniak, Anita, Konieczka, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348800/
https://www.ncbi.nlm.nih.gov/pubmed/28288589
http://dx.doi.org/10.1186/s12886-017-0416-4
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author Terelak-Borys, Barbara
Grabska-Liberek, Iwona
Piekarniak-Wozniak, Anita
Konieczka, Katarzyna
author_facet Terelak-Borys, Barbara
Grabska-Liberek, Iwona
Piekarniak-Wozniak, Anita
Konieczka, Katarzyna
author_sort Terelak-Borys, Barbara
collection PubMed
description BACKGROUND: We present a long term follow-up of a young female patient with choroidal infarction, primary open angle glaucoma and Flammer syndrome. The patient had no classical risk factors for vascular occlusions, except for the presence of Flammer syndrome. The essential feature of this syndrome is primary vascular dysregulation, sometimes including vasospasm. The vessels of affected people respond more intensely to a number of stimuli, such as coldness or emotional stress. Any organ can be involved, including parts of the eye. The dense autonomic innervation of the choroidal vessels predisposes them particularly to vasospasms. CASE PRESENTATION: The patient was originally referred to our centre because of a deep unilateral paracentral scotoma with the presumptive diagnosis of a normal tension glaucoma. The discrepancy between the visual field defect and the optic nerve head morphology, however, led us to a vascular evaluation by a simultaneous fluorescein/indocyanine green angiography. This revealed an antecedent choroidal infarction that explained the visual field scotoma and the retinal nerve fibre layer defect in the corresponding area. During the follow-up period of 11 years, the patient also developed bilateral glaucomatous optic neuropathy despite a well-controlled intraocular pressure. CONCLUSIONS: We hypothesise that in the patient presented here, the Flammer syndrome contributed to both the acute unilateral choroidal infarction and to the chronic development of bilateral glaucomatous optic neuropathy.
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spelling pubmed-53488002017-03-14 Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up Terelak-Borys, Barbara Grabska-Liberek, Iwona Piekarniak-Wozniak, Anita Konieczka, Katarzyna BMC Ophthalmol Case Report BACKGROUND: We present a long term follow-up of a young female patient with choroidal infarction, primary open angle glaucoma and Flammer syndrome. The patient had no classical risk factors for vascular occlusions, except for the presence of Flammer syndrome. The essential feature of this syndrome is primary vascular dysregulation, sometimes including vasospasm. The vessels of affected people respond more intensely to a number of stimuli, such as coldness or emotional stress. Any organ can be involved, including parts of the eye. The dense autonomic innervation of the choroidal vessels predisposes them particularly to vasospasms. CASE PRESENTATION: The patient was originally referred to our centre because of a deep unilateral paracentral scotoma with the presumptive diagnosis of a normal tension glaucoma. The discrepancy between the visual field defect and the optic nerve head morphology, however, led us to a vascular evaluation by a simultaneous fluorescein/indocyanine green angiography. This revealed an antecedent choroidal infarction that explained the visual field scotoma and the retinal nerve fibre layer defect in the corresponding area. During the follow-up period of 11 years, the patient also developed bilateral glaucomatous optic neuropathy despite a well-controlled intraocular pressure. CONCLUSIONS: We hypothesise that in the patient presented here, the Flammer syndrome contributed to both the acute unilateral choroidal infarction and to the chronic development of bilateral glaucomatous optic neuropathy. BioMed Central 2017-03-14 /pmc/articles/PMC5348800/ /pubmed/28288589 http://dx.doi.org/10.1186/s12886-017-0416-4 Text en © The Author(s). 2017 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
Terelak-Borys, Barbara
Grabska-Liberek, Iwona
Piekarniak-Wozniak, Anita
Konieczka, Katarzyna
Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up
title Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up
title_full Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up
title_fullStr Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up
title_full_unstemmed Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up
title_short Choroidal infarction in a glaucoma patient with Flammer syndrome: a case report with a long term follow-up
title_sort choroidal infarction in a glaucoma patient with flammer syndrome: a case report with a long term follow-up
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348800/
https://www.ncbi.nlm.nih.gov/pubmed/28288589
http://dx.doi.org/10.1186/s12886-017-0416-4
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