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Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report

INTRODUCTION: To report a case of unilateral peripheral cone dysfunction syndrome and evaluate the associated clinicopathological changes using swept-source optical coherence tomography (SS-OCT). CASE PRESENTATION: A 39-year-old Japanese woman reported a visual field defect of 2-years duration in th...

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Autores principales: Hasegawa, Tetsuya, Tetsuka, Soichi, Yamaguchi, Aya, Kobashi, Chieko, Sato, Tomomi, Tanaka, Yoshiaki, Kakehashi, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524220/
https://www.ncbi.nlm.nih.gov/pubmed/31096954
http://dx.doi.org/10.1186/s12886-019-1121-2
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author Hasegawa, Tetsuya
Tetsuka, Soichi
Yamaguchi, Aya
Kobashi, Chieko
Sato, Tomomi
Tanaka, Yoshiaki
Kakehashi, Akihiro
author_facet Hasegawa, Tetsuya
Tetsuka, Soichi
Yamaguchi, Aya
Kobashi, Chieko
Sato, Tomomi
Tanaka, Yoshiaki
Kakehashi, Akihiro
author_sort Hasegawa, Tetsuya
collection PubMed
description INTRODUCTION: To report a case of unilateral peripheral cone dysfunction syndrome and evaluate the associated clinicopathological changes using swept-source optical coherence tomography (SS-OCT). CASE PRESENTATION: A 39-year-old Japanese woman reported a visual field defect of 2-years duration in the right eye. The patient underwent visual field testing, full-field electroretinography (ff-ERG), SS-OCT, and a routine ophthalmologic examination. The best-corrected visual acuity was 20/20 bilaterally. The funduscopy examination was normal bilaterally. Visual field testing showed a relative paracentral scotoma in the right eye. SS-OCT scans showed an unclear interdigitation zone (IZ) throughout the posterior pole except for the foveal zone in the right eye. SS-OCT macular analysis showed thinning of the ganglion cell layer (GCL) and inner plexiform layer (IPL) corresponding to the region of the IZ defect. ff-ERG showed almost normal flash ERGs and normal rod responses bilaterally. The cone response and flicker ERG response were decreased markedly only in the right eye. CONCLUSION: To the best of our knowledge, this is the first case report of unilateral peripheral cone dysfunction syndrome in which SS-OCT showed pathological changes in the GCL and IPL. The OCT findings corresponded well to the ERG changes and visual field abnormality. Because foveolar cone photoreceptor cells are connected in a one-to-one correspondence to retinal ganglion cells without connection to the horizontal cells or amacrine cells, the GCL and IPL were not present in the fovea. Based on this analysis, we speculated that the primary lesion of peripheral cone dysfunction syndrome is not in the cone photoreceptor cells but in the horizontal cells and/or amacrine cells. The clinicopathological changes in the ganglion cells and cone photoreceptor cells might be the subsequent pathologies in the horizontal cells in peripheral cone dysfunction syndrome.
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spelling pubmed-65242202019-05-24 Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report Hasegawa, Tetsuya Tetsuka, Soichi Yamaguchi, Aya Kobashi, Chieko Sato, Tomomi Tanaka, Yoshiaki Kakehashi, Akihiro BMC Ophthalmol Case Report INTRODUCTION: To report a case of unilateral peripheral cone dysfunction syndrome and evaluate the associated clinicopathological changes using swept-source optical coherence tomography (SS-OCT). CASE PRESENTATION: A 39-year-old Japanese woman reported a visual field defect of 2-years duration in the right eye. The patient underwent visual field testing, full-field electroretinography (ff-ERG), SS-OCT, and a routine ophthalmologic examination. The best-corrected visual acuity was 20/20 bilaterally. The funduscopy examination was normal bilaterally. Visual field testing showed a relative paracentral scotoma in the right eye. SS-OCT scans showed an unclear interdigitation zone (IZ) throughout the posterior pole except for the foveal zone in the right eye. SS-OCT macular analysis showed thinning of the ganglion cell layer (GCL) and inner plexiform layer (IPL) corresponding to the region of the IZ defect. ff-ERG showed almost normal flash ERGs and normal rod responses bilaterally. The cone response and flicker ERG response were decreased markedly only in the right eye. CONCLUSION: To the best of our knowledge, this is the first case report of unilateral peripheral cone dysfunction syndrome in which SS-OCT showed pathological changes in the GCL and IPL. The OCT findings corresponded well to the ERG changes and visual field abnormality. Because foveolar cone photoreceptor cells are connected in a one-to-one correspondence to retinal ganglion cells without connection to the horizontal cells or amacrine cells, the GCL and IPL were not present in the fovea. Based on this analysis, we speculated that the primary lesion of peripheral cone dysfunction syndrome is not in the cone photoreceptor cells but in the horizontal cells and/or amacrine cells. The clinicopathological changes in the ganglion cells and cone photoreceptor cells might be the subsequent pathologies in the horizontal cells in peripheral cone dysfunction syndrome. BioMed Central 2019-05-16 /pmc/articles/PMC6524220/ /pubmed/31096954 http://dx.doi.org/10.1186/s12886-019-1121-2 Text en © The Author(s). 2019 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
Hasegawa, Tetsuya
Tetsuka, Soichi
Yamaguchi, Aya
Kobashi, Chieko
Sato, Tomomi
Tanaka, Yoshiaki
Kakehashi, Akihiro
Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report
title Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report
title_full Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report
title_fullStr Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report
title_full_unstemmed Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report
title_short Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report
title_sort optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524220/
https://www.ncbi.nlm.nih.gov/pubmed/31096954
http://dx.doi.org/10.1186/s12886-019-1121-2
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