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Gliotic opaque posterior hyaloid membrane separation: report of two cases

BACKGROUND: To report two cases with idiopathic unilateral diffuse opacification of the posterior hyaloid membrane (PHM) completely separated from the retina, the mechanism of which is possibly due to glial cell proliferation and migration. CASE PRESENTATION: Two Japanese women at age 75 and 84 with...

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Autores principales: Hosaka, Fumio, Saito, Wataru, Kase, Satoru, Ishida, Susumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381526/
https://www.ncbi.nlm.nih.gov/pubmed/34425785
http://dx.doi.org/10.1186/s12886-021-02072-5
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author Hosaka, Fumio
Saito, Wataru
Kase, Satoru
Ishida, Susumu
author_facet Hosaka, Fumio
Saito, Wataru
Kase, Satoru
Ishida, Susumu
author_sort Hosaka, Fumio
collection PubMed
description BACKGROUND: To report two cases with idiopathic unilateral diffuse opacification of the posterior hyaloid membrane (PHM) completely separated from the retina, the mechanism of which is possibly due to glial cell proliferation and migration. CASE PRESENTATION: Two Japanese women at age 75 and 84 with no systemic or ocular history developed diffuse opacification in one eye resembling a ground glass sheet almost all over the surface of the PHM, but not within the vitreous gel or fluid. The retinas were funduscopically normal; however, optical coherence tomography demonstrated hyperreflective icicle-like anterior protrusions from the surface of the fovea. The patients received pars plana vitrectomy, resulting in visual improvement. Cell block preparations of the vitreous in one case revealed a cluster of cells immunoreactive for glial fibrillary acidic protein in consistence with gliosis, while denying vitreoretinal lymphoma from lack of atypical cells and vitreous amyloidosis due to no staining for Congo red or direct fast scarlet. The lesions did not recur during follow-up with no new funduscopic abnormalities. CONCLUSIONS: To our knowledge, this is the first to demonstrate such peculiar cases of vitreous opacity with idiopathic and unilateral onset. Histological assessments revealed the possible pathogenesis of gliotic opaque PHM separation to cause its ground-glass-sheet appearance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-021-02072-5.
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spelling pubmed-83815262021-08-23 Gliotic opaque posterior hyaloid membrane separation: report of two cases Hosaka, Fumio Saito, Wataru Kase, Satoru Ishida, Susumu BMC Ophthalmol Case Report BACKGROUND: To report two cases with idiopathic unilateral diffuse opacification of the posterior hyaloid membrane (PHM) completely separated from the retina, the mechanism of which is possibly due to glial cell proliferation and migration. CASE PRESENTATION: Two Japanese women at age 75 and 84 with no systemic or ocular history developed diffuse opacification in one eye resembling a ground glass sheet almost all over the surface of the PHM, but not within the vitreous gel or fluid. The retinas were funduscopically normal; however, optical coherence tomography demonstrated hyperreflective icicle-like anterior protrusions from the surface of the fovea. The patients received pars plana vitrectomy, resulting in visual improvement. Cell block preparations of the vitreous in one case revealed a cluster of cells immunoreactive for glial fibrillary acidic protein in consistence with gliosis, while denying vitreoretinal lymphoma from lack of atypical cells and vitreous amyloidosis due to no staining for Congo red or direct fast scarlet. The lesions did not recur during follow-up with no new funduscopic abnormalities. CONCLUSIONS: To our knowledge, this is the first to demonstrate such peculiar cases of vitreous opacity with idiopathic and unilateral onset. Histological assessments revealed the possible pathogenesis of gliotic opaque PHM separation to cause its ground-glass-sheet appearance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-021-02072-5. BioMed Central 2021-08-23 /pmc/articles/PMC8381526/ /pubmed/34425785 http://dx.doi.org/10.1186/s12886-021-02072-5 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
Hosaka, Fumio
Saito, Wataru
Kase, Satoru
Ishida, Susumu
Gliotic opaque posterior hyaloid membrane separation: report of two cases
title Gliotic opaque posterior hyaloid membrane separation: report of two cases
title_full Gliotic opaque posterior hyaloid membrane separation: report of two cases
title_fullStr Gliotic opaque posterior hyaloid membrane separation: report of two cases
title_full_unstemmed Gliotic opaque posterior hyaloid membrane separation: report of two cases
title_short Gliotic opaque posterior hyaloid membrane separation: report of two cases
title_sort gliotic opaque posterior hyaloid membrane separation: report of two cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381526/
https://www.ncbi.nlm.nih.gov/pubmed/34425785
http://dx.doi.org/10.1186/s12886-021-02072-5
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