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Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium
AIMS: To investigate age-related lesions in the far-anterior retina that migrate from the ciliary body (CB) and how they affect the neural retina and retinal pigmented epithelium (RPE). METHODS: One eye from three healthy subjects aged 87, 92 and 93 years were used. Retinae were photographed, embedd...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355342/ https://www.ncbi.nlm.nih.gov/pubmed/22426947 http://dx.doi.org/10.1136/bjophthalmol-2011-301273 |
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author | Begum, Rana Jeffery, Glen |
author_facet | Begum, Rana Jeffery, Glen |
author_sort | Begum, Rana |
collection | PubMed |
description | AIMS: To investigate age-related lesions in the far-anterior retina that migrate from the ciliary body (CB) and how they affect the neural retina and retinal pigmented epithelium (RPE). METHODS: One eye from three healthy subjects aged 87, 92 and 93 years were used. Retinae were photographed, embedded in resin and then sectioned at 2 μm. RESULTS: Multiple elliptically shaped lesions were present in the CB. Larger lesions extended into the peripheral retina. Lesions resulted from deposits that had lenticular qualities. These develop centrally along Bruch's membrane sweeping away the RPE, such that piles of RPE cells were present around the deposits that resulted in retinal atrophy. The internal composition of the deposits revealed large numbers of spherical bodies, unlike those seen in drusen. RPE cells adjacent to these deposits and their underlying lesions became highly irregular, with melanin granules spacing themselves out within the cell and adopting similar orientations. This is a highly distinctive feature. CONCLUSIONS: These far-anterior deposits were different in nature from drusen in terms of morphology, composition and origin. They swept away the RPE, exposing the Bruch's membrane and isolating the retina, leading to atrophy. They appeared to originate from the CB and progressed centrally. The deposits may have developed from the ciliary muscle, which would account for their elongated orientation. Their impact on melanin distribution in RPE cells was unexpected and unusual, implying that they release a signal that influences melanin organisation. |
format | Online Article Text |
id | pubmed-3355342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BMJ Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33553422012-05-18 Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium Begum, Rana Jeffery, Glen Br J Ophthalmol Laboratory Science AIMS: To investigate age-related lesions in the far-anterior retina that migrate from the ciliary body (CB) and how they affect the neural retina and retinal pigmented epithelium (RPE). METHODS: One eye from three healthy subjects aged 87, 92 and 93 years were used. Retinae were photographed, embedded in resin and then sectioned at 2 μm. RESULTS: Multiple elliptically shaped lesions were present in the CB. Larger lesions extended into the peripheral retina. Lesions resulted from deposits that had lenticular qualities. These develop centrally along Bruch's membrane sweeping away the RPE, such that piles of RPE cells were present around the deposits that resulted in retinal atrophy. The internal composition of the deposits revealed large numbers of spherical bodies, unlike those seen in drusen. RPE cells adjacent to these deposits and their underlying lesions became highly irregular, with melanin granules spacing themselves out within the cell and adopting similar orientations. This is a highly distinctive feature. CONCLUSIONS: These far-anterior deposits were different in nature from drusen in terms of morphology, composition and origin. They swept away the RPE, exposing the Bruch's membrane and isolating the retina, leading to atrophy. They appeared to originate from the CB and progressed centrally. The deposits may have developed from the ciliary muscle, which would account for their elongated orientation. Their impact on melanin distribution in RPE cells was unexpected and unusual, implying that they release a signal that influences melanin organisation. BMJ Group 2012-03-18 2012-06 /pmc/articles/PMC3355342/ /pubmed/22426947 http://dx.doi.org/10.1136/bjophthalmol-2011-301273 Text en © 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Laboratory Science Begum, Rana Jeffery, Glen Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium |
title | Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium |
title_full | Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium |
title_fullStr | Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium |
title_full_unstemmed | Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium |
title_short | Aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium |
title_sort | aged peripheral retinal lesions originating from the ciliary body sweep away the retinal pigmented epithelium |
topic | Laboratory Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355342/ https://www.ncbi.nlm.nih.gov/pubmed/22426947 http://dx.doi.org/10.1136/bjophthalmol-2011-301273 |
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