An atypical case of retinal pigment epithelium tear with remodeling and visual preservation

This report describes a patient with polypoidal choroidal vasculopathy (PCV) with fovea-involving retinal pigment epithelium (RPE) tear that showed tissue remodeling with a good visual outcome. Imaging over the patient’s clinical course from 2019 was reviewed. A 74-year-old female presented with lef...

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Main Authors: Charles Jit Teng Ong, Chui Ming Gemmy Cheung
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:Taiwan Journal of Ophthalmology
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Online Access:https://journals.lww.com/10.4103/tjo.TJO-D-24-00051
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author Charles Jit Teng Ong
Chui Ming Gemmy Cheung
author_facet Charles Jit Teng Ong
Chui Ming Gemmy Cheung
author_sort Charles Jit Teng Ong
collection DOAJ
description This report describes a patient with polypoidal choroidal vasculopathy (PCV) with fovea-involving retinal pigment epithelium (RPE) tear that showed tissue remodeling with a good visual outcome. Imaging over the patient’s clinical course from 2019 was reviewed. A 74-year-old female presented with left submacular hemorrhage and a large multi-lobular pigment epithelial detachment. Left eye vision was 6/19 at the presentation. Indocyanine green angiography (ICGA) revealed underlying PCV. One month after initiation of intravitreal aflibercept (IVA, Bayer), she developed fresh subretinal hemorrhage. An RPE tear of 1 disc area in size, centered over the fovea was diagnosed. The torn RPE edge was scrolled up temporal to the fovea on spectral-domain optical coherence tomography (SD-OCT), with hypertransmission into the choroid observed over the area of RPE loss. Left eye vision after the RPE tear was 6/15. Over the next 2 months, the subretinal hemorrhage resolved following further IVA. At month 3, fundus autofluorescence (FAF) demonstrated hypo-autofluorescence while fundus fluorescein angiography (FFA) and ICGA showed a window defect corresponding to the area of RPE tear. On SD-OCT, there was a faint hyper-reflective layer where one might expect the RPE layer to be. Serial SD-OCT scans over 5 years revealed increasing prominence of the hyperreflective layer between the ellipsoid zone and Bruch’s membrane. FAF remained hypo-autofluorescent. At the last review, the patient retained 6/9 vision. We report a case of fovea-involving RPE tear documented with multimodal imaging with good visual outcome, which is atypical. Serial OCT suggests tissue remodeling may explain the functional preservation.
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spelling doaj-art-c62172e7d48842c18ebb2db5b94dd8f22025-01-14T15:51:54ZengWolters Kluwer Medknow PublicationsTaiwan Journal of Ophthalmology2211-50562211-50722024-12-0114461461810.4103/tjo.TJO-D-24-00051An atypical case of retinal pigment epithelium tear with remodeling and visual preservationCharles Jit Teng OngChui Ming Gemmy CheungThis report describes a patient with polypoidal choroidal vasculopathy (PCV) with fovea-involving retinal pigment epithelium (RPE) tear that showed tissue remodeling with a good visual outcome. Imaging over the patient’s clinical course from 2019 was reviewed. A 74-year-old female presented with left submacular hemorrhage and a large multi-lobular pigment epithelial detachment. Left eye vision was 6/19 at the presentation. Indocyanine green angiography (ICGA) revealed underlying PCV. One month after initiation of intravitreal aflibercept (IVA, Bayer), she developed fresh subretinal hemorrhage. An RPE tear of 1 disc area in size, centered over the fovea was diagnosed. The torn RPE edge was scrolled up temporal to the fovea on spectral-domain optical coherence tomography (SD-OCT), with hypertransmission into the choroid observed over the area of RPE loss. Left eye vision after the RPE tear was 6/15. Over the next 2 months, the subretinal hemorrhage resolved following further IVA. At month 3, fundus autofluorescence (FAF) demonstrated hypo-autofluorescence while fundus fluorescein angiography (FFA) and ICGA showed a window defect corresponding to the area of RPE tear. On SD-OCT, there was a faint hyper-reflective layer where one might expect the RPE layer to be. Serial SD-OCT scans over 5 years revealed increasing prominence of the hyperreflective layer between the ellipsoid zone and Bruch’s membrane. FAF remained hypo-autofluorescent. At the last review, the patient retained 6/9 vision. We report a case of fovea-involving RPE tear documented with multimodal imaging with good visual outcome, which is atypical. Serial OCT suggests tissue remodeling may explain the functional preservation.https://journals.lww.com/10.4103/tjo.TJO-D-24-00051polypoidal choroidal vasculopathyage-related macular degenerationretinal pigment epitheliumretinal pigment epithelium teartissue remodelingmultimodal imaging
spellingShingle Charles Jit Teng Ong
Chui Ming Gemmy Cheung
An atypical case of retinal pigment epithelium tear with remodeling and visual preservation
Taiwan Journal of Ophthalmology
polypoidal choroidal vasculopathy
age-related macular degeneration
retinal pigment epithelium
retinal pigment epithelium tear
tissue remodeling
multimodal imaging
title An atypical case of retinal pigment epithelium tear with remodeling and visual preservation
title_full An atypical case of retinal pigment epithelium tear with remodeling and visual preservation
title_fullStr An atypical case of retinal pigment epithelium tear with remodeling and visual preservation
title_full_unstemmed An atypical case of retinal pigment epithelium tear with remodeling and visual preservation
title_short An atypical case of retinal pigment epithelium tear with remodeling and visual preservation
title_sort atypical case of retinal pigment epithelium tear with remodeling and visual preservation
topic polypoidal choroidal vasculopathy
age-related macular degeneration
retinal pigment epithelium
retinal pigment epithelium tear
tissue remodeling
multimodal imaging
url https://journals.lww.com/10.4103/tjo.TJO-D-24-00051
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