A case of acute retinal pigment epithelitis: spectral domain optical coherence tomography time course and physiopathologic hypothesis.

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Etat: Public
Version: Final published version
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ID Serval
serval:BIB_FAB2C2540E6C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A case of acute retinal pigment epithelitis: spectral domain optical coherence tomography time course and physiopathologic hypothesis.
Périodique
Clinical Ophthalmology (auckland, N.z.)
Auteur⸱e⸱s
Puche N., Offret O., Bernard J.A., Behar-Cohen F.
ISSN
1177-5483 (Electronic)
ISSN-L
1177-5467
Statut éditorial
Publié
Date de publication
2010
Peer-reviewed
Oui
Volume
4
Pages
1029-1033
Langue
anglais
Notes
Publication types: Journal Article Publication Status: epublish
Résumé
PURPOSE: To report the time course of retinal morphologic changes in a patient with acute retinal pigment epithelitis (ARPE) using spectral domain optical coherence tomography (SD-OCT).
METHODS: A 30-year old man was referred for blurred vision of his right eye after five days that appeared suddenly 15 days after recovery from a flu-like syndrome. SD-OCT was performed immediately, followed by fluorescein and infracyanine angiography at eight days and then at three weeks.
RESULTS: At presentation, a bubble of sub-macular deposit was observed on the right macula with central golden micronodules in a honeycomb pattern. SD-OCT showed an "anterior dislocation" of all the retinal layers up to the inner/outer segment (IS/OS) line and irregular deposits at the OS level together with thickening of the retinal pigment epithelial (RPE) layer. As visual acuity increased, eight days later, the OCT showed reduction of the sub-retinal deposits and an abnormal hyperflectivity of the sub-retinal and RPE layers was observed. The patient showed a positive serology for picornavirus.
DISCUSSION: The acute SD-OCT sections of this patient with ARPE were compared with histological sections of a 35 day old Royal College of Surgeons rat. Similar findings could be observed, with preservation of the IS/OS line and accumulation of debris at the OS level, suggesting that ARPE symptoms could result from a transient phagocytic dysfunction of the RPE at the fovea, inducing reversible accumulation of undigested OS. Picornaviruses comprising enterovirus and coxsachievirus described as being associated with acute chorioretinitis. In this case, it was responsible for ARPE.
CONCLUSION: We hypothesize that ARPE syndrome results from a transient dysfunction of RPE, which can occur as a post viral reaction.
Pubmed
Création de la notice
23/08/2013 8:26
Dernière modification de la notice
20/08/2019 17:26
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