Spontaneous resolution of optic pit maculopathy: an OCT report

The separation of the vitreous from the optic nerve head and the macula plays a primary role in the spontaneous resolution of optic disc pit (ODP) maculopathy. Optical coherence tomography (OCT) helps in the non-invasive monitoring of this condition, when treated conservatively. The aim of this repo...

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Main Authors: Massimo Lorusso, Roberta Zito, Luisa Micelli Ferrari, Eleni Nikolopoulou, Maria Vittoria Cicinelli, Enrico Borrelli, Giuseppe Querques, Tommaso Micelli Ferrari
Format: Article
Language:English
Published: SAGE Publishing 2020-08-01
Series:Therapeutic Advances in Ophthalmology
Online Access:https://doi.org/10.1177/2515841420950843
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spelling doaj-34e5338c2a5b4e3eb6097915307b277f2020-11-25T04:01:11ZengSAGE PublishingTherapeutic Advances in Ophthalmology2515-84142020-08-011210.1177/2515841420950843Spontaneous resolution of optic pit maculopathy: an OCT reportMassimo LorussoRoberta ZitoLuisa Micelli FerrariEleni NikolopoulouMaria Vittoria CicinelliEnrico BorrelliGiuseppe QuerquesTommaso Micelli FerrariThe separation of the vitreous from the optic nerve head and the macula plays a primary role in the spontaneous resolution of optic disc pit (ODP) maculopathy. Optical coherence tomography (OCT) helps in the non-invasive monitoring of this condition, when treated conservatively. The aim of this report was to describe a pediatric case of spontaneously resolved ODP maculopathy, managed conservatively and monitored by means of spectral domain (SD)-OCT. A 14-year-old girl presented with severe visual loss in the right eye (RE). Fundus examination demonstrated a temporal ODP with altered foveal reflex. The SD-OCT B-scans revealed severe intraretinal schisis-like changes, broad vitreal adhesion in the optic nerve head area, posterior hyaloid thickening, and vitreal entrapment in the premacular space. The patient was managed conservatively. Spontaneous resolution of ODP maculopathy took place over 3 months, with vision improved up to 1.0 (Snellen charts). The macular schisis progressively resolved after posterior vitreous detachment. In conclusion, in our report, a complete restoration of the foveal anatomy was achieved without any surgical intervention. This OCT-based report confirms the role of the vitreomacular abnormalities in the pathogenesis of the disease.https://doi.org/10.1177/2515841420950843
collection DOAJ
language English
format Article
sources DOAJ
author Massimo Lorusso
Roberta Zito
Luisa Micelli Ferrari
Eleni Nikolopoulou
Maria Vittoria Cicinelli
Enrico Borrelli
Giuseppe Querques
Tommaso Micelli Ferrari
spellingShingle Massimo Lorusso
Roberta Zito
Luisa Micelli Ferrari
Eleni Nikolopoulou
Maria Vittoria Cicinelli
Enrico Borrelli
Giuseppe Querques
Tommaso Micelli Ferrari
Spontaneous resolution of optic pit maculopathy: an OCT report
Therapeutic Advances in Ophthalmology
author_facet Massimo Lorusso
Roberta Zito
Luisa Micelli Ferrari
Eleni Nikolopoulou
Maria Vittoria Cicinelli
Enrico Borrelli
Giuseppe Querques
Tommaso Micelli Ferrari
author_sort Massimo Lorusso
title Spontaneous resolution of optic pit maculopathy: an OCT report
title_short Spontaneous resolution of optic pit maculopathy: an OCT report
title_full Spontaneous resolution of optic pit maculopathy: an OCT report
title_fullStr Spontaneous resolution of optic pit maculopathy: an OCT report
title_full_unstemmed Spontaneous resolution of optic pit maculopathy: an OCT report
title_sort spontaneous resolution of optic pit maculopathy: an oct report
publisher SAGE Publishing
series Therapeutic Advances in Ophthalmology
issn 2515-8414
publishDate 2020-08-01
description The separation of the vitreous from the optic nerve head and the macula plays a primary role in the spontaneous resolution of optic disc pit (ODP) maculopathy. Optical coherence tomography (OCT) helps in the non-invasive monitoring of this condition, when treated conservatively. The aim of this report was to describe a pediatric case of spontaneously resolved ODP maculopathy, managed conservatively and monitored by means of spectral domain (SD)-OCT. A 14-year-old girl presented with severe visual loss in the right eye (RE). Fundus examination demonstrated a temporal ODP with altered foveal reflex. The SD-OCT B-scans revealed severe intraretinal schisis-like changes, broad vitreal adhesion in the optic nerve head area, posterior hyaloid thickening, and vitreal entrapment in the premacular space. The patient was managed conservatively. Spontaneous resolution of ODP maculopathy took place over 3 months, with vision improved up to 1.0 (Snellen charts). The macular schisis progressively resolved after posterior vitreous detachment. In conclusion, in our report, a complete restoration of the foveal anatomy was achieved without any surgical intervention. This OCT-based report confirms the role of the vitreomacular abnormalities in the pathogenesis of the disease.
url https://doi.org/10.1177/2515841420950843
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