ArticleTherapeutic advances in ophthalmology
Spontaneous resolution of optic pit maculopathy: an OCT report.
Article in Therapeutic advances in ophthalmology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 8 citations in OpenAlex.
- Retinal detachment complicating ocular coloboma.Eye (London, England) · 2026Review
- Corneal stromal lenticule transplantation for the treatment of congenital optic disc pit maculopathy : a case report and review.BMC ophthalmology · 2024Review
- Congenital optic disc pits and optic disc pit maculopathy: a review.Frontiers in ophthalmology · 2023Review
- Optic Pit Maculopathy: Clinical Features and Management Options.Current ophthalmology reports · 2021Article
- Resolution of Optic Disc Pit Maculopathy Following Posterior Vitreous Detachment.Journal of vitreoretinal diseasesArticle
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Authors and funding
8 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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.
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