Evidence map›Paper›PMID 42541042›Full record

ArticleOcular oncology and pathology2026

Optical Coherence Tomography Features and Multimodal Imaging Findings in Choroidal Osteoma: A Case Series.

Selda Celik Dulger, Furkan Emre Söğüt, Mehmet Yasin Teke, Mehmet Citirik

Abstract read
In one paragraph

Article in Ocular oncology and pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Selda Celik DulgerDepartment of Ophthalmology, Ministry of Health Ankara Etlik City Hospital, Ankara, Turkey.
Furkan Emre SöğütDepartment of Ophthalmology, Cubuk Halil Şıvgın State Hospital, Ankara, Turkey.
Mehmet Yasin TekeDepartment of Ophthalmology, Ministry of Health Ankara Etlik City Hospital, Ankara, Turkey.
Mehmet CitirikDepartment of Ophthalmology, Ministry of Health Ankara Etlik City Hospital, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The aim of this study was to characterize optical coherence tomography (OCT) findings in choroidal osteoma and evaluate their associations with subretinal fluid, choroidal neovascularization, and structural retinal changes. Methods: This retrospective descriptive case series included 7 patients (10 eyes) with choroidal osteoma evaluated at a tertiary referral center. All eyes underwent comprehensive ophthalmologic examination and spectral-domain OCT imaging. OCT scans were analyzed for predefined structural features, including hyperreflective lamellar patterns, spongiform appearance, outer retinal alterations, and subretinal fluid. Subretinal fluid was classified as neovascular or non-neovascular based on OCT characteristics. Results: OCT revealed marked structural heterogeneity. Three eyes demonstrated isolated subretinal fluid without neovascular features, resolving spontaneously in two cases. Three eyes showed chronic subretinal fluid or intraretinal cystic changes with neovascular OCT features and responded favorably to repeated intravitreal anti-vascular endothelial growth factor therapy. One eye with long-term follow-up exhibited progressive tumor decalcification with severe retinal and choroidal thinning and poor visual outcome. Focal choroidal excavation was identified in one eye in association with choroidal neovascularization. Conclusion: Choroidal osteoma exhibits heterogeneous OCT patterns reflecting different mechanisms of visual impairment. Careful OCT-based assessment may aid differentiation of neovascular and non-neovascular changes and guide clinical management.

Indexed as

Choroidal neovascularizationChoroidal osteomaOptical coherence tomographyRetinal structural changesSubretinal fluid

Identifiers

PMID42541042
PMCPMC13427355

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.