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International Ophthalmology

, Volume 39, Issue 2, pp 441–444 | Cite as

Choroidal osteoma and pattern dystrophy of retinal pigment epithelium

  • Vinod KumarEmail author
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Abstract

Purpose

To describe co-occurrence of choroidal osteoma in a patient with pattern dystrophy of retinal pigment epithelium.

Methods

Clinical case report

Results

A young female presented with decreased vision in the right eye due to decalcification of choroidal osteoma. Multimodal imaging including fundus autofluorescence, fluorescein angiography and optical coherence tomography showed features of pattern dystrophy of retinal pigment epithelium that simulates the Stargardt disease.

Conclusions

This co-occurrence of choroidal osteoma and pattern dystrophy is likely to be incidental. Multimodal imaging may help in differentiating pattern dystrophy of retinal pigment epithelium that simulates Stargardt disease from Stargardt disease.

Keywords

Choroidal osteoma Pattern dystrophy Retinal pigment epithelium Multimodal imaging 

Notes

Compliance with ethical standards

Conflict of interest

The author declares that he has no conflict of interest.

Ethical approval

All procedures performed in this report were in accordance with the institutional guidelines and with the 1964 Helsinki Declaration and its later amendments.

Informed consent

Informed consent was obtained.

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Copyright information

© Springer Science+Business Media B.V., part of Springer Nature 2017

Authors and Affiliations

  1. 1.Dr Rajendra Prasad Centre for Ophthalmic SciencesAll India Institute of Medical SciencesNew DelhiIndia

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