Literature DB >> 24366775

Solitary congenital hypertrophy of the retinal pigment epithelium features by high-definition optical coherence tomography.

Javier Orduña-Azcona1, Pablo Gili, Sofia De Manuel-Triantafilo, Patricia Flores-Rodriguez.   

Abstract

PURPOSE: To describe the features of solitary congenital hypertrophy of the retinal pigment epithelium (CHRPE) using high-definition optical coherence tomography (HD-OCT).
METHODS: This was a retrospective, observational, noncomparative case series including 16 consecutive patients with solitary CHRPE. We describe the clinical and OCT features of CHRPE using the 5 radial lines acquisition OCT protocol over the CHRPE and the retina next to the tumor.
RESULTS: The mean patient age was 54 years (median 57 years; range 8-76 years). The CHRPE lesion was outside the posterior pole in 14 of the patients (8 temporal, 3 superior, 2 nasal, and 1 inferior quadrant) and 2 peripapillary. Fifteen patients (94%) showed retinal thinning and complete photoreceptor loss overlying the CHRPE. The RPE hyperreflectivity was found in all patients. The retina over the lesion measured a mean of 60.3% (range 41%-95%) of the thickness of the adjacent normal retina.
CONCLUSIONS: High-definition OCT showed retinal thinning, photoreceptor loss, and RPE hyperreflectivity in solitary CHRPE lesions.

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Year:  2013        PMID: 24366775     DOI: 10.5301/ejo.5000420

Source DB:  PubMed          Journal:  Eur J Ophthalmol        ISSN: 1120-6721            Impact factor:   2.597


  1 in total

1.  Optical Coherence Tomography Characteristics of the Choroid Underlying Congenital Hypertrophy of the Retinal Pigment Epithelium.

Authors:  Jasmine H Francis; Ethan K Sobol; Molly Greenberg; Robert Folberg; David H Abramson
Journal:  Ocul Oncol Pathol       Date:  2020-02-27
  1 in total

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