| Literature DB >> 32002404 |
Basil K Williams1,2, Maura Di Nicola1,2, J Antonio Lucio-Alvarez1,3, David R Lally4, Carol L Shields1.
Abstract
Neoplasms of the retinal pigment epithelium (RPE) are rare tumors that can simulate choroidal melanoma, but clinical and imaging characteristics often differentiate these lesions. We report a 70-year-old male with an abruptly elevated pigmented lesion that arose at the site of congenital hypertrophy of the RPE and demonstrated associated exudation, as well as feeding and draining vessels, suggestive of RPE adenoma. Optical coherence tomography showed retinal elevation with serous retinal detachment adjacent to the mass, and ultrasonography revealed an abruptly elevated, moderately echodense mass of 6.4-mm thickness. Fluorescein -angiography showed early tumor hypofluorescence, late -tumor hyperfluorescence with staining and leakage, and -retinal vessels buried under the mass, suggestive of a retinal tumor. The patient was monitored with the presumed diagnosis of RPE adenoma, but 3 months later, the growth was documented and fine-needle aspiration biopsy revealed choroidal melanoma. Management with I-125 plaque radiotherapy was performed leading to tumor regression and a thickness of 4.6 mm.Entities:
Keywords: Choroidal melanoma; Congenital hypertrophy of the retinal pigment epithelium; Malignant melanoma; Retinal pigment epithelium adenoma
Year: 2019 PMID: 32002404 PMCID: PMC6984159 DOI: 10.1159/000501084
Source DB: PubMed Journal: Ocul Oncol Pathol ISSN: 2296-4657