Coats disease mimicking retinoblastoma

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Dolores Ríos y Valles-Valles, MD
Ivette Hernández-Ayuso, MD
Alejandra Lozano Bustillo, MD

Abstract


A 3-year-old girl presented at Asociación para Evitar la Ceguera en México with leukocoria and a blind and painful left eye. Ultrasound revealed a fully occupied vitreous cavity with calcifications and total retinal detachment. Enucleation was performed due to suspected retinoblastoma. Gross findings showed an extensive, yellow, subretinal exudation throughout the vitreous chamber, with the retina displaced anteriorly (A-B). Histopathologically, abundant slit-like cholesterol clefts (arrow head) and foamy histiocytes (arrow) were seen (C), consistent with Coats disease. In addition to these findings, distrophic calcium salts deposits and congenital drusen were identified (D). Coats disease is diagnosed as a different entity in nearly 50% of cases. It is frequently mistaken for retinoblastoma.

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How to Cite
1.
Valles-Valles, MD DR y, Hernández-Ayuso, MD I, Bustillo, MD AL. Coats disease mimicking retinoblastoma. Digit J Ophthalmol. 2022;28(1). Accessed May 4, 2024. https://djo.harvard.edu/index.php/djo/article/view/59
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