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Unilateral Xanthocoria and Retinal Vascular Anomalies in a 3-Year-Old Boy: Retinoblastoma or Coats Disease?

Authors :
Ahmad S
Azarcon CP
Hubbard GB
Wells JR
Source :
Journal of pediatric ophthalmology and strabismus [J Pediatr Ophthalmol Strabismus] 2022 May-Jun; Vol. 59 (3), pp. e33-e34. Date of Electronic Publication: 2022 May 01.
Publication Year :
2022

Abstract

The authors describe a challenging case of unilateral retinoblastoma in a patient referred for xanthocoria. A 3-year-old boy was referred for unilateral xanthocoria and disordered retinal vasculature, suggestive of Coats disease. Further investigation revealed diffuse subretinal tumor seeding and areas of calcification, consistent with retinoblastoma. Enucleation was performed and histopathology confirmed exophytic retinoblastoma. This case highlights that xanthocoria, although often encountered in patients with Coats disease, can sometimes be associated with retinoblastoma. As such, retinoblastoma should be considered in the differential diagnosis for children with both leukocoria and xanthocoria. [ J Pediatr Ophthalmol Strabismus. 2022;59(X):e32-e34.] .

Details

Language :
English
ISSN :
1938-2405
Volume :
59
Issue :
3
Database :
MEDLINE
Journal :
Journal of pediatric ophthalmology and strabismus
Publication Type :
Academic Journal
Accession number :
35603949
Full Text :
https://doi.org/10.3928/01913913-20220420-01