Spontaneous regression of retinoblastoma – A Case Report

Spontaneously regressing retinoblastoma is a retinal lesion consisting of one or moregray, translucent retinal masses, calcified nodules and retinal pigment migration and clumping in adjacent areas. Female child of 7 years presenting with esotropia LE was referred from pediatric Ophthalmology depart...

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Bibliographic Details
Main Authors: M Padma, N Shivanand, K Vishwanath
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:MRIMS Journal of Health Sciences
Subjects:
Online Access:http://www.mrimsjournal.com/article.asp?issn=2321-7006;year=2015;volume=3;issue=3;spage=232;epage=234;aulast=Padma;type=0
Description
Summary:Spontaneously regressing retinoblastoma is a retinal lesion consisting of one or moregray, translucent retinal masses, calcified nodules and retinal pigment migration and clumping in adjacent areas. Female child of 7 years presenting with esotropia LE was referred from pediatric Ophthalmology department to Vitreo-Retinal clinic of Sarojini Devi Eye Hospital, Hyderabad for fundus evaluation. Vision in RE is 6/6. LE –Perception of light positive, PR inaccurate in all quadrants. RE anterior segment examination is unremarkable and in LE – relative afferent pupillary defect. On fundus examination, RE – Normal, LE – Large circumscribed excavated area temporal to optic disc noticed. Spontaneously regressed retinoblastoma carries the same genetic implication as an active retinoblastoma.
ISSN:2321-7006
2321-7294