A Case of Retinal Dysplasia with PHPV.
- Author:
So Yeung KIM
1
;
Jong Moon PARK
Author Information
1. Department of Opthalmology, College of Medicine, Gyung Sang National University Chinju, Korea.
- Publication Type:Case Report
- Keywords:
Retinal dysplasia;
Retinoblastoma;
Rosette
- MeSH:
Gliosis;
Humans;
Infant;
Male;
Retina;
Retinal Dysplasia*;
Retinaldehyde*;
Retinoblastoma
- From:Journal of the Korean Ophthalmological Society
1995;36(5):885-889
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Retinal dysplasia is an abnormal differentiation of the retina at embryonal retina stage with proliferation of its elements into rosettes, fold, and gliosis and it is very difficulat to distinguish between the various types of intraocular disease, especilaly retinoblastoma. We experienced a case of unilateral retinal dysplasia without systemic abnormalities occurring in a 5 months old boy. It was clinically suspected Retinoblastoma, which was proved to be Retinal Dysplasia by histopathologic examination.
