Retinocytoma: A Case Series

Retinoblastoma is the most common ocular malignancy in children, considered fatal without treatment. Retinocytoma is a rare benign clinical entity of retinoblastoma that shows signs of tumor regression. The clinical presentation of retinocytoma usually includes a gray translucent mass, intralesional...

Descripción completa

Detalles Bibliográficos
Autores principales: Bubshait, Luluah, Alburayk, Khalid, Alabdulhadi, Halla, Emara, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Ophthalmology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475323/
https://www.ncbi.nlm.nih.gov/pubmed/37667715
http://dx.doi.org/10.7759/cureus.42958
_version_ 1785100701726146560
author Bubshait, Luluah
Alburayk, Khalid
Alabdulhadi, Halla
Emara, Khalid
author_facet Bubshait, Luluah
Alburayk, Khalid
Alabdulhadi, Halla
Emara, Khalid
author_sort Bubshait, Luluah
collection PubMed
description Retinoblastoma is the most common ocular malignancy in children, considered fatal without treatment. Retinocytoma is a rare benign clinical entity of retinoblastoma that shows signs of tumor regression. The clinical presentation of retinocytoma usually includes a gray translucent mass, intralesional calcification, and retinal pigment epithelial alteration, along with the presence of chorioretinal atrophy. We report two cases of retinocytoma in patients presenting with strabismus in the Eastern Province of Saudi Arabia.
format Online
Article
Text
id pubmed-10475323
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cureus
record_format MEDLINE/PubMed
spelling pubmed-104753232023-09-04 Retinocytoma: A Case Series Bubshait, Luluah Alburayk, Khalid Alabdulhadi, Halla Emara, Khalid Cureus Ophthalmology Retinoblastoma is the most common ocular malignancy in children, considered fatal without treatment. Retinocytoma is a rare benign clinical entity of retinoblastoma that shows signs of tumor regression. The clinical presentation of retinocytoma usually includes a gray translucent mass, intralesional calcification, and retinal pigment epithelial alteration, along with the presence of chorioretinal atrophy. We report two cases of retinocytoma in patients presenting with strabismus in the Eastern Province of Saudi Arabia. Cureus 2023-08-04 /pmc/articles/PMC10475323/ /pubmed/37667715 http://dx.doi.org/10.7759/cureus.42958 Text en Copyright © 2023, Bubshait et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Ophthalmology
Bubshait, Luluah
Alburayk, Khalid
Alabdulhadi, Halla
Emara, Khalid
Retinocytoma: A Case Series
title Retinocytoma: A Case Series
title_full Retinocytoma: A Case Series
title_fullStr Retinocytoma: A Case Series
title_full_unstemmed Retinocytoma: A Case Series
title_short Retinocytoma: A Case Series
title_sort retinocytoma: a case series
topic Ophthalmology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475323/
https://www.ncbi.nlm.nih.gov/pubmed/37667715
http://dx.doi.org/10.7759/cureus.42958
work_keys_str_mv AT bubshaitluluah retinocytomaacaseseries
AT alburaykkhalid retinocytomaacaseseries
AT alabdulhadihalla retinocytomaacaseseries
AT emarakhalid retinocytomaacaseseries

Ejemplares similares