Related Experiment Video
Updated: May 12, 2026

07:55
Establishment and Propagation of Human Retinoblastoma Tumors in Immune Deficient Mice
Published on: August 4, 2011
Distant metastatic retinoblastoma without central nervous system involvement
Mohammad Javed Ali1, Santosh G Honavar, Vijay Anand Reddy
1Ocular Oncology Service, L. V. Prasad Eye Institute, Road No. 2, Banjara Hills, Hyderabad, India.
Indian Journal of Ophthalmology
|April 4, 2013
Summary
Retinoblastoma, a common childhood eye cancer, can metastasize, particularly in developing nations. This case highlights extensive bone metastasis from an initial orbital tumor, emphasizing diagnostic challenges.
Area of Science:
- Pediatric Oncology
- Ophthalmology
- Medical Imaging
Background:
- Retinoblastoma is the most frequent intraocular malignancy in children.
- Metastatic retinoblastoma is rare in developed countries but more common in developing nations.
- High mortality rates in developing countries are linked to late diagnosis and socio-economic factors.
Observation:
- This case report details an extensive skeletal metastasis.
- The metastasis originated from a massive orbital retinoblastoma.
- The initial presentation was a large orbital tumor.
Findings:
- Metastatic retinoblastoma presents a significant challenge in pediatric oncology.
- Late presentation and delayed diagnosis contribute to poor outcomes.
- The case illustrates the potential for extensive bone involvement.
Implications:
- Early detection and management of retinoblastoma are crucial, especially in resource-limited settings.
- Improved diagnostic strategies are needed to identify metastasis earlier.
- Further research into the management of metastatic retinoblastoma is warranted.
More Related Videos
Related Concept Videos
The Retinoblastoma Gene
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The Retinoblastoma Gene
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
