Return to Index
Retinoblastoma is a rare type of cancer found in the eye. In retinoblastoma, one or more tumors form in the retina. The retina is a layer of light-sensitive tissue that lines the back of the eye. It converts visual images into nerve impulses in the brain that allow us to see.
As with most cancers, early diagnosis and treatment lead to better outcomes.
|Retina of the Eye|
|Copyright © Nucleus Medical Media, Inc.|
During early stages of fetal development, fast-growing, immature cells called retinoblasts form. Later, these cells become retinal cells. In retinoblastoma, some of these cells quickly grow out of control. If cells keep dividing uncontrollably when new cells are not needed, a mass of tissue called a tumor grows. The cancer may grow along the optic nerve and reach the brain, or it may travel to other parts of the body.
Retinoblastoma is caused by defects in the retinoblastoma gene.
Retinoblastoma is more common in children under 5 years old. Other factors that may increase your child's chance of retinoblastoma are family members with retinoblastoma.
Retinoblastoma usually forms only in one eye, but both eyes may have tumors. Symptoms are usually noticed by the parent or caregiver and may include, but are not limited to:
- Eyes do not look normal, often described as a glazed look or a “cat’s eye.”
- When a light is directed at the eye, the pupil looks white rather than red. This is often noticed on a photograph.
- Eyes may appear to be crossed or looking in different directions.
Less common symptoms may include:
- Eye may grow in size
- Eye pain
- Redness in the white part of the eye
- Excessive tearing
- Pupil may not respond to light
- Iris (colored part of the eye) changes color
- Double vision
|Normal Anatomy of the Eye|
|Copyright © Nucleus Medical Media, Inc.|
You will be asked about your symptoms and family medical history. A physical exam will be done. Many retinoblastomas are found during routine physical exams. If a tumor is suspected, your child will usually be referred to a specialist for a more complete eye exam. In children with a family history of the disease, eye exams often begin within 1-2 days of birth. Additional eye exams are scheduled at regular intervals thereafter.
Tests may include:
- Dilated eye exam—To examine the inside of the eye with a lighted instrument.
- Imaging test to evaluate the eye and surrounding tissue may include:
Microscopic evaluation of the tumor
- Routine biopsy is not usually done
- Biopsies from surrounding area or bone marrow will be done if the tumor might have spread
- Spinal fluid is examined if spread to the central nervous system is suspected
The physical exam combined with all of the test results, will help to determine the stage of cancer. Staging is used to guide your child's treatment plan. Like other cancers, retinoblastoma is staged from I-IV. Stage I is a very localized cancer, while stage IV indicates a spread to other parts of the body.
Treatment depends on the stage of the cancer. Treatment aims to cure the cancer and preserve sight.
Therapies may be used alone or in combination, and may include:
This involves surgical removal of the entire eye and as much of the optic nerve as possible. The optic nerve is the nerve leading from the eye to the brain that is responsible for vision. Surgery may be used for a large tumor in one eye.
This treatment involves the use of radiation to kill cancer cells and shrink tumors. Radiation may be:
- External—radiation directed at the tumor from a source outside the body
- Internal—radioactive materials placed into the body near the cancer cells
Cryotherapy is the use of cold to freeze and destroy small tumors.
This treatment uses heat to kill cancer cells.
Lasers are used to destroy a small tumor.
Chemotherapy is the use of drugs to kill cancer cells. This treatment may be given in many forms including pill, injection, and through a catheter. The drugs enter the bloodstream and travel through the body killing mostly cancer cells, but also some healthy cells.
Prevention and early detection techniques include:
- Screening—Children born into families with a history of retinoblastoma should have regular eye exams to screen for development of the tumor. All children should have regular eye screening by their doctor.
- Genetic counseling—This may help determine a person’s risk of developing retinoblastoma. If you have retinoblastoma or have a family history of the disorder, you can talk to a genetic counselor when deciding to have children.
American Cancer Society
National Cancer Institute
BC Cancer Agency
Canadian Cancer Society
Retinoblastoma. EBSCO DynaMed Plus website. Available at: http://www.dynamed.com/topics/dmp~AN~T115082/Retinoblastoma . Updated June 27, 2017. Accessed December 15, 2017.
Retinoblastoma. Merck Manual Professional Version website. Available at: http://www.merckmanuals.com/professional/pediatrics/pediatric-cancers/retinoblastoma. Updated August 2015. Accessed December 15, 2017.
What is retinoblastoma? Eye Smart—American Academy of Ophthalmology website. Available at: https://www.aao.org/eye-health/diseases/what-is-retinoblastoma. Updated September 1, 2017. Accessed December 15, 2017.
- Reviewer: EBSCO Medical Review Board Michael Woods, MD, FAAP
- Review Date: 11/2018
- Update Date: 12/20/2014