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. If not treated, the tumors will continue growing. The cancer may grow along the optic nerve and reach the brain or it may travel to other parts of the body.
Cancer occurs when cells in the body (in this case retina cells) divide without control or order. Normally, cells divide in a regulated manner. If cells keep dividing uncontrollably when new cells are not needed, a mass of tissue forms, called a growth or tumor. Tumors can invade nearby tissue and spread to other parts of the body.
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. Some cases of the tumor are inherited; others are not.
A risk factor is something that increases your chance of getting a disease or condition.
It typically happens in children less than 5 years old.
Risk factors for retinoblastoma include:
- Defect in retinoblastoma gene
- 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
The doctor will ask about symptoms and family medical history, and perform a physical exam. Many retinoblastomas are found during routine physical exams. If a tumor is suspected, the 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 a day or two of birth. Additional eye exams are scheduled at regular intervals thereafter.
Once retinoblastoma is found, staging tests are performed. The clinical stage it based on
- Tumor size, appearance, and amount of invasion into surrounding areas
- Location of the tumor inside the eye
- Amount of retinal detachment
- Spread of tumor outside the eye
Treatment depends on the stage of the cancer. The cancer may be localized to the eyes or it may have spread to tissues around the eye or to other parts of the body.
Tests may include, but are not limited to:
- Dilated eye exam—The pupil is dilated with eye drops. Then, the inside of the eye is examined with a lighted instrument that allows the examiner to view structures inside the eye.
- Ultrasound—to examine the inner part of the eye.
- MRI scan —to check for spread of the cancer to the brain or other tissue.
- CT scan —may be done to check if the cancer has spread to other areas.
General anesthesia may be given to keep the child still during close examination and testing.
Your child will likely be referred to a specialist for treatment. Without treatment, the cancer cells will continue to grow.
Treatment aims to cure the cancer and preserve sight. Options vary, depending on the stage. Therapies may be used alone or in combination.
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 therapy—radiation directed at the tumor from a source outside the body
- Internal radiation therapy—radioactive materials placed into the body near the cancer cells
Used on small tumors, cryotherapy is the use of cold to freeze and destroy cancer cells.
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.
Genetic counseling and close monitoring and screening for people at risk for retinoblastoma can help prevent the disease or detect it early if it occurs.
Early diagnosis and treatment improve the chance of successful treatment. 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.
- Monitoring for recurrence—People who have been treated for retinoblastoma require regular medical exams to assess the success of treatment and check for recurrence or bilateral disease.
- Monitoring for other cancers—Children with retinoblastoma are at increased risk for an associated brain tumor and other cancers in the body.
- Reviewer: Eric L. Berman, MD
- Update Date: 09/01/2011 -