Retinoblastoma is a rare type of eye cancer that affects children younger than five.
Retinoblastoma is a rare type of eye cancer that affects children younger than five.
Babies with a family history of retinoblastoma will be screened for the cancer soon after birth.
The following information is for parents or carers of children who have just been diagnosed with retinoblastoma. It explains:
Retinoblastoma is cancer of the retina. The retina is the light-sensitive lining at the back of the eye. Retinoblastoma causes the cells of the retina to grow rapidly and out of control. One or both eyes may be affected by the cancer.
In about 40% of cases, retinoblastoma is caused by a faulty gene. This may be inherited from the child's parents or may develop randomly when the child is developing in the womb.
To check for retinoblastoma, an eye specialist will examine the child's eyes by shining a light into them. If retinoblastoma is diagnosed or if there is a family history of retinoblastoma, the child will be checked by screening every few months for five years.
If retinoblastoma has affected both eyes, it is usually diagnosed in the first year of life. If only one eye is affected, it may not be diagnosed until the child is around 18–30 months old.
Most cases of retinoblastoma are found early and are successfully treated before the cancer spreads outside the eyeball. When the cancer is entirely within the eye, it is known as intraocular retinoblastoma.
The Childhood Eye Cancer Trust website has information about all the treatments for retinoblastoma mentioned below, including their side effects.
Treating a small tumour that is completely inside the eye usually involves one of the following treatments:
Larger tumours will be treated with one or a combination of the following treatments:
**Radioactive plaque – if the tumour is not too large, a small radioactive disc is stitched over the cancerous cells and left in place for a few days to destroy the tumour, before the disc is removed.
If the cancer has spread beyond the eye (extraocular retinoblastoma), it has the potential to spread around the body and is more difficult to treat.
It's important to be aware of the warning signs of retinoblastoma. Two common signs are:
Sometimes, the iris (the coloured part of the eye) may change colour, or the child may complain that they cannot see as well as they used to.
These signs may be due to something other than retinoblastoma, but you should still get them checked by a doctor immediately. The doctor should carry out a red reflex assessment (PDF, 314Kb).
It is unusual for retinoblastoma to progress unnoticed until the child is older than five. In these rare cases, the eye may be red, sore or swollen, and there may be loss of vision.
The Childhood Eye Cancer Trust (CHECT) website provides information about retinoblastoma. It also offers help and support to parents and carers of affected children as well as adults who were affected as a child. CHECT can also put you in touch with other parents of affected children.
Important: Our website provides useful information but is not a substitute for medical advice. You should always seek the advice of your doctor when making decisions about your health.