Retinoblastoma can be treated upon early detection

“Several cancers are treatable, however, there still remains lack of awareness about this fact”

New Delhi 3rd February 2018:

A rare form of cancer, affecting only about 2,000 people in India per year, Retinoblastoma, is the most common among the cancers of the eye in children under the age of five. About 92% of such children live in the developing nations. Many children lose their eye sight or die from this cancer due to lack of awareness of the initial signs of presentation, poor access to proper treatment or lack of finances to finish the treatment.

Retinoblastoma is a cancer that starts in the retina, the very back part of the eye. It occurs when nerve cells in the retina develop genetic mutations. These mutations cause the cells to continue growing and multiplying when healthy cells would die. This accumulating mass of cells forms a tumor.

Speaking about this, Padma Shri Awardee Dr K K Aggarwal, President Heart Care Foundation of India (HCFI) and Immediate Past National President Indian Medical Association (IMA), said, “In children with retinoblastoma, the disease often affects only one eye. However, one out of three children with retinoblastoma develops cancer in both eyes. One of the first common signs of this cancer is a visible whiteness in the pupil called ‘cat’s eye reflex’ or leukocoria. This becomes more noticeable in dim light or in photographs taken with a flash. On World Cancer Day, it is important to raise awareness on the fact that Retinoblastoma is often curable when it is diagnosed early. However, if it is not treated promptly, this cancer can spread beyond the eye to other parts of the body. This advanced form of retinoblastoma can be life-threatening.”


Some other symptoms of this condition include poorly aligned or “wandering” eye, known as strabismus; reddish pupil, often with pain; larger-than-normal pupil; different-colored irises; and poor vision or decreased vision.

Adding further, Dr Aggarwal, who is also the Group Editor of IJCP, said, “When retinoblastoma is suspected, a pediatric ophthalmologist examines the retina by dilating the eye, sometimes under general anesthesia. They may also prescribe some imaging tests, like an ultrasound of the eye, a computerized tomography (CT) scan, or magnetic resonance imaging (MRI), as well as blood tests.”

People with retinoblastoma may want to consider genetic counseling before having children to learn more about the risks of passing on the gene change and perhaps to explore ways to avoid this. If a preventive option is not used, children born to a parent with a history of retinoblastoma should be screened for this cancer starting shortly after birth because early detection of this cancer greatly improves the chance for successful treatment.

One of the focus of the year ling 25th years of Perfect Health Mela Celebrations will be on retinoblastoma awareness.

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