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Retinoblastoma (pediatric eye cancer)

Description Retinoblastoma is a...


Description

Retinoblastoma is a rare cancer of the eye. It involves the light sensing membrane in the back of the eye called the retina. It is a cancer that is often hereditary and usually affects children before the age of five. It causes five percent of all childhood blindness but, with treatment, vision can often be spared. Children diagnosed with retinoblastoma have an increased risk of other forms of cancer later in life.

Symptoms

Symptoms may include a white-appearing pupil, crossed eyes, tearing, bulging eyes, eye redness and different sized pupils.

Tests

Common tests used for diagnosis and treatment

Workup:
A complete history and physical will be performed. A specific ophthalmologic exam and examination of the retina will be performed. Imaging tests such as an ultrasound, CT scan or MRI may be performed.

Tests:
CT Scan, Magnetic resonance imaging (MRI), Ultrasound

Specialists:
Pediatrics, Pediatric Hematology and Oncology, Pediatric Ophthalmology

Treatment

Treatment varies but may include radiation, chemotherapy, laser therapy, cryotherapy, surgery or a combination of treatments. 
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Mediref: Retinoblastoma (pediatric eye cancer)
Retinoblastoma (pediatric eye cancer)
Mediref
https://mediref.blogspot.com/2018/08/retinoblastoma-pediatric-eye-cancer.html
https://mediref.blogspot.com/
https://mediref.blogspot.com/
https://mediref.blogspot.com/2018/08/retinoblastoma-pediatric-eye-cancer.html
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