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WEBRetinoblastoma is a rare eye cancer that affects young children. Learn about the signs, risk factors, complications and treatments of this disease from Mayo Clinic experts.
WEBRetinoblastoma is a rare eye cancer that affects children. It can be heritable or sporadic, and it starts in the retina, the light-sensing layer of the eye. Learn how it develops, how it is diagnosed, and how it can spread to other parts of the body.
WEBRetinoblastoma is a rare childhood eye cancer that affects the retina. Learn about the symptoms, causes, diagnosis and treatment options for this condition, and how it can be inherited or sporadic.
WEBRetinoblastoma is a rare eye cancer that forms in the retina and can affect 1 or both eyes. Learn about the signs, risk factors, tests, and treatments for this condition from the National Eye Institute.
- Content medically reviewed by
Dr. Sanyukta Joshi
M.S., DNB, OphthalmologyView full profile on
LinkedInAn eye cancer that begins in the back of the eye (retina). It causes red eye and eye swelling. Commonly occurs in young children, but can rarely occur among adults.
Can be dangerous or life threatening if untreated
Rare (Fewer than 200,000 cases per year in US)
Treatable by a medical professional
Often requires lab test or imaging
Can last several months or years
Common for ages 5 and younger
Family history may increase likelihoodSource: Focus Medica . For informational purposes only. Consult a medical professional for advice. Learn more
Interesting reads - Retinoblastoma
Powered by Microsoft StartWEBRetinoblastoma (Rb) is a rare form of cancer that rapidly develops from the immature cells of a retina, the light-detecting tissue of the eye. It is the most common primary malignant intraocular cancer in children, and it is almost exclusively found in young children.
WEBRetinoblastoma is an intraocular malignancy with primitive neuroendocrine origins that primarily affects young children. ICD10 C69.2; ICD9 190.5; Incidence. Retinoblastoma is the most common intraocular malignancy afflicting children. The estimated incidence varies by country from 3.4 to 42.6 cases per million live births.
WEBRetinoblastoma is the most commonly encountered primary intraocular tumor of childhood and accounts for 3% of all childhood tumors. It is also the second most common intraocular malignant tumor. The number of retinoblastoma cases ranges from 1 in 14000 to 1 in 20000 live births. [6]
WEBRetinoblastoma is a rare eye cancer that affects young children. Learn about the signs, diagnosis and options for this disease from the American Academy of Ophthalmology.
WEBRetinoblastoma is a type of eye cancer that affects children, usually younger than 4 years old. Learn about the symptoms, diagnosis, staging and treatment options for this disease, which can be cured if detected early.
WEBCommon retinoblastoma treatments include chemotherapy, cold therapy and laser therapy. Radiation therapy may be another option. Surgery to remove the eye can treat retinoblastoma, but it's only used in certain situations.
Retinoblastoma—Patient Version - NCI - National Cancer Institute
WEBLearn about retinoblastoma, a rare childhood cancer of the retina, and its treatment options. Find out how to cope with cancer and access support resources.
Retinoblastoma Treatment - NCI - National Cancer Institute
WEBLearn about retinoblastoma, a rare eye cancer that affects children, and its treatment options. Find out how to diagnose, stage, and treat retinoblastoma, and what factors affect prognosis.
Retinoblastoma: Symptoms, Causes, Treatment, Outlook
WEBRetinoblastoma is a rare eye cancer that affects children under 5. It occurs when retinal cells have genetic mutations that make them grow out of control. Learn about the types, symptoms, treatment options, and survival rates of retinoblastoma.
What is retinoblastoma? - Cancer Research UK
WEBRetinoblastoma is a type of eye cancer that affects the retina, the light-sensitive layer at the back of the eye. It usually occurs in children under 5 and can be inherited or non-inherited. Learn about the causes, symptoms, diagnosis and treatment of retinoblastoma.
Retinoblastoma - NHS
WEBWhat is retinoblastoma? Symptoms. Causes. Tests and next steps. Treatment. Help and support. Find out about retinoblastoma, a rare type of eye cancer that can affect young children.
Retinoblastoma - St. Jude Children’s Research Hospital
WEBWhat is retinoblastoma? Retinoblastoma is a rare cancer of the retina, the thin membrane on the inside back of the eye that is stimulated by light. Retinoblastoma is usually diagnosed before a child reaches the age of 3. Retinoblastoma can be hereditary (passed down in families) or non-hereditary.
Retinoblastoma - GeneReviews® - NCBI Bookshelf
WEBRetinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma may be unifocal or multifocal.
Retinoblastoma Types, Symptoms, Treatment, and Prognosis
WEBRetinoblastoma is a type of eye cancer that affects the retina and occurs in about 1 in 18,000 births. Learn about the types, symptoms, causes, diagnosis, treatment, and prognosis of this rare condition.
Retinoblastoma: MedlinePlus Genetics
WEBRetinoblastoma is a rare type of eye cancer that usually develops in early childhood, often affecting only one eye. It can be hereditary or sporadic, and it can be cured if diagnosed early. Learn about the symptoms, causes, inheritance, and …
Treatment for Retinoblastoma | National Eye Institute
WEBLearn about the different treatments for retinoblastoma, a rare eye cancer that forms in the retina. Find out how chemotherapy, cryotherapy, laser therapy, radiation and surgery can help prevent vision loss and stop the cancer from spreading.
Modern treatment of retinoblastoma: A 2020 review - PMC
WEBRetinoblastoma, the most common ocular malignancy in childhood, is lethal if left untreated. In high-income countries (HICs), retinoblastoma is considered a curable cancer with a near 100% disease-free survival rate.
Retinoblastoma | Radiology Reference Article | Radiopaedia.org
WEBRetinoblastomas are the most common intraocular neoplasm found in childhood and with modern treatment modalities, are, in most cases, curable. On imaging, they are generally characterized by a heterogeneous retinal mass with calcifications, necrotic components and increased vascularization on Doppler ultrasound/enhancement on CT/MRI. Epidemiology.
Retinoblastoma: Etiology, Modeling, and Treatment - PMC
WEBRetinoblastoma is a retinal cancer that is initiated in response to biallelic loss of RB1 in almost all cases, together with other genetic/epigenetic changes culminating in the development of cancer.
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