

Eye cancer in children, also known as retinoblastoma, is a rare but very serious condition if not detected early. A child with this condition may show subtle signs that parents can easily overlook, such as a white reflection in the pupil, vision problems, or eye misalignment (strabismus).Early detection of retinoblastoma plays a major role in successful treatment and in preserving the child’s vision.In this Dalily Medical article, we will discuss the symptoms of eye cancer in children, methods of early detection, and the most important steps for prevention and treatment, explained in a simple and clear way for every parent.
Eye cancer in children is most commonly retinoblastoma, a tumor that develops in the retina and affects the child’s ability to see.
In some cases, retinoblastoma can be hereditary. That’s why genetic screening for newborns with a family history is important for early detection.
Yes, follow-up is essential to monitor:
Eye growth
Visual function
Early detection of recurrence
It depends on the tumor’s size, location, and time of diagnosis.
In early stages, vision can often be preserved or significantly improved.
If a white or gray pupil appears
If the child suddenly develops strabismus (eye misalignment)
If there are signs of vision loss or abnormal eye movements
No, it is relatively rare, affecting about 1 in every 15,000–20,000 children worldwide.
Yes, hereditary cases can affect one or both eyes.
Complete prevention is not possible, but early detection, especially in children with a family history, improves treatment outcomes.
Most retinoblastomas are malignant, but with early treatment, it can be controlled and prevented from spreading.
Treatment duration depends on the tumor’s size and spread. It may range from a few sessions to several months in advanced cases.
Not always. Small tumors can sometimes be treated with:
Localized chemotherapy
Cryotherapy (freezing therapy)
Laser photocoagulation
Large tumors often require surgical intervention.
Most procedures are performed under general anesthesia, so the child does not feel pain during treatment. Post-operative discomfort can be managed with medication.
Yes, which is why regular follow-ups are crucial for early detection of recurrence.
Often yes. Children may need glasses, contact lenses, or vision therapy exercises to improve focus and clarity.
Yes, some treatments may affect eye growth or vision development. Careful, ongoing monitoring helps reduce long-term complications.
Retinoblastoma
Most common in children.
Origin: retina (light-sensitive layer).
Symptoms: white pupil (leukocoria), strabismus, vision loss.
Uveal Melanoma (very rare)
Origin: middle layer of the eye (uvea).
Symptoms: eye color changes, blurred vision, eye pain.
Vascular Tumors (e.g., Retinal Hemangioblastoma)
Benign tumors in retina or cornea.
Symptoms: abnormal blood vessels, eye redness, partial vision loss.
Lacrimal Gland Tumors (rare)
Appears as swelling above the eye.
Symptoms: eye bulging, mild pain, shape changes.
Iris or Choroidal Melanoma (rare)
Symptoms: iris color changes, strabismus, partial vision loss.
Other Embryonal Tumors (e.g., Medulloepithelioma)
Usually before age 5.
Symptoms: eye swelling, strabismus, redness, occasional pain.
Early Stage
Small, localized tumor in the retina.
Symptoms: occasional white pupil in photos, mild vision loss.
Localized Advanced Stage
Tumor grows and presses surrounding tissues.
Symptoms: clear strabismus, mild swelling/redness, poor vision.
Advanced Intraocular Stage
Tumor fills most of the eye.
Symptoms: significant vision loss, constant white pupil, eye pain.
Urgent medical intervention is required.
Extraocular Spread
Tumor extends beyond the eye to the lacrimal gland or nerves.
Symptoms: severe swelling, constant pain, complete vision loss.
Treatment: surgery, chemotherapy, or radiation to save the child’s life.
Vision loss (partial or complete)
Strabismus due to reduced vision in one eye
Intraocular spread (tumor filling the eye)
Extraocular spread (to nerves, glands, or brain)
Visual development problems (poor eye coordination)
Treatment complications (infection, glaucoma, structural changes)
Psychological impact (low self-esteem, social challenges)
Clinical Eye Exam
Checking for white/gray pupil, strabismus, or light sensitivity.
Exam with magnifying lens or ophthalmoscope.
Examination Under Anesthesia (EUA)
For infants and small children.
Allows detailed assessment of retina and optic nerve.
Imaging Tests
CT Scan: measures tumor size and spread.
MRI: evaluates tumor extension inside/outside the eye.
Fluorescein Angiography: highlights abnormal blood vessels.
Ocular Ultrasound
Safe, painless, measures tumor size and density.
Genetic or Blood Tests
For children with family history.
Detects genetic mutations linked to retinoblastoma.
Biopsy (in rare cases)
Usually avoided in retinoblastoma to prevent tumor spread.
Considered only after thorough medical evaluation.
Seek medical care early if you notice white pupil, strabismus, or vision problems.
Commit to regular follow-ups to track tumor response to treatment.
Stick to the treatment plan (surgery, chemo, or radiation) as prescribed.
Support the child emotionally to reduce the psychological impact of treatment and vision problems.
Emotional impact: Tumors and treatments can cause fear or anxiety.
Communication: Explain the condition simply and encourage the child to express their feelings.
Daily activities: Play and routine activities help the child adapt better.
Avoid trauma or accidental injury.
Use protective glasses if recommended by the doctor.
Healthy nutrition supports the immune system.
Ensure regular sleep patterns and age-appropriate physical activity.
Wash hands before touching the eyes or after play.
Gently clean the face and eyes to reduce irritation or infection risk.
Ask about any changes in tumor size or new symptoms.
Always consult the medical team about treatment concerns or side effects.
Description: Strong medicines used to destroy cancer cells.
Methods of administration:
Intravenous (IV)
Direct injection into the eye’s artery (Intra-arterial)
Injection into the vitreous cavity (Intravitreal)
Goals: Shrink the tumor before surgery or radiation, prevent spread, and preserve the eye and vision.
Medications that specifically attack tumor cells without major harm to the rest of the body.
Used based on the tumor’s genetic profile.
Anti-nausea drugs to ease chemotherapy side effects.
Medications to stimulate blood cell production.
Antibiotics or antifungals to prevent infections when immunity is weak.
Description: Removing the entire eye when it cannot be saved or when the tumor is very large.
After surgery: A prosthetic eye can be implanted for cosmetic purposes, with close follow-up to prevent recurrence.
Removing only the tumor while preserving as much of the eye as possible.
Best for: Small or localized tumors.
Advantage: Partial vision preservation, less cosmetic impact.
Using laser or freezing techniques to destroy tumor cells before or after partial resection.
Goal: Reduce tumor size and prevent local spread.
If the tumor is close to the lens or cornea, part of it may be removed.
Vision can be restored with artificial lenses or prescription glasses.
Treatment | Description | Method | When Used | Advantages | Possible Complications |
---|---|---|---|---|---|
Chemotherapy | Anti-cancer drugs to kill or shrink tumor cells | IV, intra-arterial, intravitreal | Multiple or large tumors, pre-surgery shrinkage | May control tumor without eye removal | Hair loss, fatigue, low white cells, vomiting, temporary liver/kidney impact |
Radiotherapy | High-energy radiation to destroy cancer cells | External beam or brachytherapy (plaque) | Tumors resistant to chemo, or after surgery if cells remain | Preserves healthy tissue, reduces tumor size | Eye inflammation, slowed eye growth, rare vision impact |
Cryotherapy | Freezing tumor cells with very low temperatures | Cold probe applied repeatedly to tumor | Small/medium tumors, especially at retinal edge | High precision, eye preservation, minimally invasive, repeatable | Temporary irritation, minor bleeding, temporary vision effects |
Photocoagulation (Laser Therapy) | Laser heats and destroys tumor or its blood supply | Focused laser beam under anesthesia | Small/medium tumors on retinal surface, often with chemo | High accuracy, eye preservation, minimally invasive, repeatable | Partial vision loss in treated area, temporary redness, mild scarring risk |
Even with the best surgeons and technology, sometimes surgery does not fully remove the tumor or preserve vision. Causes include:
Tumor size or location: Large tumors or those close to the optic nerve are harder to control.
Late diagnosis: Early detection greatly improves outcomes; advanced tumors have higher failure rates.
Poor response to chemo or radiation: Some tumors do not shrink enough for effective removal.
Surgical complications: Severe bleeding, infection, or eye damage may affect success.
Recurrence (Relapse): Tumor may return if cancer cells remain.
Persistent white pupil or eye color changes
Continued vision loss after recovery
Tumor growth or spread
Detailed evaluation by an eye cancer specialist
Retreatment options: second surgery, chemotherapy, radiation, laser, or cryotherapy
Strict follow-up for early detection of recurrence
Psychological support for the child and family to manage fear and stress