Eye Cancer
Overview of EyeCancer
Eye cancer refers to the malignant tumors that arise or occur near the eye. The eyelids and tear glands ( adnexa), orbit ( the tissue that surrounds the eyeball), or eyeball( globe) can be involved. Survival and vision preservation are possible with early detection, and hence, early detection is highly encouraged.
Eye Cancer Types
Retinoblastoma
•A rare but aggressive form of cancer that originates in the retina, most frequently occurring in children younger than 5 years old. Symptoms can include a white reflex within the pupil or crossed eyes. Treatment is chemotherapy, laser treatment, cryotherapy, or even the removal of the eye in very advanced stages. Early diagnosis can salvage both vision and life.
Uveal Melanoma
•The most frequent primary intraocular cancer in adults that develops from the pigmented uveal tract (iris, ciliary body, or choroid). It usually develops symptomlessly but may lead to loss of vision, floaters, or flashes of vision. Treatment options may include radiation therapy (brachytherapy or proton beam therapy), laser treatment, or removal of the eye in extreme cases.
Ocular Surface Squamous Neoplasia (OSSN)
•A tumor of the conjunctiva or cornea, which commonly occurs in sun-exposed persons or immunocompromised patients. Presents as a white or pink swelling on the surface of the eye. Topical chemotherapy, surgical removal, or cryotherapy is used to treat it. Follow-up is crucial because there is a tendency to recur.
Sebaceous Gland Carcinoma
•A malignant and very rare tumor derived from oil glands in the eyelid. It can masquerade as a benign eyelid infection, leading to delayed diagnosis. It presents with a painless swelling of the eyelid, loss of eyelashes, or swelling of the eyelid. Surgery is the typical treatment and radiation may be added if the tumor is large.
Lymphoma of the Eye
•Usually involves the conjunctiva, orbit, or uvea and is related to systemic lymphoma. Symptoms include painless swelling, proptosis, or diplopia. It is diagnosed through biopsy. Radiation and chemotherapy are usually used based on the type and extent of disease.
Eye Cancer Symptoms
- •
Sudden blurriness, double vision, or partial loss of vision can be signs of a tumor compressing parts of the eye.
- •
A white sheen in the pupil (particularly in children) observed in photographs or low light may be an early indicator of retinoblastoma.
- •
A white or pink mass on the surface of the eye or eyelid can indicate ocular surface cancers such as OSSN or sebaceous gland carcinoma.
- •
Forward protrusion or puffiness of the eye can result from orbital lymphoma or metastatic eye malignancies.
- •
Chronic redness, pain, or grittiness might be associated with surface-based tumors or eyelid cancers.
- •
Thickening, discoloration, or lost lashes—particularly on one side—must be checked for possible eyelid tumors.
What’s Notable
The most common eye cancer in children is retinoblastoma, and the most common one in adults is melanoma.
Certain eye cancers are even detectable through a routine eye checkup before any symptoms are felt.
Exposure to UV radiation for many years, particularly without protective eye cover, increases the risk of ocular melanoma and surface eye cancers.
When to Seek Help
Key signs of an eye tumor include sudden vision changes, visible dark spots or bulging, persistent pain or redness, flashes or floaters, loss of side vision, and unexplained tearing or swelling. These symptoms should be promptly checked by an eye specialist.
Eye Cancer Causes & Risk Factors
Age and Heredity
Retinoblastoma occurs in early childhood, but melanoma and lymphoma of the eye occur in most older people. Gene mutations that are hereditary, such as RB1, are unsafe.
Sunlight and UV Exposure
Exposure to UV radiation for many years, particularly without protective eye cover, increases the risk of ocular melanoma and surface eye cancers.
Fair Skin and Light Eyecolor
Individuals with blue, green, or gray-colored eyes and light skin coloured are at increased risk for developing intraocular melanoma.
Family History of Eye Cancer
A first-degree relative with retinoblastoma, uveal melanoma, or other eye cancer suggests a genetic component and should prompt early evaluation.
Immune Suppression and HIV/AIDS
Those with compromised immunity are at increased risk for developing eye lymphomas or eye Kaposi sarcoma.
Exposure to Specific Chemicals
Occupational exposure to welding fumes, pesticides, or solvents may be associated with greater risks of eye cancer.
Eye Cancer Diagnosis
Symptom Awareness & Initial Check-up
Step 1: Symptom Awareness & Initial Check-up
Blurred vision, partial blindness, eye pain, or an increasing dark spot should lead to an immediate eye test by an ophthalmologist.
Complete Eye Examination
Step 2: Complete Eye Examination Your expert will inspect the inside of the eye with equipment such as ophthalmoscopy, slit-lamp examination, and ultrasound to identify abnormal masses.
Imaging & Diagnostic Scans
Step 3: Imaging & Diagnostic Scans
MRI or CT scans are employed to measure tumor size, site, and possible spread, particularly if cancer is suspected behind or around the eye.
Biopsy or Fine Needle Aspiration (FNA)
Step 4: Biopsy or Fine Needle Aspiration (FNA)
A small tissue sample of the tumor is removed when necessary to establish cancer type, particularly when imaging results are not conclusive.
Genetic & Molecular Testing
Step 5: Genetic & Molecular Testing
Genetic testing (e.g., BAP1 mutation, loss of chromosome 3) predicts tumor behavior and directs individualized treatment strategies.
Multidisciplinary Planning
Step 6: Multidisciplinary Planning
Multidisciplinary planning by an ocular oncology care team, including radiation oncologists and genetic counselors, produces a tailored treatment plan with an emphasis on preservation of the eye and survival.
Step 1: Symptom Awareness & Initial Check-up
Blurred vision, partial blindness, eye pain, or an increasing dark spot should lead to an immediate eye test by an ophthalmologist.
Step 2
Complete Eye Examination
Step 3
Imaging & Diagnostic Scans
Step 4
Biopsy or Fine Needle Aspiration (FNA)
Step 5
Genetic & Molecular Testing
Step 6
Multidisciplinary Planning
Recovery
Vision Monitoring
•Periodic eye checkup and screening for vision change and tumor control.
Post-Treatment Care
•Protection of eyes and lubricating drops after surgery or radiation, and healing ointments.
Rehabilitation Support
•Visual aids such as magnifying glasses or prosthetic eyes can help restore independence and enhance quality of life following loss of an eye or blindness.
Mental Health Counseling
•Presence of counselors or psychologists to handle fear of recurrence, depression, or anxiety.
Peer Support
•Reach out to other eye cancer or vision loss support group survivors who have survived eye cancer.
Stress Relief Techniques
•Journaling, telling your story, and creating art can be helpful in completing your experience.
Travel accommodations
•Re-training to travel safely with a change of vision.
Home adaptations
•Use of amplified lighting, high contrast color and touch cues to function independently.
Workplace accommodations
•Use of screen readers, large print, or altered responsibilities to adjust for any loss of vision.
Eye Cancer Types
Retinoblastoma
•A rare but aggressive form of cancer that originates in the retina, most frequently occurring in children younger than 5 years old. Symptoms can include a white reflex within the pupil or crossed eyes. Treatment is chemotherapy, laser treatment, cryotherapy, or even the removal of the eye in very advanced stages. Early diagnosis can salvage both vision and life.
Uveal Melanoma
•The most frequent primary intraocular cancer in adults that develops from the pigmented uveal tract (iris, ciliary body, or choroid). It usually develops symptomlessly but may lead to loss of vision, floaters, or flashes of vision. Treatment options may include radiation therapy (brachytherapy or proton beam therapy), laser treatment, or removal of the eye in extreme cases.
Ocular Surface Squamous Neoplasia (OSSN)
•A tumor of the conjunctiva or cornea, which commonly occurs in sun-exposed persons or immunocompromised patients. Presents as a white or pink swelling on the surface of the eye. Topical chemotherapy, surgical removal, or cryotherapy is used to treat it. Follow-up is crucial because there is a tendency to recur.
Sebaceous Gland Carcinoma
•A malignant and very rare tumor derived from oil glands in the eyelid. It can masquerade as a benign eyelid infection, leading to delayed diagnosis. It presents with a painless swelling of the eyelid, loss of eyelashes, or swelling of the eyelid. Surgery is the typical treatment and radiation may be added if the tumor is large.
Lymphoma of the Eye
•Usually involves the conjunctiva, orbit, or uvea and is related to systemic lymphoma. Symptoms include painless swelling, proptosis, or diplopia. It is diagnosed through biopsy. Radiation and chemotherapy are usually used based on the type and extent of disease.
Eye Cancer Symptoms
- •
Sudden blurriness, double vision, or partial loss of vision can be signs of a tumor compressing parts of the eye.
- •
A white sheen in the pupil (particularly in children) observed in photographs or low light may be an early indicator of retinoblastoma.
- •
A white or pink mass on the surface of the eye or eyelid can indicate ocular surface cancers such as OSSN or sebaceous gland carcinoma.
- •
Forward protrusion or puffiness of the eye can result from orbital lymphoma or metastatic eye malignancies.
- •
Chronic redness, pain, or grittiness might be associated with surface-based tumors or eyelid cancers.
- •
Thickening, discoloration, or lost lashes—particularly on one side—must be checked for possible eyelid tumors.
What’s Notable
The most common eye cancer in children is retinoblastoma, and the most common one in adults is melanoma.
Certain eye cancers are even detectable through a routine eye checkup before any symptoms are felt.
Exposure to UV radiation for many years, particularly without protective eye cover, increases the risk of ocular melanoma and surface eye cancers.
When to Seek Help
Key signs of an eye tumor include sudden vision changes, visible dark spots or bulging, persistent pain or redness, flashes or floaters, loss of side vision, and unexplained tearing or swelling. These symptoms should be promptly checked by an eye specialist.
Eye Cancer Causes & Risk Factors
Age and Heredity
Retinoblastoma occurs in early childhood, but melanoma and lymphoma of the eye occur in most older people. Gene mutations that are hereditary, such as RB1, are unsafe.
Sunlight and UV Exposure
Exposure to UV radiation for many years, particularly without protective eye cover, increases the risk of ocular melanoma and surface eye cancers.
Fair Skin and Light Eyecolor
Individuals with blue, green, or gray-colored eyes and light skin coloured are at increased risk for developing intraocular melanoma.
Family History of Eye Cancer
A first-degree relative with retinoblastoma, uveal melanoma, or other eye cancer suggests a genetic component and should prompt early evaluation.
Immune Suppression and HIV/AIDS
Those with compromised immunity are at increased risk for developing eye lymphomas or eye Kaposi sarcoma.
Exposure to Specific Chemicals
Occupational exposure to welding fumes, pesticides, or solvents may be associated with greater risks of eye cancer.
Eye Cancer Diagnosis
Symptom Awareness & Initial Check-up
Step 1: Symptom Awareness & Initial Check-up
Blurred vision, partial blindness, eye pain, or an increasing dark spot should lead to an immediate eye test by an ophthalmologist.
Complete Eye Examination
Step 2: Complete Eye Examination Your expert will inspect the inside of the eye with equipment such as ophthalmoscopy, slit-lamp examination, and ultrasound to identify abnormal masses.
Imaging & Diagnostic Scans
Step 3: Imaging & Diagnostic Scans
MRI or CT scans are employed to measure tumor size, site, and possible spread, particularly if cancer is suspected behind or around the eye.
Biopsy or Fine Needle Aspiration (FNA)
Step 4: Biopsy or Fine Needle Aspiration (FNA)
A small tissue sample of the tumor is removed when necessary to establish cancer type, particularly when imaging results are not conclusive.
Genetic & Molecular Testing
Step 5: Genetic & Molecular Testing
Genetic testing (e.g., BAP1 mutation, loss of chromosome 3) predicts tumor behavior and directs individualized treatment strategies.
Multidisciplinary Planning
Step 6: Multidisciplinary Planning
Multidisciplinary planning by an ocular oncology care team, including radiation oncologists and genetic counselors, produces a tailored treatment plan with an emphasis on preservation of the eye and survival.
Step 1: Symptom Awareness & Initial Check-up
Blurred vision, partial blindness, eye pain, or an increasing dark spot should lead to an immediate eye test by an ophthalmologist.
Step 2
Complete Eye Examination
Step 3
Imaging & Diagnostic Scans
Step 4
Biopsy or Fine Needle Aspiration (FNA)
Step 5
Genetic & Molecular Testing
Step 6
Multidisciplinary Planning
Recovery
Vision Monitoring
•Periodic eye checkup and screening for vision change and tumor control.
Post-Treatment Care
•Protection of eyes and lubricating drops after surgery or radiation, and healing ointments.
Rehabilitation Support
•Visual aids such as magnifying glasses or prosthetic eyes can help restore independence and enhance quality of life following loss of an eye or blindness.
Mental Health Counseling
•Presence of counselors or psychologists to handle fear of recurrence, depression, or anxiety.
Peer Support
•Reach out to other eye cancer or vision loss support group survivors who have survived eye cancer.
Stress Relief Techniques
•Journaling, telling your story, and creating art can be helpful in completing your experience.
Travel accommodations
•Re-training to travel safely with a change of vision.
Home adaptations
•Use of amplified lighting, high contrast color and touch cues to function independently.
Workplace accommodations
•Use of screen readers, large print, or altered responsibilities to adjust for any loss of vision.
At Everhope, our dedicated team supports your journey with advanced care, compassionate guidance, and lasting hope.
New ocular melanoma cases reported annually in US.
New retinoblastoma cases reported in India in 2022
live births in India develops retinoblastoma at birth.
FAQs on Eye Cancer
No question is too small when it comes to your care
Yes, the majority of eye cancers can be cured—especially if discovered at an early stage. The chance of cure depends on the type, size, and site of the tumor.
Not always. Sight is saved in certain treatments but not in others (e.g., enucleation or radiation). Vision rehabilitation will help you cope.
Eye cancer is detected by a thorough eye examination, imaging tests (like ultrasound or MRI), and sometimes by biopsy.
No, it is uncommon. Children get retinoblastoma, and ocular melanoma happens more in adults.
Some types, like retinoblastoma, are associated with a gene. Genetic counseling is normally recommended to those at risk.
Yes, especially the more aggressive forms like ocular melanoma, which can spread to the liver or lungs. Early treatment reduces this risk.
Blurred vision, floaters, dark spots, flashes of light, or growth visible within the eye—see a doctor if you observe these.
Yes, regular checkups are needed to monitor for recurrence, vision changes, or complications of treatment.
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EBD 65, Sector 65, Golf Course Extension Road, Gurgaon