Overview

Eye cancer, also known as ocular cancer or intraocular cancer, refers to a group of rare malignancies that develop within the various structures of the eye. Although eye cancer is relatively uncommon, it can have significant implications for vision and overall health. The two main types of eye cancer are primary intraocular cancer, which originates within the eye, and secondary intraocular cancer, which spreads to the eye from other parts of the body.

Primary intraocular cancer typically originates from three main structures of the eye: the retina, the uvea, and the conjunctiva. Retinoblastoma, the most common eye cancer in children, arises from the retina. This cancer primarily affects infants and young children and can result in vision loss or even fatal outcomes if not diagnosed and treated promptly. Melanoma, the most common primary eye cancer in adults, usually originates from the uvea, which consists of the iris, ciliary body, and choroid. Conjunctival cancer, while rare, can also develop on the thin, clear membrane that covers the white part of the eye.

Secondary intraocular cancer, on the other hand, occurs when cancer cells from other parts of the body metastasize or spread to the eye. Breast cancer, lung cancer, and skin cancer are among the most common cancers that can spread to the eye.

Symptoms of eye cancer may vary depending on the type and location of the tumor. Some common signs and symptoms include:

  1. Vision changes or loss: Blurred vision, seeing flashes or floaters, or a sudden decrease in vision may occur.
  2. Eye pain or discomfort: Persistent pain, redness, or irritation in the eye can be a symptom of eye cancer.
  3. Changes in the appearance of the eye: Bulging of the eye, a change in the shape or color of the iris, or a visible mass or growth on the eye’s surface may indicate a tumor.
  4. Changes in the pupil: An irregularly shaped or dilated pupil may be a sign of eye cancer.
  5. Changes in the field of vision: Shadows, dark spots, or partial loss of peripheral vision can occur.

If eye cancer is suspected, a comprehensive eye examination by an ophthalmologist is crucial for diagnosis. This may involve dilating the pupil and using specialized instruments to examine the structures of the eye. Additional tests such as ultrasound, optical coherence tomography (OCT), fluorescein angiography, or a biopsy may be performed to confirm the diagnosis and determine the extent of the cancer.

The treatment of eye cancer depends on several factors, including the type, size, and location of the tumor, as well as the patient’s overall health. Treatment options may include:

  1. Surgery: The removal of the tumor or the affected part of the eye is a common approach. In some cases, an artificial eye may be implanted to maintain the appearance of the eye.
  2. Radiation therapy: High-energy X-rays or other radiation sources can be used to kill cancer cells or shrink tumors.
  3. Chemotherapy: The use of drugs to destroy cancer cells, which may be administered systemically or directly into the eye.
  4. Targeted therapy: This involves using drugs that specifically target certain molecules or genetic mutations present in cancer cells.
  5. Laser therapy or cryotherapy: These techniques utilize extreme temperatures or lasers to destroy or freeze cancer cells.

Regular follow-up visits are essential after treatment to monitor for recurrence or the development of new tumors. Additionally, supportive care, such as counseling and low vision rehabilitation, may be necessary to address the emotional and functional consequences of eye cancer.

While eye cancer can have serious implications, early detection and prompt treatment offer the best chances of successful outcomes. It is important for individuals to maintain regular eye examinations, especially if they notice any concerning symptoms, and to seek medical attention promptly if any changes in vision or eye health occur.

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