Eye neoplasm

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Eye neoplasm refers to any abnormal growth in the eye that can be either benign (non-cancerous) or malignant (cancerous). These growths can originate from any part of the eye or its surrounding structures, including the eyelid, orbit (eye socket), and intraocular (within the eye) regions such as the retina, choroid, and iris. Eye neoplasms can affect vision, and in some cases, they can be life-threatening if they are malignant and not treated promptly.

Types of Eye Neoplasms[edit | edit source]

Eye neoplasms can be classified based on their location and nature. Some of the common types include:

  • Uveal melanoma: The most common primary intraocular malignancy in adults, originating from melanocytes in the uvea, which includes the iris, ciliary body, and choroid.
  • Retinoblastoma: A malignant tumor primarily affecting children, originating from the retina. It can be hereditary or non-hereditary.
  • Conjunctival neoplasms: These include both benign (e.g., conjunctival nevus) and malignant (e.g., squamous cell carcinoma) growths on the conjunctiva, the clear membrane covering the white part of the eye and the inner eyelids.
  • Orbital tumors: Tumors occurring in the orbit, the bony cavity that contains the eye. These can be primary or secondary (metastatic) and can affect both adults and children.
  • Eyelid tumors: Including both benign (e.g., basal cell carcinoma, which is actually the most common eyelid tumor but is malignant) and malignant growths that affect the eyelids.

Symptoms[edit | edit source]

Symptoms of eye neoplasms vary depending on the type and location of the tumor. Common symptoms may include:

  • Visual disturbances (e.g., blurred vision, vision loss)
  • Visible mass on the eye or eyelid
  • Change in the appearance of the eye or eyelid (e.g., change in color, shape)
  • Pain or discomfort in or around the eye
  • Bulging of one eye
  • Double vision

Diagnosis[edit | edit source]

Diagnosis of eye neoplasms involves a comprehensive eye examination, which may include:

  • Visual acuity test: To assess how well the patient can see.
  • Fundus examination: To examine the back of the eye, including the retina and optic nerve.
  • Ultrasound: High-frequency sound waves are used to create images of the eye's interior.
  • Imaging tests such as MRI or CT scan may be used to determine the extent of the tumor and if it has spread.

Treatment[edit | edit source]

Treatment options for eye neoplasms depend on the type, size, and location of the tumor, as well as the patient's overall health. Options may include:

  • Surgery: To remove the tumor, sometimes requiring removal of the eye (enucleation) in cases of large malignant tumors.
  • Radiation therapy: High-energy rays are used to kill cancer cells.
  • Laser therapy: High-intensity light to destroy tumors, especially useful in certain cases of retinoblastoma and small intraocular tumors.
  • Chemotherapy: The use of drugs to kill cancer cells, often used for retinoblastoma.

Prognosis[edit | edit source]

The prognosis for patients with eye neoplasms varies widely depending on the type of tumor, its location, size, and whether it has spread. Early detection and treatment are crucial for improving outcomes.

Prevention[edit | edit source]

While there is no sure way to prevent eye neoplasms, regular eye examinations can help in early detection and treatment, potentially saving vision and life.

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