ورم جذيعات الشبكية (Retinoblastoma)

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Retinoblastoma

 

(Diseases)

On this page, you will find everything you need to know about retinoblastoma.

What is retinoblastoma?

Retinoblastoma is a rare type of cancer characterized by the abnormal growth of cells in the retina of the eye. It most commonly affects children under the age of 5 and can be treated successfully when diagnosed at an early stage.

Sudden onset of strabismus (crossed eyes).

Change in pupil size.

What causes retinoblastoma?

Retinoblastoma occurs due to abnormal cell growth in the retina of children, resulting from a hereditary genetic mutation. However, there is no clear cause that explains why this mutation occurs.

Ultrasound imaging.

  • Genetic testing to determine whetherSpinal Tapthe condition is hereditary.
  • In some cases, thedoctor may also request:

Spinal tap (lumbar puncture) to check if cancer cells have spread.

Bone marrow biopsy to determine whether cancer cells have spread.

Cryotherapy (freezing therapy).

Eye removal surgery (enucleation).

How can retinoblastoma be prevented?

There is no known way to prevent retinoblastoma. However, genetic testing is recommended for couples planning to have children if there is a family history of the disease. It is also advised to maintain regular eye examinations for children during routine medical visits.

  • What are thecomplications of retinoblastoma?
  • The most common complications include:

Loss of vision in the affected eye.

If the cause is hereditary, the child may be at risk of developing another type of cancer.

 

When should you see a doctor?

You should see a doctor if any of the symptoms mentioned above appear, or if you notice any unusual changes in your child’s eyes or vision.

Frequently Asked Questions (FAQs):

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