There are many Retinoblastoma symptoms that can help you know if your child has this rare form of cancer. The symptoms of this rare disease are often difficult to spot, but there are some tests and treatments that can help you figure out if your child has the disease. Here are some of them. These tests may not show the full extent of the disease, but they can help you plan your treatment.
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A doctor will first conduct a thorough physical examination and may order tests to determine whether the cancer has spread to other parts of the body. If it has spread beyond the eye, it may be diagnosed as extraocular cancer. This type of cancer has spread to tissues surrounding the eye. Treatment options will vary, depending on the stage and risk group of your child. Usually, chemotherapy is used to control retinoblastoma.
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If the tumors spread to other parts of the eye, the fluid flow within the eye can become blocked. The pressure in the eye may cause vision loss. Thankfully, most cases of retinoblastoma are caught in time and treated successfully. If it spreads, however, it can be difficult to treat. Symptoms may include pain, vomiting, and neurological impairment. As with any cancer, it's important to seek medical attention as soon as you notice any changes.
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A white pupil in the eye may be another symptom of Retinoblastoma. This white spot is caused by a tumor reflecting light. Pictures taken with a flash camera may reveal this condition. It is essential to consult with a doctor immediately if you notice any of these Retinoblastoma symptoms in your child. A white pupil, a discolored iris, and problems with eye alignment may be signs of retinoblastoma.
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One of the major risks of retinoblastoma is inherited. People with inherited retinoblastoma often have multiple tumors in both eyes, and the disease is passed down from parent to child. However, people with hereditary retinoblastoma have an increased risk of other cancers in other parts of their body, including osteosarcoma, lung cancer, and aggressive skin cancer.
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Another Retinoblastoma symptom that can cause severe eye problems is white pupil. This symptom is known as leukocoria, and it is the most common symptom of the disease. Other symptoms of the disease include increased eye pressure, blurred vision, and changes in pupil size and color. Further, if the condition affects your child's vision, it can also lead to inflammation in the eye, or uveitis (inflammation of the middle layer of the eye).
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Retinoblastoma is a rare eye cancer that starts in the retina. The retina is the part of the eye that receives light and sends pictures to the brain. Retinoblastoma typically develops before a child reaches age two. Retinoblastoma symptoms include a white pupil and "red eye".
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In the event that the tumor spreads outside of the eye, the treatment will focus on removing it. Patients will be offered a range of treatments, such as radiation therapy, chemotherapy, and photocoagulation. After treatment, the eye will be monitored closely to see if the cancer has spread. Retinoblastoma is a deadly disease that can affect your vision. You must contact a physician if you think you might have this disease.
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Retinoblastoma symptoms may be difficult to identify in infants. They may also include a white pupil when light shines in it. Other common symptoms of Retinoblastoma include eye pain and redness. Your child may also experience a cloudy or white pupil. Your child's pediatrician will examine your child's eyes and perform tests to determine if they have any of these symptoms.
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A specialist may perform a specialized eye exam to determine the exact cause of Retinoblastoma. This exam may be performed under general anesthesia to limit movement. The doctor will use specialized light and instruments to determine whether there's a mass in the eye. If the mass is present, a tumor will be found. Otherwise, it will be referred to a pediatric oncologist for diagnosis and treatment.
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Retinoblastoma is hereditary. It develops due to mutations in the RB1 gene, which is located on chromosome 13 at positions q14.1-q14.2. The RB1 protein functions as a tumor suppressor, preventing cells from growing too rapidly. The RB1 protein may also affect the development of another cancer, such as osteogenic sarcoma.
