The first step in diagnosing an ependymoma in children is to collect cerebrospinal fluid (CSF) from the child's spinal column. A lumbar puncture is performed by inserting a needle between the bones of the spine and removing a sample of CSF. The doctors examine the CSF for tumor cells, and may look for elevated protein levels and glucose levels. If the amounts of these markers are elevated, the child may have a tumor.
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The primary symptoms of ependymoma are headache, nausea, and confusion. In children, symptoms may also include stiff neck or back. Most cases occur in children between the ages of three and five, but can also occur in younger infants. The symptoms of ependymomas in childhood can be quite similar to those of other medical conditions, including irritability and fever. However, in some children, the symptoms may be similar to those of a more common disease, such as an infection.
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If a child has any of these symptoms, it is important to get immediate medical care. Treatment for ependymoma in children is essential to avoid the possibility of a life-threatening complication. During the course of treatment, children may experience emotional or behavioral side effects. They may experience chronic headaches, trouble walking, or other problems. It is important to seek medical attention as soon as possible.
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If a child has an ependymoma in childhood, the first treatment is surgery. This involves removing the tumor as much as possible. If it is too large, it may be too late to remove. The tumor will then be removed and sent to a neuropathologist for further analysis. After the diagnosis, a pediatric neurosurgeon will plan treatment. If an ependymomoma has recurred, the tumor will return again.
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Early symptoms of ependymoma in childhood are similar to those for a diagnosis of other types of cancer in children. During the first few months of life, the child may have an increased head circumference and swollen fontanelle. In addition to these symptoms, he or she may have a history of traumatic brain injury, seizures, and difficulty controlling bowels.
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The main treatment for ependymoma in children is surgery. In some cases, chemotherapy is used, but it may not be enough to prevent the tumor from coming back. Patients with ependymoma should see a doctor for regular monitoring. They should undergo regular MRI scans and follow-up appointments for several months. In the meantime, the child should be evaluated for neurological symptoms.
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If your child has any of these symptoms, it's important to seek medical attention immediately. You may experience a stiff neck, pain in the back, or seizures. While ependymoma can develop at any age, it is more likely to occur in childhood. Some children with the disease are not able to walk properly. This could lead to permanent damage to the brain.
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Children with ependymoma are twice as likely to develop the disease in the posterior fossa of the brain. If the tumor is affecting the posterior fossa, it may cause increased intracranial pressure. This can cause increased pressure in the head. In addition to increasing head circumference and swelling of the fontanelle, young children may also be unable to walk properly.
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A family history of ependyma can affect a child's chance of developing the disease. While a high risk of developing the disease, it is not a life-threatening condition. While the symptoms of ependyma are usually harmless, the disease may recur and affect the patient's quality of life. For those children, it is important to seek medical attention as soon as possible.
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Because of the high risk of spreading the disease, it is important to seek medical attention immediately. Surgical removal of the tumor is the only option when a tumor is too large. In rare cases, a tumor may require radiation. For children with ependymoma, however, the cancer is not likely to spread to other parts of the body. It is highly likely to spread, but ependymoma is rarely fatal.
