The ependymoma in childhood symptoms are similar to those of other types of brain tumors. The primary treatment of ependymoma is surgery, but chemotherapy and radiation therapy may be prescribed in some cases. The neurological exam may involve evaluating the child's vision, hearing, balance, and coordination. The child may also have seizures and difficulty swallowing.
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In some cases, radiation therapy may be recommended after surgery to shrink or destroy aggressive tumors. The treatment helps neurosurgeons remove the tumour completely. The specialized techniques of radiotherapy ensure that the radiation reaches the tumor cells while sparing healthy tissue. Some specialized techniques include conformal radiation therapy, intensity-modulated radiation therapy, proton therapy, and stereotactic radiosurgery. These treatments aim to target the tumour with multiple beams of radiation to kill the diseased cells.
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The ependymoma in childhood symptoms vary. Although this cancer is common in adults, children are at a greater risk. The symptoms can differ depending on age, but they are similar to those of any other type of brain tumor. Generally, the cancer develops in the spine or the brain. Young infants may be irritable, have difficulty sleeping, or have irregular head growth. If you think your child may have a brain tumor, you should seek medical treatment immediately.
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A childhood ependymoma may occur in the brain and spinal cord. If your child has any symptoms related to this condition, it is important to seek diagnosis from a qualified medical practitioner. In addition to surgery, a biopsy may be necessary to confirm a diagnosis. If an ependymoma is detected early, it can be treated. When diagnosed early, however, treatment is critical to the child's well-being.
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While ependymoma in childhood can be treated with surgery, there are several other risks associated with the procedure. It is important to visit a pediatrician to determine whether your child is suffering from a brain tumour. Most children who have ependyma will be monitored for the first few months following the surgery. The doctor will be able to give you a proper diagnosis based on the symptoms and history you've experienced.
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Most children with an ependymoma will have a normal brain scan. If it is in the top part of the brain, the neurosurgeon will remove it without harming the healthy tissue surrounding the tumour. Patients who have ependymoma in childhood usually do not require additional treatment for the disease. The child will undergo regular MRI scans to monitor recurrence. They will be reviewed by a Neuro-Oncology Long Term Effects clinic to determine the patient's long-term growth and development needs.
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The symptoms of ependymoma in childhood are similar to those of other cancers in the same area of the brain. In children with an inherited family cancer syndrome, the symptoms of ependymomas are common. Depending on the type of ependymomoma in childhood, these symptoms can include headaches, seizures, and visual disturbances. A pediatrician will perform a lumbar puncture to detect any underlying conditions that affect the child.
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Most ependymoma in childhood will manifest with pain in the neck or back. The symptoms of ependymoma will vary from child to child. A child may experience a range of symptoms that include loss of balance, difficulty walking, and confusion. Often, the tumour will be diagnosed with a brain imaging test. Further tests may include blood work and MRIs of the spinal cord.
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A child with an ependymoma in childhood can display several symptoms. The symptom list includes nausea, confusion, pain, and swelling in the neck. Surgical removal of the ependyma in childhood may require invasive surgery. In addition, there is a high risk of recurrence. If the child's symptoms last longer than three months, treatment may be necessary.
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The pediatrician will order tests to diagnose the disease. Typically, a lumbar puncture is performed to obtain a sample of cerebrospinal fluid (CSF) from the child's spinal column. The CSF sample is then examined to look for tumor cells and the levels of glucose and protein in the CSF. A high amount of either may indicate the presence of a tumor.
