Chordoma in Childhood Symptoms - Oren Zarif - Chordoma in Childhood
Most cases of chordoma in children are diagnosed in adults between the ages of 40 and 70. However, about five percent of cases are diagnosed in children. This cancer occurs in both males and females equally. The most common presenting symptoms are headache, diplopia, and difficulty swallowing. The disease has no known cause or symptoms, but the symptoms can be subtle. For this reason, it is important to identify the symptoms of chordoma in childhood as early as possible.
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When a child is diagnosed with chordoma, the best treatment is surgery. The tumor is surgically removed and the remaining tissue is resected. In severe cases, radiation therapy and proton beam radiation may be used to remove the tumor and preserve the nerves. The patient may also undergo gene testing in a clinical trial, which will enable doctors to determine whether a certain gene is altered. If this happens, the treatment will be tailored to that particular gene.
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Children with chordomas are often found in the skull and spinal cord. In the womb, a thin bar called the notochord runs down the baby's back. It supports the spine as it grows. However, before the child is born, this notochord will disappear, and chordoma will begin to form in the spinal cord and skull. The development of this tumor is the result of a change in the notochord gene.
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In the absence of other symptoms, the child will need to have a biopsy of the affected area. A biopsy is the only way to diagnose a chordoma. The doctor will take a sample of tumor cells and study them under a microscope to find out if they are cancerous. A blood test and bone scan will also help determine if the tumor has spread to other parts of the body.
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As a child grows, the notochord shrinks. In the womb, the notochord is thin and supports the spine. Before the baby is born, the notochord will disappear. Once a baby is born, the notochord cells will continue to divide. The notochord is very important to the health of a child, so a diagnosis of chordoma is necessary.
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If your child has a chordoma in the skull, it is important to get it checked by a doctor. This tumor will have no other symptoms in the early stages, but it can cause serious problems if it is not treated in time. Your child's doctors will have to determine the cause of the chordoma, and will need to perform tests to determine the best treatment. If you suspect your child has a chordoma, you should consult your pediatrician as soon as possible.
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Surgical intervention is the first option for chordoma treatment. The aim of this surgery is to reduce the size of the tumor and to obtain a complete resection. The surgeon will try to keep the tumor residues away from nervous and vascular structures. While surgical procedures for chordoma in childhood are rare, it is best to consult a doctor immediately if you notice any symptoms. In many cases, the cancer can be treated with chemotherapy.
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In very young children, a chordoma may not be visible, but it may cause pain. It is usually associated with poor vision. The disease may also affect the spine. For children under five years, the symptoms of chordoma include increased intracranial pressure and a decreased ability to see. The occurrence of a chordoma in children should be suspected as soon as possible. If a child has a chordoma in their skull, they should visit their doctor immediately.
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As with most tumours, the symptoms of a chordoma in childhood may vary. If the chordoma in the head blocks the flow of cerebrospinal fluid (CSF), the condition is called hydrocephalus. This condition can cause several other symptoms, depending on the age of the child. It can affect the child's ability to see and balance. A chordoma in the neck can also cause headaches and hoarseness.
