Chordoma in Childhood Symptoms - Oren Zarif - Chordoma in Childhood
Although chordomas typically affect adults, about five percent of cases occur in children. They are most common in males. Most cases are noninvasive and are usually detected during childhood. If you or a child suspects that they have this condition, contact your physician. Early detection and treatment can prevent complications and provide a high chance of a cure. To find out if your child has a chordoma, read on for more information on this disease.
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The first step in treating chordoma is surgery. Surgical objectives include removal of the whole tumor and minimal secondary effects. The objective of surgery is to reduce the tumour volume and achieve complete excision. Surgical techniques may involve a biopsy of the tumor to identify any genetic changes. This allows doctors to customize a treatment plan based on the patient's specific needs. If you suspect your child has a chordoma, you will likely undergo surgery.
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Your doctor will likely recommend a combination of therapies, including surgery and radiation therapy. Your doctor will recommend a combination of treatments to determine which is the best fit for your child. Depending on the stage of your child's cancer, a variety of chemotherapy and proton beam radiation therapies may be used. Your doctor will also be able to recommend a clinical trial for your child, which will test for any genetic changes that may be present.
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Because chordoma is difficult to detect, treatment is individualized. The goal of treatment is to eliminate the tumor entirely. However, this approach has many side effects. Because radiation damages healthy tissue, it does not remove the entire tumor. Because of this, doctors often combine radiation and surgery, which lowers the chances of the disease coming back. In addition, after a successful treatment, doctors will perform MRIs every three months for up to a year, and you may need another surgery if you experience a recurrence of chordoma.
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Depending on the stage of the disease, your doctor may suggest surgery to remove the tumor. As you might have suspected, chordomas in childhood may be painful, requiring urgent treatment. During the first few weeks after diagnosis, you should see your doctor, as soon as possible. If the tumor is causing your child to have symptoms, consider undergoing surgery. Generally, pediatric surgery is the only option for removing the tumor, or undergoing an alternative treatment.
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Although chordoma in childhood is rare, it can come back after treatment. The best way to manage chordoma in children is to have your child evaluated by a pediatrician. The earliest diagnosis is at least three months old, and your doctor may want to follow up with the results to monitor your child's growth. A good plan should also be based on a comprehensive review of the literature.
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The most common symptoms of chordoma in children are pain, weakness, and vomiting. Depending on the location and size of the tumor, your child may experience a variety of symptoms. In some cases, a chordoma in childhood may lead to bowel and bladder problems. Other symptoms may include double vision, headache, and abnormal eye movements. When a chordoma in childhood is located in the skull base, a tumor may be more severe and the child will require surgery.
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While there are no definitive symptoms of chordoma in children, it is important to seek the right diagnosis early. A doctor may recommend surgery for childhood chordoma if there are other signs of the disease. The first treatment for this type of chordoma in children is surgery, which involves removing the tumor. After it has been removed, radiation therapy may be given to kill the remaining cancer cells.
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MRI or CT scans are required to diagnose chordoma. A physical examination will reveal the presence of a mass. MR scans are an excellent way to diagnose this disease. The imaging results will also help you determine the extent of the problem. If the mass is larger than two centimeters, it is likely that it is cancer. Fortunately, the tumor is rarely malignant. While it can recur after treatment, it is rare and will not recur.
