If your child is displaying the symptoms of Childhood Rhabdomyosarcomal syndrome, you may want to seek medical attention right away. Early detection of the cancer is crucial to a child's long-term survival. Listed below are some of the most important symptoms to watch out for. Those that are not present, however, may be a sign of an underlying condition.
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If your child has childhood rhabdomyosarcoma, there are two common treatment options. The first is surgery, which aims to remove the tumor while preserving the normal tissue of the affected area. The surgery may be performed by a neurosurgeon, otolaryngologist, or craniofacial surgeon. Patients may also undergo chemotherapy, which is a medicine that kills cancer cells and is given through an IV.
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Children with these cancers are at risk for a number of side effects, including severe pain and a delayed development. Fortunately, there are treatments for childhood Rhabdomyosarcoma that can relieve symptoms and ensure a child's quality of life. A comprehensive medical workup is necessary to determine the exact cause of the symptoms and determine the most effective treatment. Your child may need a needle biopsy to identify the cancer. If it is in the muscles, a doctor may perform a lumbar puncture to collect a sample of the fluid that surrounds the spinal cord and brain.
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When the tumor is located in the arms or legs, surgery is a popular treatment option. The surgery can remove the entire tumor, or part of it. Some patients may benefit from radiation therapy. The treatments also include surgery for genitourinary rhabdomyosarcoma. Children with rhabdomyosarcoma also undergo chemotherapy and radiation therapy. While the treatment options for this cancer depend on the type of tumor, most children with rhabdomyosarcoma survive for many years.
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Treatment for childhood rhabdomyosarcoma depends on the location and size of the tumor. Some symptoms may be similar to those of other childhood illnesses. However, a blood or urine test can help diagnose the condition. An X-ray is another way to detect a tumor. A scan uses radiation to take pictures of the affected area. When symptoms of Childhood Rhabdomyosarcoma are present, it is important to seek treatment early.
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Rhabdomyosarcoma in the head and neck is the most common form of childhood Rhabdomyosarcoma. It can cause difficulty urinating, blood in the urine, constipation, and a lump. It can also spread to the other parts of the body. Other symptoms of this disease include pain in the head, swelling of the ear, and sinus congestion.
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Children diagnosed with childhood rhabdomyosarcoma usually receive chemotherapy and radiation treatment. The type and location of the tumor will determine the type and stage of treatment. Treatment may include surgery, radiation therapy, and sometimes chemotherapy. Sometimes, surgery is not possible. Radiation therapy, however, may be used to shrink or stop the growth of abnormal cells. This treatment option is sometimes more effective. But it may not be appropriate for every child.
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Childhood rhabdomyosarcoma is a rare cancer. Early diagnosis and aggressive treatment is key. Children with rhabdomyosarcoma may qualify for clinical trials. If you have been diagnosed with the disease, talk with your pediatrician and urologic oncologist about your treatment options. The next step is finding a specialist. If you suspect that your child has RMS, contact your doctor immediately.
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The most common type of childhood soft tissue cancer, rhabdomyosarcoma can occur in any part of the body. The tumour can grow anywhere in the body, but most often in the head and neck. Children under age six are most commonly diagnosed with this type of cancer. Symptoms of childhood rhabdomyosarcoma may include swelling of an area, pain in the area, or a lump. If the tumor has spread, you will likely need a biopsy to confirm a diagnosis.
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There are two main types of childhood rhabdomyosarcoma, alveolar and embryonal. The latter tends to be more aggressive than the former, but they can occur at any age. Symptoms of rhabdomyosarcoma may vary from one child to another, depending on the size and location of the tumor. Symptoms vary from child to child, so it's important to seek medical attention as soon as possible.
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Although there is no known cause of childhood rhabdomyosarcoma, certain risk factors are associated with increased risks of developing this type of cancer. Children with a large birth weight and a high birth weight are at higher risk of developing embryonal rhabdomyosarcoma than children of normal birth weight. While childhood rhabdomyosarcoma symptoms are difficult to recognize, it is possible to identify the condition early.
