A child with childhood rhabdomyosarcoma may experience a range of unpleasant symptoms. The most common of these is pain and stiffness in the joints. If the condition has spread to the neck, it may require surgery. Treatment options vary from chemotherapy to surgery. In many cases, however, children can be treated with surgery. A lumbar puncture may be necessary. A doctor will insert a thin needle into the lower back, through which cerebrospinal fluid is sucked out. This sample is tested for the presence or absence of tumors.
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The first step in treatment is determining the type of cancer. Childhood rhabdomyosarcoma is categorized by its stage, which describes how widespread the cancer is. It is important to note that children with localized rhabdomyosarcoma have an excellent chance of long-term survival. Survival rates will vary, however, depending on the size and location of the tumor.
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Other childhood RMS symptoms include swelling and a growing mass. This depends on the primary tumor. Children with tumors in the reproductive or urinary tract may experience blood in the urine, difficulty urinating, and/or facial pain. Children with tumors in the base of the skull may have difficulty breathing, blurred vision, or facial asymmetry. In addition to these, a swelling in the orbit can be a symptom of RMS.
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A child may have no noticeable symptoms or show no signs at all. Regardless of the symptoms, a doctor can use blood and urine tests to determine the cause of the tumor. A doctor can also order an X-ray to see if there is an active tumor. An X-ray is used to examine the affected area, using radiation to create a picture of the affected area. Sometimes, rhabdomyosarcoma may not have any specific symptoms.
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Childhood Rhabdomyosarcoms are rare and are rarely caused by environmental factors. Some tumors are known to develop in the fetus, and are referred to as rhabdomyoblasts. These cells develop into muscle and are characterized by specific chromosome abnormalities. Patients with rhabdomyosarcoma are usually diagnosed during their childhood, but it can also occur in adults.
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Treatment options for childhood rhabdomyosarcoma depend on where the cancer is located and whether it is local or metastatic. Surgery is typically the first treatment option, but other treatments may be necessary for some children. Children with this cancer typically require surgery to remove it. Surgical methods used by CHOP surgeons may include the use of radiation and chemotherapy. While these treatments may result in complications, the majority of patients will experience significant reductions in pain and swelling and a return to normal activity.
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The side effects of treatment for childhood rhabdomyosarcoma can be severe, but they are rarely life-threatening. Some common side effects may occur during treatment, including hair loss, fatigue, nausea, and increased susceptibility to infection. Treatment can also cause side effects that persist for years after treatment. However, long-term side effects may include early onset of heart disease, early heart disease, and an increased risk of developing another cancer.
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During a biopsy, a small sample of tumor tissue is removed and tested for cancer cells. Children with aggressive forms of childhood rhabdomyosarcoma should receive intensive treatments only if the disease is already advanced. Recent advances in molecular research have helped to identify the genetic alteration that determines a positive prognosis in the disease. This alteration is more important than morphological characteristics.
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The next section of the guide is Diagnosis. In this section, the doctor will explain how to diagnose the symptoms of Childhood Rhabdomyosarcoma. The sections can be selected by using the menu. After the diagnosis, the patient will receive an appropriate treatment. For children under the age of five, there is a 90 percent chance of cure. However, in children under the age of nine, treatment for childhood Rhabdomyosarcoma may require chemotherapy, radiation, or surgery.
