Atypical teratoid/rhabdoid tumor symptoms vary from person to person and can be difficult to identify without proper diagnosis. Fortunately, this type of brain tumor is rare and only affects a small percentage of children with brain tumors. Symptoms of ATRT can include: increased appetite, fever, vomiting, diarrhea, and a fever-like feeling.
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Treatment for Atypical Teratoid/Rhomboidal Tumors is individualized and may include various treatments. Surgical removal of the tumor is one of the most common treatments. During surgery, the surgeon will remove as much of the tumor as is safe. Chemotherapy is another treatment option. This form of treatment uses powerful medicines to kill cancer cells and prevent them from dividing. It can be given by mouth or as a combination of different types of drugs. Radiation therapy may also be used to destroy the tumor by using high-energy X-rays or other forms of radiation.
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The first treatment for Atypical Teratoid/Rhomboids is a surgical procedure. The cancer is usually in the central nervous system. The atypical teratoid/Rhabdoid tumor has been diagnosed in children as young as age three. A diagnosis of AT/RT can be difficult if a child has had repeated tests to confirm the diagnosis.
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Atypical Teratoid/Rhomboid Tumor (ATRT) is a very rare form of brain cancer. Although it typically occurs in children, it can also occur in adults. It is a challenging condition to treat, with survival rates ranging from a few months to several years. Thankfully, many patients with AT/RT can survive with the help of chemotherapy.
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Atypical Teratoid/Rhomboid tumors can be found anywhere in the central nervous system. They are very aggressive tumors of the central nervous system that typically occur in the cerebellum and brain stem. Atypical teratoid rhabdoid tumor symptoms can include confusion and pain. If your child has a history of AT/RT, he or she may have difficulty understanding the diagnosis.
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Atypical teratoid/Rhabdoid tumors are very rare neoplasms of the central nervous system. Most cases affect children younger than two years of age. They can be difficult to diagnose, but they do appear in a variety of sizes and locations. While symptoms can vary, they typically include a mass in the posterior fossa.
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The symptoms of ATRT can be characterized by an abnormal growth of rhabdoid cells in the brain. The symptoms are usually asymmetric and non-symmetrical in appearance. They are generally benign but may cause neurological damage. If the symptoms persist, the patient should seek medical treatment. If ATRT causes seizures, he should be monitored immediately by a physician.
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Depending on the location, this tumor can be benign or malignant. In severe cases, atypical teratoid/rhabdoid tumors may require surgery. Atypical teratoid/rrabdoid tumours can spread to the spinal cord and brain, so it is important to have a complete diagnosis. Acute teratoid/rhabdoses are often difficult to treat.
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The symptoms of an atypical teratoid/rhabdoid tumor depend on the size and location of the tumor. The tumor may produce different symptoms than a typical teratoid tumor, so a doctor should evaluate the child's symptoms to make sure there isn't another condition that is causing it. If the signs of an AT/RT are present, the child should be seen by a physician as soon as possible.
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Oftentimes, the atypical teratoid/rhabdoid tumor is an inherited disease. It may occur in the spine, arms, or legs, and may affect the brain and other parts of the body. In most cases, atypical teratoid tumor symptoms do not vary, but may include a morning headache, loss of coordination, and trouble walking.
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Typically, the Atypical Teratoid/Rhombid Tumor symptom is not an indication of an underlying disease. In some cases, the symptoms of atypical teratoid/rhabdoid tumor are a symptom of another condition. In some cases, the Atypical TERA/RH tumor can develop in the brain, and may cause symptoms or even death.
