While it's not common in children, an atypical teratoid/rhabdoid tumor may be present in your child. This brain tumor represents approximately one percent of all paediatric brain tumours, although it can also develop in adults. While the disease is not curable, patients with this condition are usually able to live for several months or even years after diagnosis.
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There are many symptoms that a child with this tumor may experience, some of which start months or years before the diagnosis. These signs should be discussed with the child and his or her physician. Treatment for an atypical teratoid/rhabdoid tumor may include surgery. For more information on ATRT, visit the General Information section of the website.
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Atypical Teratoid/Rhomboid Tumor (ATRT) is a rare type of brain cancer. It normally occurs in children, but it can occur in older children and adults. 90% of ATRTs are caused by mutations in the INI1 gene, a gene that produces proteins that control the tumor's growth. This defect in the ATRT gene makes the tumor grow uncontrolled.
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Atypical teratoid/rhabdoid tumor symptoms vary. Typically, the tumor will form in one part of the body at a time. Some patients may experience both CNS and peripheral nerve-related symptoms. If the ATRT is found in the CNS, a biopsy will be needed to determine where the tumour is located. The doctor will perform tests that will determine whether it is affecting the brain or spinal cord.
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Atypical teratoid/rhabdoid tumors are often classified as embryonal tumours. They develop from embryonic stem cells in the brain after birth. The cancerous cells may eventually divide and spread throughout the central nervous system and cause an atypical teratoid tumor. It may also occur in a central nervous system, such as the spinal cord.
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The most common symptoms are headache, fever, and tingling in the arms and legs. At least one of the patients may experience seizures. At least one part of the body will have at least one symptom. In addition to headaches and pain, Atypical Teratoid/Rhhabdoid Tumors can spread to other parts of the body.
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Atypical teratoid/Rhabdoid tumors are uncommon tumors of the central nervous system. Generally, the disease affects children younger than three years old, although it has also been reported in adults. Clinical presentations of AT/RT vary by location, and atypical teratoid/rhabdoid tumors can be benign or malignant.
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The majority of atypical teratoid/Rhabdoid tumors are rare and are usually present at an early age. Most cases are found in young children, and the earliest onset is around age two. The symptoms of an atypical teratoid rhabdoid tumor are similar to those of other atypical teratoid tumors.
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The symptoms of ATRT are common and vary according to the location of the tumor. The tumors can be localized in the cerebellum or in the brain stem. The disease usually has a slow, progressive growth and causes severe impairment. However, the signs and symptoms of ATRT may vary depending on the location of the tumor in the body. If the tumors are localized in the spinal cord, they may spread outside the area and spread to other parts of the body.
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ATRT is a rare neoplasm that has a very poor prognosis. It is often mistaken for a medulloblastoma in young children. In the United States, it is rare to see an adult ATRT. It is, however, possible to find an ATRT in the brain. It is important to discuss any potential symptoms with a doctor.
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Atypical teratoid/Rhabdoid tumors start in the spinal cord and brain. Most of these cancers begin in the cerebellum, but they may occur in other areas of the brain. They are fast-growing and tend to spread throughout the central nervous system. If they are found in the cerebellum, they may be called atypical teratoid rhabdoid tumours.
