Atypical teratoid/rhabdoid tumor (ATRT) symptoms vary from patient to patient. They depend on the size, location, and morphology of the tumor. Some of the symptoms can be similar to other illnesses or conditions. For these reasons, it is important to seek medical attention if you notice any of these signs or symptoms in your child.
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The atypical teratoid/rhabdoid tumor is a type of malignant tumour that originates in the brain and represents one to two percent of all children with brain tumours. While it is rare, atypical teratoid rhabdoid tumors can also affect adults. Because of its severity, survival times can range from a few months to a few years. Only about 30% of patients live for 5 years.
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Atypical teratoid rhabdoid tumor is caused by mutations in certain genes. These mutations occur spontaneously or are inherited. In 85% of cases, ATRT is associated with a specific mutation. It is unknown what causes this change, but if a child develops this gene mutation during adolescence, they have an increased risk of developing other forms of the tumor.
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The most common symptoms are seizures, tremors, and weakness. If the child develops these symptoms, they should seek medical attention immediately. Atypical teratoid/rhabdoid tumor is extremely rare in children, occurring in about 10% of children with brain tumours. These benign tumors usually begin in the brain and spread to other parts of the body.
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Primary teratoid rhabdoid tumors are classified as embryonic tumours. They develop in the brain or spinal cord. They may arise anywhere in the central nervous system. Atypical teratoid rhabnoid tumours tend to develop in the central nervous system. They are often recurrent and inoperable. Acutely, they are not asymptomatic.
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Testing for atypical teratoid rhabdoid tumors involves several procedures, including a physical exam. A neurological exam is performed to check for signs of the disease and whether the patient is experiencing any unusual symptoms. A doctor will also perform tests to determine the functioning of the brain stem. Its presence can cause a number of complications and atypical teratoid/rhabdoid tumor can be fatal.
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Atypical teratoid/rhabdoid tumors can cause symptoms in children. The symptoms of ATRT may be similar to those of rhabdomyosarcoma, although they may be different. If you suspect atypical teratoid tumor, you should seek medical attention as soon as possible. A diagnosis is the first step in battling the disease.
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At its most common stage, AT/RT causes a variety of complications in children. Depending on the location and morphology of the tumor, it may cause the child to develop a pronounced headache. The symptoms of AT/RT may vary from patient to patient, but symptoms can include problems walking, losing balance, and other physical changes. It is important to seek medical attention for these early signs if they develop in the brain.
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Atypical teratoid rhabdoid tumors are rare childhood cancers that have a genetic mutation in the ATRT gene. The genetic mutation can be inherited or spontaneous and can affect the patient at any age. If it is inherited, children with this type of ATRT are at risk for other types of cancer. Parents often discuss clinical trials with their child. These trials can help them determine if the symptoms are indicative of a possible condition.
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While atypical teratoid/rhabdoid tumor symptoms in children are rare, they can occur in adults as well. The majority of cases of atypical teratoid tumors are benign and do not require treatment. The symptoms are often mild and can be misinterpreted as a result of other health problems. However, the earliest possible diagnosis is recommended.
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Atypical teratoid/rhabdoid tumor symptoms differ from patient to patient. The disease usually starts in the kidney or spinal cord. If the tumor develops in the CNS, it can cause a variety of neurological complications, including impaired coordination. A diagnosis requires the removal of the entire tumor and a biopsy. During the surgery, the tumor will be removed.
