Atypical teratoid/rhabdoid tumor (AT/RT) is a rare type of cancer that affects the central nervous system. Most AT/RTs occur in children younger than three years of age, but they can also develop in adults. About half of all AT/RTs originate in the cerebellum and brain stem, which control movement and balance. This type of cancer is rare, but it can be deadly.
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The first thing to know about AT/RT is that it can develop in different parts of the central nervous system. It usually begins in the brain and spreads to other parts of the central nervous system, including the spinal cord and brain. The most common sites are the sellar region and the cerebral hemispheres, and there may be evidence of widespread disease. Although it is difficult to identify the exact location of the tumour, doctors can perform a biopsy to detect if it is in the brain or spinal cord.
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Patients with Atypical Teratoid/Rhomboids should visit their doctor immediately. The symptoms associated with this type of tumor are based on the location of the tumor and its location. Most children will develop atypical teratoid/rhabdoid tumors during their childhood. It is not clear what causes these types of cancer, but it has been noted to be associated with a poor prognosis.
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Atypical Teratoid/Rhomboidal Tumor Treatment depends on the location and stage of the tumor. Surgery and chemotherapy are the most common treatments. However, radiation and chemotherapy are sometimes necessary in certain cases. The earliest diagnosis should be possible. Once the diagnosis is made, the next step is to treat the tumor with a treatment plan. Atypical Teratoid/RHMT Symptoms
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Tests to diagnose ATRT include spinal cord and brain tests. A physical examination will look for signs of the disease, such as lumps or unusual symptoms. The doctor will also ask about any other past illnesses and medical conditions. The neurological exam will examine the nerves and reflexes and will help determine the extent of the tumor. A CT scan is recommended to check the patient's condition.
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Atypical Teratoid/Rhombdoid tumors are rare tumors of the central nervous system. They occur in the cerebellum and brain stem and make up two to three percent of all childhood brain tumors. The most common type of ATRT is found in children between the ages of three and five. Atypical teratoid/Rhabdoid is most commonly diagnosed in children between the ages of three and seven years of age.
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Atypical teratoid rhabdoid tumour is an aggressive type of brain cancer. The survival rate for children is poor, but recent advances in therapy are improving this outlook. Parents are encouraged to discuss the options for clinical trials with their child's pediatrician. There are many options for treating ATRT. Atypical teratoid & Rhabdoid Tumor Symptoms
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Atypical teratoid rhabdoid tumors are embryonal tumours that originate in the brain and spinal cord. They tend to begin in the brain and spread to other parts of the central nervous system. Atypical teratoid t/R tumours may also be found in the spinal cord. This cancer is often inherited and has no cure. Atypical teratoid/Rhabdoid tumor symptoms are similar to those of other types of cancer.
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An ATRT is a type of aggressive brain tumor that affects the brain. It affects the cerebellum, which regulates movement. Besides the cerebellum, ATRTs may spread throughout the body. They may even affect the muscles of the limbs. The symptoms of an ATRT can vary, but they are the same as those of other types of cancer.
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Typical AT/RT symptoms include the presence of multiple rhabdoid tumors in the central nervous system. These tumors usually grow inside the cerebellum, which is an area of the brain that has been shaped by a single cell. Symptoms of an AT/RT can occur in all areas of the body, from the brain to the skin and heart.
