Atypical teratoid/rhabdoid tumors are rare cancers that arise from the abnormalities of genes. The causes of atypical teratoid rhabdoid tumors (ATRT) are unknown. The mutation that results in this cancer is inherited in about 90% of cases. Children who inherit this mutation may have a greater risk for developing other types of brain tumors, including malignant glioma.
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Atypical teratoid/rhabdoid tumor symptoms are similar to those of other teratoid tumours. A typical ATRT begins in the cerebellum and spinal cord but can occur anywhere in the brain. The growth rate of ATRTs is rapid and they spread throughout the central nervous system. Atypical teratoid/ recurrent rhabdoid tumors are also known as atypical teratoid/r-rhabdoid tumours.
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Atypical teratoid/rhabdoid tumor symptoms vary from person to person, but they are associated with inherited changes in SMARCB1 or SMARCA4 genes. Because of this association, genetic counseling may be recommended for patients with AT/RT. Symptoms vary widely from patient to patient, but they may include a nagging morning headache, unusual sleepiness, loss of balance or coordination, and other symptoms.
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In addition to its aggressiveness, ATRTs are often present in adults. An early diagnosis of ATRT should be possible. Symptoms may include: a rash, fever, seizures, and abdominal pain. A CT scan and biopsy are important to diagnose an ATRT. In some cases, the tumor may be found on a bone x-ray. While not fatal, the symptoms may be confusing and warrant a visit to a physician.
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Atypical teratoid/Rhabdoid tumors can affect any part of the central nervous system. The most common location for ATRT is the cerebellum. They tend to spread throughout the central nervous system. Treatment is usually based on the spread of the cancer, and it may be surgically removed. The patient may experience vomiting or diarrhea. Atypical teratoid/rhabdoid tumors are treated with chemotherapy or surgery.
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Symptoms of ATRT are similar to those of atypical teratoid tumors. Those with these tumours will likely have an increase in the size of their brains. The disease can also spread to other areas of the body, which is why early detection is essential. It is important to discuss symptoms with your doctor. Your child may have atypical teratoid/rhabdoid tumor.
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If you have atypical teratoid/rhabdoid tumor, you should have a biopsy to confirm the diagnosis. The tumor can spread to other parts of the body and cause other symptoms. Atypical teratoid/rhombodysis is a very common form of childhood brain cancer. The only sign of malignancy in children is atypical teratoid tumor.
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Most cases of Atypical Teratoid/Rhomboids begin in the brain. These tumours start in the central nervous system, such as the cerebellum. They cause a lot of symptoms and must be diagnosed by a physician. If you see the symptoms of an atypical teratoid tumor, you should go to the doctor immediately.
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An AT/RT is a rare cancer of the central nervous system. Symptoms of ATRT can include a whitish appearance of the tumour or the onset of a rash or weakness. Typically, atypical teratoid/rhabdoid tumors present with a white patch on the cerebellum. Atypical teratoid/Rhabdoid tumours are typically diagnosed in childhood, but can also be diagnosed in adults.
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While an AT/RT is rare, it can be contagious. It is often found in young children. In some cases, it can be spread to other parts of the body. Atypical teratoid/rhabdoid tumors are often asymptomatic. However, atypical teratoid tumors can lead to an infection, which could eventually lead to death.
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Atypical teratoid rhabdoid tumors can develop in the central nervous system. The brain and spinal cord are often involved in this condition. The occurrence of this tumor in young children is usually attributed to genetic changes in the parents. The child's age at diagnosis will determine the prognosis of the child. If the tumour is detected in the early stages, the prognosis will be better.
