Atypical teratoid/rhabdoid tumor is a rare central nervous system tumor that is characterized by a specific mutation. The cause of this mutation is unknown. In most cases, it is inherited, and 90% of cases occur spontaneously. Children with this mutation are at increased risk of developing other brain and spinal cord tumors. While the underlying reason for the inherited mutation is unclear, it is important to note that genetics may play a role in the development of atypical teratoid/rabid tumors.
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The symptoms of ATRT include a mass in the posterior fossa, a recurrent tumor, and seizures. The tumour typically occurs in young children, but it can also affect adults. General symptoms of the condition can include pain, headache, and nausea. If the patient has other medical conditions, the symptoms can be attributed to those conditions. Atypical teratoid/rhabdoid tumor is most likely to be a recurrent teratoid tumour.
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Children with atypical teratoid/rhabdoid tumor may experience headaches and a fever. If a child has a family history of atypical teratoid tumor, a family doctor may suggest a MRI or CT scan. While these conditions do not increase the risk of developing the disease, they do raise it. The most common symptom of an Atypical TERATOID/Rhabdoid Tumor is a lump in the back of the knee. Atypical teratoid/rhomboids in children can be very painful.
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The most common symptom of ATRT is a symptomless, non-specific rash. Patients with an ATRT are prone to developing seizures. Other symptoms include a swollen or painful abdomen and fever. Atypical Teratoid/Rhombioid Tumor Symptoms vary from patient to patient. Treatment options and prognosis vary depending on the type of tumor.
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Children with certain genetic variations have an increased risk of developing an ATR. Atypical teratoid/Rhabdoid tumors have similar histology. Many children with AT/RT have two or three brain tumors. At least one will develop at least one. Fortunately, there are no known cures for this disease. Luckily, there are several treatments available for the disease.
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If your child develops ATRT, he or she should seek treatment as soon as possible. If the disease is advanced, your doctor may have to remove a portion of the affected organ. However, if you still have symptoms, he or she may recommend surgical intervention. Atypical Teratoid/Rhoid tumors can lead to death.
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Atypical Teratoid/Rhomboids are malignant tumors of the central nervous system. These cancers usually occur in the cerebellum or brain stem. They occur in children and account for two to three percent of childhood brain tumors. They are more common in men than in women, and are more common in boys than in girls. Symptoms of ATR can include an enlarged brain or spine.
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AT/RT is a rare central nervous system tumor, affecting a small percentage of children. These tumors are often mistaken for medulloblastoma in adults. Although atypical teratoid/rhabdoid tumor symptoms vary from patient to patient, the disease is generally diagnosed through a biopsy or surgery in the brain and spinal cord.
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Atypical teratoid/Rhabdoid tumor symptoms are often similar to those of a rhabdomyosarcoma and atypical teratoid tumor. Despite their similarity, the disease is highly uncommon and has no symptoms. It is best to consult a physician as soon as possible, as there are many symptoms associated with this condition.
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The main symptoms of ATRT are mainly based on imaging findings. The tumors may be hyperdense, with patchy enhancement and intratumoral hemorrhage. They may be calcified or contain primitive neuroepithelial tissue. There is no specific standard of treatment for AT/RT. PDQ's Cancer Information Summary provides comprehensive information for clinicians.
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Among children with this type of tumor, the standard treatment for atypical teratoid/rhabdoid tumor is not yet clear. Usually, a pediatric rhabdoid tumor will not grow in the skull or on the brain. In some cases, a diagnosis can be difficult to make because the tumor is not completely removed. The patient may need multiple treatments, including a stem cell transplant.
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