Atypical teratoid/rhabdoid tumor (AT/RT) is a type of cancer that affects the central nervous system. Although it is rare in adults, it is often mistaken for a more serious type of childhood cancer called medulloblastoma. A 2007 study conducted by the Pediatric Oncology Group evaluated the symptoms, prognosis, and survival of patients with AT/RT.
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Atypical teratoid/rhabdoid tumors are diagnosed through spinal cord and brain scans. A physical exam will check for any abnormalities or lumps. The doctor will also perform a neurological exam, which will assess the ability of the patient's muscles to walk and nerve function. The neurologic exam is an important part of the diagnostic process, as it will provide the doctor with information regarding atypical teratoid/rhomboid tumor symptoms and prognosis.
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Although the prevalence of AT/RT is rare, it is important to understand that the symptoms of the disease can be similar to those of a normal brain tumor. The atypical teratoid/rhabdoid tumor has many possible causes and can present symptoms in children as young as two years of age. It is best to seek diagnosis as early as possible so as to avoid any complications.
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PatientsLikeMe.org is an online community for individuals who have atypical teratoid/rhabdoid tumor. These forums can provide helpful information and support to individuals facing a diagnosis of atypical teratoid tumor. The forum is a great place to learn about other people who have had the same condition. If you'd like to learn more about the symptoms of AT/RT, please visit PatientsLikeMe.
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Because the symptoms of AT/RT may vary from patient to patient, it is important to understand the cause of your symptoms and to seek medical treatment if necessary. In addition, genetic factors and age may influence the risk of this disease, which can be fatal in young children. The diagnosis of an AT/RT can be made through a biopsy and removal of the tumor and spinal cord.
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An atypical teratoid/rhabdoid tumor can occur at any age. There are a variety of risk factors for this disease. However, the symptoms of this tumor are not confined to children. During the early stages, the patient may experience other symptoms. If the patient does not show any signs of atypical teratoid tumor, the tumor may be benign. It may be mistakenly diagnosed as a type of atypical teratoiid tumor.
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At-risk individuals are at increased risk for AT/RTs. Symptoms can be a result of atypical teratoid tumour or a recurrent tumour. If these symptoms are present, consult a pediatrician or neurooncologist. If the tumor is growing in the central nervous system, it may have spread to other areas.
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Atypical teratoid/Rhabdoid tumors are highly aggressive and resemble rhabdomyosarcoma. Most cases of ATRT occur in children. The risk of developing the disease is high in the early stages. Atypical teratoid/rhabdoid tumors are highly rare, but can occur in siblings. Atypical teratoid tumors are uncommon, and are usually inherited.
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An MRI can be performed to diagnose atypical teratoid tumor. During the examination, a neurologist will check the brain and spinal cord for signs and symptoms of the disease. During the examination, he will check for any symptoms that are unusual for the patient and may point to an underlying problem. MRIs may be necessary if the tumour has spread to the spine.
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At-risk patients may experience pain, a fever, and a lack of appetite. The symptoms of an AT-RRT are similar to those of other types of pediatric teratoid tumors, but have unique characteristics. They are more aggressive than MRTs, but are still not considered cancerous. Atypical teratoid/Rhabdoid tumors can also cause seizures, and can even cause death.
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Because AT/RT is so rare in children, there is no standard treatment for the disease.
Currently, most children with AT/RT undergo intensive multimodality treatments. Radiation therapy may be the only option for the child with AT/RT. Surgical resection is difficult and can have an adverse effect on survival. Several patients are at risk for at least two or three of these symptoms.
