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Atypical Teratoid/Rhabdoid Tumor Symptoms - Oren Zarif - Atypical Teratoid/Rhabdoid Tumor

  • Writer: Oren Zarif
    Oren Zarif
  • Feb 20, 2022
  • 3 min read

Although atypical teratoid/rhabdoid tumors are rare, they are often inherited. About 90% of all cases are related to a mutation in the gene SMARCB1, which is involved in the development of these tumors. The causes of this condition are unclear, but children with the mutation are at an increased risk for developing other types of brain tumors.

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Atypical teratoid/rhabdoid tumors are usually found in children under three years of age. They are also found in older children and adults, but their symptoms are similar to those of other conditions. There are several general symptoms associated with this condition, which may be present in some patients. A doctor can perform a biopsy to determine the cause of your condition and suggest a course of treatment.

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The disease is genetically-related. Certain genes may increase your risk. However, these risk factors do not assure that your child will develop the condition. Regardless of whether or not your child has a gene mutation, you should talk to your doctor to learn more about possible symptoms and possible treatments. Atypical teratoid/rhabdoid tumors can affect anyone, so it's important to discuss your risk with your pediatrician.

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Atypical Teratoid/Rhomboid Tumor is a rare central nervous system tumor. Although AT/RT typically occurs in children under three years old, it can affect adults as well. Approximately half of AT/RTs form in the brain stem or cerebellum. Ninety percent of all AT/RTs are caused by mutations in the INI1 gene.

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If you have been diagnosed with AT/RT, you need to seek medical advice immediately. This tumor is a type of brain tumor that affects the central nervous system. Moreover, it can spread throughout the body, causing a variety of symptoms. A doctor should also be able to determine the exact cause of your tumor. If the tumour is in the central nervous system, you should consult your pediatrician.

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Atypical teratoid/Rhabdoid tumors are aggressive, noninvasive tumours of the central nervous system that begin in the cerebellum or brain stem. These tumours typically develop during childhood and usually appear by the age of three. Because they are recurrent, they are classified as atypical teratoid rhabdoid tumors, and the symptoms they cause, are very similar to those of non-recurrent rhabdoid tumors.

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Atypical teratoid/Rhabdoid tumors are rare and are usually diagnosed in children under three years of age. The disease can occur in adults and children of any age. If a child has symptoms of AT/RT, he or she should seek medical care as soon as possible. Acutely ill health or pain in the spinal cord should be treated immediately.

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If you suspect you have an atypical teratoid/rhabdoid tumor, a physician will examine the symptoms and determine the appropriate course of treatment. The tumors will be small in size, and your doctor may recommend surgery, chemotherapy, or radiation therapy. It is important to discuss your symptoms with your pediatrician, as well as your family and medical history to determine the best course of action.

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Acute teratoid rhabdoid tumor symptoms may include persistent pain and swelling. Acute rhabdoid tumor symptoms are not life-threatening, but they may be accompanied by other health problems. In addition to the signs and symptoms, atypical teratoid/rhabdoid tumors may be accompanied by other signs of illness.

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Early diagnosis is essential for a good prognosis. An atypical teratoid/rhabdoid tumor is an uncommon type of brain tumor, but it can be present in adults. Atypical teratoid rhabdoid tumor symptoms vary from patient to patient. Your doctor may diagnose you with an atypical teratoid rhomboidal tumor as an adult or a pediatrician, or you may even have the condition before it starts to affect your child.

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Symptoms of atypical teratoid rhabdoid rhabnoid tumours in children are often difficult to distinguish from those of other types of brain tumours. Depending on the size and location of the tumour, symptoms may be very similar to those of another type of tumor. If you are concerned about your child's symptoms, visit your pediatrician as soon as possible.

 
 

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