{"id":11122,"date":"2025-07-27T10:55:57","date_gmt":"2025-07-27T08:55:57","guid":{"rendered":"https:\/\/valintermed.com\/?p=11122"},"modified":"2025-07-27T10:55:57","modified_gmt":"2025-07-27T08:55:57","slug":"ependimoma","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/ependymoma\/","title":{"rendered":"Ependymoma"},"content":{"rendered":"
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Ependymoma is a tumor arising from the ependymal cells that line the ventricles of the brain and the central canal of the spinal cord. It is a relatively rare form of central nervous system (CNS) tumor and occurs in both adults and children. Ependymomas are classified by grade into three main groups: anaplastic ependymoma, low-grade ependymoma, and myoependymoma. The clinical manifestations of this disease vary depending on the location of the tumor and may include neurological symptoms such as headaches, seizures, hearing or vision loss, and changes in motor function. The study of ependymoma is an important part of oncology and neurosurgery, which requires a multifactorial approach to diagnosis and treatment.<\/p>\n

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