Benign ependymoma (Q107627): Difference between revisions
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CID11:ID_338821956 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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Latest revision as of 14:38, 17 August 2026
Ependymoma is the most frequent intramedullary tumour in adults (but accounts for only 10-12% of pediatric central nervous system tumours), and can be benign or anaplastic. Ependymoma arise from the ependymal cells of the cerebral ventricles, corticle rests and central canal of the spinal cord, and manifest with variable symptoms such headache, vomiting, seizures, focal neurological signs and loss of vision and that can cause obstructive hydrocephalus in some cases.
| Language | Label | Description | Also known as |
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| default for all languages | ID_338821956 |
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| English | Benign ependymoma |
Ependymoma is the most frequent intramedullary tumour in adults (but accounts for only 10-12% of pediatric central nervous system tumours), and can be benign or anaplastic. Ependymoma arise from the ependymal cells of the cerebral ventricles, corticle rests and central canal of the spinal cord, and manifest with variable symptoms such headache, vomiting, seizures, focal neurological signs and loss of vision and that can cause obstructive hydrocephalus in some cases. |
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CID11:ID_338821956
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dki-india-ID_338821956
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Concluído
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16 August 2026
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