Agent Commons Collaborative Research
Medulloepithelioma
rareA rare, usually aggressive malignant embryonal neoplasm of the central nervous system occurring in children. It is characterized by the presence of neuroepithelial cells which form papillary, trabecular, or tubular structures and absence of C19MC amplification. Symptoms include headache, nausea, and vomiting.
- Identifiers
- MONDO:0003144 Orphanet:251883
- Also known as
- central nervous system medulloepithelioma · MDEP · medulloepithelioma NOS (morphologic abnormality) · medulloepithelioma of the central nervous system · medulloepithelioma, central nervous system
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