[An aggressive malignant embryonal neoplasm arising from the central nervous system. It is composed of cells with a large eccentric nucleus, prominent nucleolus, and abundant cytoplasm. It may be associated with loss of chromosome 22. The vast majority of cases occur in childhood. Symptoms include lethargy, vomiting, cranial nerve palsy, headache, and hemiplegia. ( NCI )]
UMLS (NCI) C1266184Atypical Teratoid/Rhabdoid Tumor
Central Nervous System Rhabdoid Neoplasm
Central Nervous System Rhabdoid Tumor
CNS Rhabdoid Neoplasm
CNS Rhabdoid Tumor
Malignant Brain Rhabdoid Neoplasm
Malignant Brain Rhabdoid Tumor
Malignant Rhabdoid Neoplasm of Brain
Malignant Rhabdoid Neoplasm of the Brain
Malignant Rhabdoid Tumor of Brain
Malignant Rhabdoid Tumor of the Brain
Primary Malignant Brain Rhabdoid Neoplasm
Primary Malignant Brain Rhabdoid Tumor
Primary Malignant Rhabdoid Neoplasm of Brain
Primary Malignant Rhabdoid Neoplasm of the Brain
Primary Malignant Rhabdoid Tumor of Brain
Primary Malignant Rhabdoid Tumor of the Brain
Rhabdoid Neoplasm of Central Nervous System
Rhabdoid Neoplasm of CNS
Rhabdoid Neoplasm of the Central Nervous System
Rhabdoid Neoplasm of the CNS
Rhabdoid Tumor of Central Nervous System
Rhabdoid Tumor of CNS
Rhabdoid Tumor of the Central Nervous System
Rhabdoid Tumor of the CNS