Atypical teratoid rhabdoid tumour of brain (Q91122): Difference between revisions
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Neoplasia embrionária maligna agressiva originada do sistema nervoso central. É composta por células com grande núcleo excêntrico, nucléolo proeminente e citoplasma abundante. Pode estar associada à perda do cromossomo 22. A grande maioria dos casos ocorre na infância. Os sintomas incluem letargia, vômitos, paralisia dos nervos cranianos, cefaleia e hemiplegia. | |||
| description / en | description / en | ||
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. | |||
Revision as of 18:07, 15 August 2026
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.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1864152995 |
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| English | Atypical teratoid rhabdoid tumour of brain |
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. |
