Ganglioglioma
Mostrando 13-18 de 18 artigos, teses e dissertações.
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13. Ganglioglioma da medula espinhal: relato de caso
Os gangliogliomas são tumores raros do SNC, compreendendo apenas 2,7 a 3,8% dos tumores primários do SNC e as lesões medulares perfazem 7,6 a 14,3 % do total de gangliogliomas. O tratamento preconizado pela literatura é a ressecção total, ficando a radioterapia reservada apenas em casos de progressão da doença após a cirurgia ou em casos de lesões
Arquivos de Neuro-Psiquiatria. Publicado em: 2001-06
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14. Características clínicas, de neuroimagem estrutural e prognóstico cirúrgico de pacientes com tumor do lobo temporal e epilepsia
Este é um estudo retrospectivo de 21 pacientes com epilepsia e tumores do lobo temporal tratados cirurgicamente. A avaliação incluiu dados clínicos, eletrencefalográficos, de neuroimagem, anatomia patológica e seguimento pós-operatório. Eram 9 casos de ganglioglioma, 5 de astrocitoma pilocítico, 3 de ganglioneuroma, 2 de tumor neuroectodérmico dise
Arquivos de Neuro-Psiquiatria. Publicado em: 2000-12
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15. Desmoplastic Infantile Ganglioglioma: cytologic findings and differential diagnosis on aspiration material
BioMed Central.
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16. Gangliogliomas: clinical, radiological, and histopathological findings in 51 patients.
Clinical, radiological, and histopathological features of 51 surgically treated gangliogliomas were evaluated retrospectively. The most common presenting symptoms were epileptic seizures (47 patients (92%)). Focal neurological deficits occurred in 8% of the patients. The duration of symptoms at the time of operation ranged from three months to 45 years, mean
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17. Cerebral ganglioglio-neuroblastoma: an unusual brain tumour of the neuron series.
The pathology of an unusual intracranial neuroectodermal tumour of the neuron series in described and its possible histogenesis discussed. The tumour, in a child aged 5 years with an enlarged head since infancy, presented as a large solid intra-cerebral mass. Histological examination showed four types of cells; (i) the stroma, forming the bulk of the tumour,
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18. Long term survival with early childhood intracerebral tumours.
Three young adults are described who presented during early childhood with a seizure disorder due to an underlying intracerebral tumour. The tumours were excised incompletely 14-19 years later. The histological findings were those of a temporal lobe benign capillary haemangioblastoma (Case 1), parietal lobe subependymoma (Case 2), and parietal lobe gangliogl