1985
DOI: 10.1007/bf01418803
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Gangliocytoma of the pineal body a case report and review of the literature

Abstract: Ganglion cell tumours are mostly seen in children and young people, but they are extremely rare, accounting for 0.1-0.5% of all brain tumours. It usually occurs in the floor of the third ventricle and the temporal lobe. Recently we have experienced a pineal gangliocytoma, probably the first ever seen in Japan and the fourth case in the world, and have succeeded in a total removal of it. The case concerns a 51-year-old man who suffered from intermittent blurred vision and headache of 3 years' duration. CT showe… Show more

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Cited by 13 publications
(10 citation statements)
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“…Bilateral hearing and vision impairment has been frequently associated with pineal tumors [5][6][7][8][9].…”
Section: Discussionmentioning
confidence: 99%
“…Bilateral hearing and vision impairment has been frequently associated with pineal tumors [5][6][7][8][9].…”
Section: Discussionmentioning
confidence: 99%
“…Em 1930, Courville publicou a primeira casuística, com 20 pacientes portadores de ganglioglioma e extensa revisão, estabelecendo, a partir de então, essa denominação na literatura 2 . Na revisão da literatura foram encontrados apenas oito casos de ganglioglioma da região da pineal publicados [5][6][7][8][9][10][11][12] , que com o atual relato perfazem nove casos. Horrax e Bayle, em 1928, descreveram o primeiro caso (ganglioneuroma) 9 .…”
Section: Discussionunclassified
“…Assim, os gangliogliomas da região da pineal são tumores extremamente raros 5 . Na revisão da literatura foram encontrados apenas oito casos publicados [5][6][7][8][9][10][11][12] , nenhum deles no Brasil.Tendo em vista a raridade desta lesão decidiu-se pela realização do presente estudo, no qual é relatado o caso de paciente de 14 anos, masculino, com ganglioglioma da região da pineal e são revisadas as características clínicas, radiográficas, histopatoló-gicas, além do tratamento e do prognóstico de tais tumores. CASO Trata-se de paciente de 14 anos, masculino, branco, com história de, aos seis anos de idade, ter iniciado quadro de cefaléia holocraniana, episódica, que aliviava com analgésicos convencionais.…”
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“…MRI obtained at that time demonstrated no further progression of the lesion. Neuronal and mixed neuronal-glial tumors are extremely rare, accounting for 0.1% to 0.5% of all brain tumors 3 . They are mostly seen in children and young people 3 , but the age of incidence ranges from 2 months to 80 years 1 .…”
Section: Casementioning
confidence: 99%