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A Case of Infantile Ganglioglioma Tetsuhiro KITAHARA 1 , Masami FUJII 1 , Junta MOROI 1 , Kouji KAJIWARA 1 , Haruhide ITO 1 1Department of Neurosurgery, Yamaguchi University School of Medicine Keyword: Ganglioglioma , Infant , CT , MRI , Synaptophysin pp.1111-1115
Published Date 1995/12/10
DOI https://doi.org/10.11477/mf.1436901129
  • Abstract
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Gangliogliomas are common in childhood, but rare in infancy. The authors report a rare case of ganglio-glioma who had an initial episode of complex partial seizure in fnfancy. A two-year-old girl was admitted for the surgical treatment of intractable seizures. She pre-sented with an initial episode of seizure at two months old. The CT scan at 2 months old showed a slight high-density tumor in the left medial temporal lobe. However, she had no treatment because she had no sei-zure since then and her psychomotor development was normal. She was treated with anticonvulsants from 1 year and 10 months old since seizures recurred. She was admitted to our ward at 2 years old because the frequency of seizures increased. Plain CT on admission showed an enlarged high density mass in left medial temporal lobe. The T1 weighted images of MRI de-monstrated the mass to be isointense compared with the cortex, with homogeneously contrast enhancement. Total removal of the tumor was performed and histolo-gical diagnosis was ganglioglioma. She is seizure-free after surgery and synaptophysin was useful for the his-tological diagnosis. This case may indicate that gan-gliogliomas can be a congenital brain tumor which slowly enlarges.


Copyright © 1995, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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