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A Multicentric Glioma Presenting Different Pathological Appearances : A Case Report Shougo KAKU 1 , Tohru TERAO 1 , Keisuke TAYA 1 , Toshihiro OHTUKA 1 , Toshihide TANAKA 1 , Satoshi SAWAUCHI 1 , Robert Tomohiko NUMOTO 1 , Shigeyuki MURAKAMI 1 , Mitsuhiro OHMURA 2 , Toshiaki ABE 3 1Department of Neurosurgery,Jikei University School of Medicine,Kashiwa Hospital 2Department of Pathology,Jikei University School of Medicine,Kashiwa Hospital 3Department of Neurosurgery,Jikei University School of Medicine Keyword: multicentric glioma , gemistocytic astrocytoma , anaplastic astrocytoma pp.501-506
Published Date 2004/5/1
DOI https://doi.org/10.11477/mf.1436100388

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  • Abstract
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 We report a multicentric glioma case which revealed different pathological appearances. A 45-year-old male had been admitted to our hospital complaining of an attack of transient sudden aphasia. On magnetic resonance imaging (MRI),T1-weighted images revealed a low intensity and T2-weighted images demonstrated a homogeneous high intensity abnormal mass in the frontal lobe,which was not enhanced with gadolinium. Removal of the tumor was performed through a right frontal transcortical approach in March,2002. Histological diagnosis was gemistocytic astrocytoma. The patient's condition was uneventful and postoperative MRI revealed a marked decrease in the volume of the tumor. A total of 54Gy radiation to the brain in the locality was performed. Four months after the initial surgery,the patient suffered from incomplete right hemiparesis. MRI showed a left parietal abnormal mass which had a ring formation enhancement after gadolinium administration. This Neuro-radiological examination demonstrated complete independence from the initial right frontal tumor. A second surgery which was concerned with cyst aspiration was carried out on August 10,2002. During the next month,a third operation for partial removal of a left parietal abnormal mass was performed. Histological diagnosis was anaplastic astrocytoma. The right frontal and left parietal tumors revealed neither continuous relation suggesting intracerebral invasion,nor dissemination through the subarachnoid space nor intracerebral metastasis. Our case was diagnosed as multicentric glioma with different pathological appearances,of which only 9 cases have been reported previously.


Copyright © 2004, 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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