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Dysembryoplastic Neuroepithelial Tumor:A case report Hiroshi HASEGAWA 1 , Shoji BITOH 1 , Kentaro KOSHINO 1 , Jiro OBASHI 1 , Yasushi KOBAYASHI 2 1Departments of Neurosurgery, Osaka Koseinenkin Hospital 2Departments of Pathology, Osaka Koseinenkin Hospital Keyword: Dysembryoplastic neuroepithelial tumor , Ganglioglioma , Computerized tomography , Low density pp.553-557
Published Date 1991/6/10
DOI https://doi.org/10.11477/mf.1436900275
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Abstract

The authors report a case of dysembryoplastic neuroepithelial tumor which is a new entity of glial tumor proposed by Daumas-Duport et al. A 16-year-old male was admitted to our hospital with a 5-year history of uncontrollable complex partial seizure. CT scan showed a non-enhanced homogeneous low density area without mass effect, simulating old infarction or porencephalic cyst in the right posterior temporal lobe. The inner table of the skull over the lesion was eroded. The lesion showed low signal intensity in T1 weighted MR image and high signal intensity in T2 image. Cra-niotomy disclosed greyish soft solid tumor without cyst. Histologically, the tumor contained multiple cellular nodules in the microcystic astrocytic part which con-tained neurons. After the surgery the patient was free from the seizure.

Dysembryoplastic neuroepithelial tumor is found in young patients with intractable partial seizures. It is characterized by pseudocystic well-demarcated low den-sity appearance on CT scan. Histologically, it is an in-tracortical multinodular heterogeneous tumor which, is surgically treatable with favorable prognosis. For dif-ferential diagnosis, this tumor must be recognized in the list of low-density intracranial lesions found during CT scan.


Copyright © 1991, 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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