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右侧颞叶胶质母细胞瘤累及左侧眼眶。病例报告。

Right temporal lobe glioblastoma presenting in the left orbit. Case report.

作者信息

Kros J M, van den Berge H, Tanghe H L, Bakker S L

机构信息

Department of Pathology, University Hospital Rotterdam, The Netherlands.

出版信息

J Neurosurg. 2000 Apr;92(4):702-5. doi: 10.3171/jns.2000.92.4.0702.

DOI:10.3171/jns.2000.92.4.0702
PMID:10761663
Abstract

Dissemination of gliomas outside the central nervous system without preceding neurosurgery is a rare phenomenon. Glial neoplasms presenting as bone lesions are even more rare. A case of glioblastoma multiforme (GBM) with initial presentation in the orbit following a single generalized seizure is described. Signs of intracranial hypertension resulted from subarachnoid tumor invasion. The patient was treated with whole-dose radiation therapy but survived for only 6 months following the initial presentation. An autopsy revealed a right temporal GBM with extensive subarachnoid spread and invasion in the left orbit and skull base. The literature on dissemination of primary tumors of the brain is reviewed.

摘要

胶质瘤在没有先前神经外科手术的情况下扩散至中枢神经系统外是一种罕见现象。以骨病变形式出现的胶质肿瘤更为罕见。本文描述了一例多形性胶质母细胞瘤(GBM),首发表现为单次全身性癫痫发作后眼眶病变。蛛网膜下腔肿瘤侵犯导致颅内高压症状。患者接受了全剂量放射治疗,但首发后仅存活6个月。尸检显示右颞叶GBM,伴有广泛的蛛网膜下腔扩散并侵犯左眼眶和颅底。本文对原发性脑肿瘤扩散的相关文献进行了综述。

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引用本文的文献

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Primary bone destruction and extracranial metastases in an atypical glioblastoma with sarcomatoid features.具有肉瘤样特征的非典型性胶质母细胞瘤中的原发性骨破坏和颅外转移。
BMJ Case Rep. 2022 Aug 18;15(8):e247248. doi: 10.1136/bcr-2021-247248.
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Multicystic oligodendroglioma with calvarial destruction.伴有颅骨破坏的多囊性少突胶质细胞瘤。
Asian J Neurosurg. 2014 Apr;9(2):93-5. doi: 10.4103/1793-5482.136723.
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Glioblastoma multiforme causing calvarial destruction: an unusual manifestation revisited.多形性胶质母细胞瘤导致颅骨破坏:对一种不寻常表现的重新审视。
AJNR Am J Neuroradiol. 2004 Oct;25(9):1533-7.