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多形性胶质母细胞瘤侵犯局部并破坏颅骨。病例报告及文献综述。

Local invasivity of glioblastoma multiforme with destruction of skull bone. Case report and review of the literature.

作者信息

Rainov N G, Holzhausen H J, Meyer H, Burkert W

机构信息

Department of Neurosurgery, Faculty of Medicine, Martin-Luther-University Halle, Fed. Rep. of Germany.

出版信息

Neurosurg Rev. 1996;19(3):183-8. doi: 10.1007/BF00512050.

Abstract

Primary tumors originating from cells of the glial lineage usually affect predominantly the white matter of the brain. Only rarely do gliomas destroy the surrounding bone by invasion of the extracellular matrix, especially without prior surgery. This paper describes the unusual case of a 66-year-old female patient with a left-sided intra- and extracranial tumor involving the temporal lobe, destroying the underlying skull base, and growing into the paranasal sinuses, orbit, and temporal bone. Biopsy revealed glioblastoma multiforme with strong GFAP positivity. Molecular biologic investigations of the p53, EGFR, and mdm2 genes showed functional inactivation of the p53 gene but no overexpression of oncogenes. Because the tumor was considered inoperable, palliative irradiation was carried out. The patient died 7 months after diagnosis. The causes of this phenomenon are discussed and the literature reviewed.

摘要

起源于神经胶质谱系细胞的原发性肿瘤通常主要影响脑白质。胶质瘤极少通过侵袭细胞外基质破坏周围骨骼,尤其是在未经手术的情况下。本文描述了一例罕见病例,一名66岁女性患者,左侧颞叶出现颅内和颅外肿瘤,破坏了下方的颅底,并长入鼻窦、眼眶和颞骨。活检显示多形性胶质母细胞瘤,GFAP呈强阳性。对p53、EGFR和mdm2基因的分子生物学研究表明,p53基因功能失活,但癌基因无过度表达。由于该肿瘤被认为无法手术切除,因此进行了姑息性放疗。患者在诊断后7个月死亡。本文讨论了这种现象的原因并回顾了相关文献。

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