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[脑胶质母细胞瘤的继发性定位。关于一例因椎体受累而发现多发骨转移病例的致病及解剖临床重点]

[Secondary localizations of cerebral glioblastoma. Pathogenic and anatomoclinical focus apropos of a case of multiple bone metastases disclosed by vertebral involvement].

作者信息

Malca S A, Roche P H, Pellet W

机构信息

Service de Neurochirurgie, Hôpital Sainte-Marguerite (Pr A. Combalbert, Marseille.

出版信息

Neurochirurgie. 1993;39(5):315-21.

PMID:8065490
Abstract

This report describes a case of a cerebral glioblastoma with multiple metastases appeared two years after craniotomy and revealed by a diffuse vertebral involvement with a lumbo-sciatic pain. The experimental and clinical data from the literature about distant localizations of glioblastoma give the arguments for the rarity and the pathogenic modes of the natural course. The distant localizations of cerebral glioblastoma, identified by immunohistochemical staining for glial fibrillary acidic protein, occurred in young patients, late in the follow-up which the duration is longer than those of classical glioblastomas; their occurrence hasten the disease course. Two distinct oncological entities might be identified: metastases, using blood or lymphatic pathways, commonly from a supra-tentorial primary tumor, are facilitated by surgical treatment; their exclusive extraneural sites are usually symptomatic; grafts, by seeding via cerebrospinal fluid pathways, are spontaneous or facilitated by tumoral removal and are disseminated along the neuraxis; they occur frequently and are usually asymptomatic; when shunts induce them, it gives rise to symptomatic peritoneal seeding; they seem to concern poor invading primary glioblastomas. The extraneural (metastasis) or neuraxial (graft) sites and the ways of occurrence (spontaneous, or facilitated by craniotomy or induced by surgical shunts) allow to classify the distant localizations of glioblastoma in six pathogenic types.

摘要

本报告描述了一例脑胶质母细胞瘤病例,该病例在开颅术后两年出现多处转移,并表现为弥漫性椎体受累及腰腿痛。文献中关于胶质母细胞瘤远处定位的实验和临床数据为其自然病程的罕见性和致病模式提供了依据。通过胶质纤维酸性蛋白免疫组化染色确定的脑胶质母细胞瘤远处定位发生在年轻患者中,随访后期出现,其持续时间比经典胶质母细胞瘤更长;它们的出现加速了病程。可能识别出两种不同的肿瘤实体:转移灶,通常通过血液或淋巴途径,多源于幕上原发性肿瘤,手术治疗会促使其发生;其唯一的神经外部位通常有症状;种植灶,通过脑脊液途径播散,可为自发或因肿瘤切除而促成,沿神经轴扩散;它们经常发生且通常无症状;当分流术诱发种植灶时,会导致有症状的腹膜种植;它们似乎与侵袭性较弱的原发性胶质母细胞瘤有关。神经外(转移)或神经轴(种植)部位以及发生方式(自发、开颅手术促成或手术分流诱发)可将胶质母细胞瘤的远处定位分为六种致病类型。

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