【CCT中多形性胶质母细胞瘤如钙质沉着症的异常病程】。

S Victor, Y Altay, T Schneider
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引用次数: 1

摘要

我们报告一例罕见的多灶双半球胶质母细胞瘤(WHO IV级),其异常的过程:在通过开放活检和右顶叶至头叶次全肿瘤切除术的组织学诊断时,肿瘤病变表现为9个月不变的轻微钙化,然后在CCT中发展为多眼双半球高密度-低密度区域,边缘对比增强,1个月内局部水肿。本文讨论了这一特殊病例的肿瘤组织发生,并将胚胎发生概念与肿瘤分级概念进行了对比。从临床相关性来看,即使CCT长时间不变的单灶钙化也可能是胶质母细胞瘤发生的第一个征兆,因此短期的临床和计算机断层扫描控制是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Unusual course of glioblastoma multiforme as calcinosis in CCT].

We report about a rare case of multifocal bihemispheric glioblastoma (WHO grade IV) with unusual course: At time of histological diagnosis via open biopsy and subtotal tumor resection right parieto-occipital the tumorous lesion presents itself for nine months unchanged as a little calcification right parietal, before developing in CCT multiocular bihemispheric hyperdens-hypodens areals with margin contrast enhancement and perifocal edema within one month. Tumor histogenesis of this special case is discussed contrasting the embryogenetic concept with the concept of tumor-grading. From clinical relevance is the fact that even a long time unchanged unifocal calcification in CCT could be the first sign of developing glioblastoma, and so short-term clinical and computer tomographic controls are necessary.

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