Daumas-Duport C, Varlet P, Tucker M L, Beuvon F, Cervera P, Chodkiewicz J P
Department of Pathology-Neurooncology, Hôpital Sainte-Anne, Paris, France.
J Neurooncol. 1997 Aug;34(1):37-59. doi: 10.1023/a:1005707203596.
The present study has attempted to demonstrate that the morphological spectrum of oligodendrogliomas includes tumors which are traditionally misinterpreted as 'diffuse fibrillary astrocytoma'. We have shown that these tumors are in fact made of isolated neoplastic oligodendrocytes which are entrapped in a fibrillary background composed of axons and fibrillary reactive gliosis. Analysis in a series of 153 'pure' supratentorial oligodendrogliomas composed of 'classical' or pseudo 'diffuse fibrillary oligodendrogliomas' diagnosed by imaging-based serial stereotactic biopsies showed that 2/3 of the tumors were exclusively made of isolated tumor cells (ITCs) (structure type III) and that only 1/3 of them exhibited both ITCs and solid tumor tissue components (structure type II). The tumor tissue destroys the brain parenchyma and contains new formed microblood vessels whereas ITCs do not destroy the parenchyma and are not associated with microangiogenesis. These fundamentally opposite morphological characteristics were reflected by the following findings: 1) contrast enhancement was observed in 64% of structure type II but was never seen in structure type III oligodendrogliomas. 2) a neurological deficit occurred in 57% of structure type II but in only 8% of structure type III oligodendrogliomas. 3) using the new grading system described in the companion paper to this study, we found that the biological behavior of oligodendrogliomas was also closely related to the patterns of tumor growth. From a synthesis of data gathered in this study it is suggested that emergence of microangiogenesis within a tumor which at first grows slowly with a structure type III pattern is a crucial event toward more aggressive behavior.
本研究试图证明少突胶质细胞瘤的形态学谱包括一些传统上被误诊为“弥漫性纤维性星形细胞瘤”的肿瘤。我们已经表明,这些肿瘤实际上是由孤立的肿瘤性少突胶质细胞组成,这些细胞被困在由轴突和纤维性反应性胶质增生构成的纤维性背景中。对一系列153例“纯”幕上少突胶质细胞瘤进行分析,这些肿瘤由基于影像学的系列立体定向活检诊断为“经典”或假性“弥漫性纤维性少突胶质细胞瘤”,结果显示,2/3的肿瘤仅由孤立肿瘤细胞(ITCs)组成(结构类型III),只有1/3的肿瘤同时具有ITCs和实体肿瘤组织成分(结构类型II)。肿瘤组织破坏脑实质并含有新生微血管,而ITCs不破坏实质且与微血管生成无关。这些根本相反的形态学特征反映在以下发现中:1)64%的结构类型II出现对比增强,但在结构类型III少突胶质细胞瘤中从未观察到。2)57%的结构类型II出现神经功能缺损,而在结构类型III少突胶质细胞瘤中仅为8%。3)使用本研究配套论文中描述的新分级系统,我们发现少突胶质细胞瘤的生物学行为也与肿瘤生长模式密切相关。综合本研究收集的数据表明,起初以结构类型III模式缓慢生长的肿瘤内微血管生成的出现是向更具侵袭性的行为发展的关键事件。