Herpers M J, Budka H
Acta Neuropathol. 1984;64(4):265-72. doi: 10.1007/BF00690392.
Immuno-reactivity to glial fibrillary acidic protein (GFAP) is mainly regarded as a sign of astroglial histogenesis and/or differentiation. The presence of astrocytes in oligodendrogliomas is a well known phenomenon; in addition, GFAP-positive neoplastic oligodendrocytes have also been described but have not yet been studied systematically. Using an anti-GFAP serum in the peroxidase-antiperoxidase antiperoxidase (PAP) technique, 50 oligodendrogliomas and 16 mixed oligodendrocytomas were investigated; they had been diagnosed by routine histological stains. In half of all oligodendrogliomas, and only in a few (12%) of the mixed oligoastrocytomas, GFAP-positive oligodendrocytes were found in some areas of the classical honey-comb texture with a prominent vascular stroma. The term 'gliofibrillary oligodendrocyte' (gfoc) is proposed for these immuno-reactive cells. The existence of a tumour cell combining morphological characteristics of oligodendroglia with GFAP production in its cytoplasm may be considered analogous to transient GFAP expression by myelin-forming glia during normal development (Choi and Kim 1984), thus suggesting the return to a foetal behaviour by some neoplastic oligodendrocytes. Three tumours of the present series consisted largely of gfocs and, therefore, may be termed gliofibrillary oligodendrogliomas. In about 32% of all oligodendrogliomas, but only once in the mixed tumour group, a gradual morphological transition from gfocs to gemistocytic astrocytes was observed.(ABSTRACT TRUNCATED AT 250 WORDS)
对胶质纤维酸性蛋白(GFAP)的免疫反应性主要被视为星形胶质细胞组织发生和/或分化的标志。少突胶质细胞瘤中存在星形胶质细胞是一个众所周知的现象;此外,也有关于GFAP阳性的肿瘤性少突胶质细胞的描述,但尚未进行系统研究。使用抗GFAP血清,采用过氧化物酶-抗过氧化物酶(PAP)技术,对50例少突胶质细胞瘤和16例混合性少突胶质细胞瘤进行了研究;这些病例均经常规组织学染色确诊。在所有少突胶质细胞瘤的一半病例中,且仅在少数(12%)混合性少突星形细胞瘤中,在具有显著血管间质的典型蜂窝状结构区域发现了GFAP阳性的少突胶质细胞。对于这些免疫反应性细胞,提出了“胶质纤维性少突胶质细胞”(gfoc)这一术语。肿瘤细胞在细胞质中结合少突胶质细胞的形态特征并产生GFAP,这一现象可能类似于正常发育过程中形成髓鞘的胶质细胞短暂表达GFAP(Choi和Kim,1984年),因此提示一些肿瘤性少突胶质细胞恢复到胎儿期行为。本系列中的三个肿瘤主要由gfoc组成,因此可称为胶质纤维性少突胶质细胞瘤。在所有少突胶质细胞瘤中约32%的病例中观察到从gfoc到肥胖型星形胶质细胞的逐渐形态转变,但在混合性肿瘤组中仅观察到一次。(摘要截短于250字)