Kepes J J, Rubinstein L J
Cancer. 1981 May 15;47(10):2451-9. doi: 10.1002/1097-0142(19810515)47:10<2451::aid-cncr2820471024>3.0.co;2-5.
Three cases of heavily lipidized malignant glioma are reported. Large amounts of intracellular lipid gave the tumor cells a vacuolated, foamy appearance that generally obscured their glial nature. The latter was, however, confirmed by the demonstration of glial fibrillary acidic protein (GFAP) by immunoperoxidase. These tumors, which were situated deeply in the brain and contained areas of necrosis, must be distinguished from the relatively benign pleomorphic meningocerebral xanthoastrocytomas, which are characteristically superficial in their location and lack necrotic foci. The malignant nature of the presently described tumors is shown by the death of all three patients within one year of surgery. Thus, in the biologic sense these tumors represent glioblastomas; however, their morphologic peculiarities in the form of massive lipidization of tumor cells, apparently not caused by necrobiosis, set them aside as a histologic subgroup.
本文报告了3例高度脂质化的恶性胶质瘤。大量细胞内脂质使肿瘤细胞呈现空泡状、泡沫样外观,通常掩盖了其胶质细胞特性。然而,通过免疫过氧化物酶法检测胶质纤维酸性蛋白(GFAP)证实了其胶质细胞特性。这些肿瘤位于脑深部,含有坏死区域,必须与相对良性的多形性脑膜脑黄瘤星形细胞瘤相鉴别,后者的特征是位于浅表且缺乏坏死灶。目前描述的这些肿瘤的恶性本质表现为所有3例患者均在手术后1年内死亡。因此,从生物学意义上讲,这些肿瘤代表胶质母细胞瘤;然而,其肿瘤细胞大量脂质化的形态学特征显然并非由渐进性坏死所致,使其成为一个组织学亚组。