Heyerdahl Strøm E, Skullerud K
Clin Neuropathol. 1983;2(4):188-91.
Five cases of pleomorphic xanthoastrocytoma are described. The favorable prognosis of these tumors is confirmed. Thus, two patients had postoperative survival of 9 and 12 years, respectively, and three others are still alive and well, one of them 6 years after the operation. All the cases described until now (17 including the ones described here) have involved patients under 30 years of age. Most of the tumors have been located superficially in the brain with extensive adhesions to the meninges. Usually they have been well demarcated from the brain. Histologically, the tumors showed a marked cellular pleomorphism, including bizarre giant cells, but there were few mitoses and only a slight tendency to necrosis. The tumor tissue contained a dense network of reticulin fibers and many cells contained lipid vacuoles. Glial fibrillary acidic protein (GFAP) was demonstrated in the cytoplasm of the tumor cells.
本文描述了5例多形性黄色星形细胞瘤。这些肿瘤预后良好得到了证实。因此,两名患者术后分别存活了9年和12年,另外三名患者仍然健在,其中一名患者术后已6年。到目前为止所描述的所有病例(包括本文所述的病例共17例)均为30岁以下的患者。大多数肿瘤位于脑浅表部位,与脑膜有广泛粘连。通常它们与脑分界清楚。组织学上,肿瘤表现出明显的细胞多形性,包括怪异的巨细胞,但有丝分裂少见,仅有轻微的坏死倾向。肿瘤组织含有致密的网状纤维网络,许多细胞含有脂质空泡。肿瘤细胞的细胞质中显示有胶质纤维酸性蛋白(GFAP)。