Kros J M, Vecht C J, Stefanko S Z
Department of Pathology/Neuropathology, Academic Hospital Rotterdam-Dijkzigt, The Netherlands.
Hum Pathol. 1991 Nov;22(11):1128-35. doi: 10.1016/0046-8177(91)90265-q.
Five brain tumors with the histopathologic features of pleomorphic xanthoastrocytomas (PXAs) are presented. Computed tomography scans showed a remarkable homology. Two cases had atypical localizations for a PXA, while one 46-year-old patient did not conform to the normal age distribution of this tumor. Nevertheless, in these cases, the histopathology was always characteristic for PXA, a remarkable pleomorphism, in addition to simultaneous expression of glial fibrillary acidic protein and histiocytic markers in the various tumor cells. In one of the presented tumors, however, clusters of neoplastic neuronal cells were also found. In this particular case, differential diagnostic criteria to distinguish between a PXA and a desmoplastic infantile ganglioglioma are lacking.
本文报告了5例具有多形性黄色星形细胞瘤(PXA)组织病理学特征的脑肿瘤。计算机断层扫描显示出显著的相似性。2例PXA具有非典型定位,而1例46岁患者不符合该肿瘤的正常年龄分布。然而,在这些病例中,组织病理学始终具有PXA的特征,即显著的多形性,此外各种肿瘤细胞中同时表达胶质纤维酸性蛋白和组织细胞标志物。然而,在所呈现的肿瘤之一中,还发现了肿瘤性神经元细胞簇。在这种特殊情况下,缺乏区分PXA和促纤维增生性婴儿型神经节胶质瘤的鉴别诊断标准。