Bayindir C, Balak N, Karasu A, Kasaroğlu D
Department of Neurosurgery, University of Istanbul, School of Medicine, Turkey.
Childs Nerv Syst. 1997 Jan;13(1):50-6. doi: 10.1007/s003810050040.
A case of anaplastic pleomorphic xanthoastrocytoma (PXA) in a 9-year-old girl is reported. Histological features of PXAs are cellular pleomorphism of GFAP-positive cells, with intracytoplasmic lipidic vacuoles and a reticulin network, bizarre giant cells, low mitotic activity, and lack of necrosis and of endothelial vascular proliferations. These tumors are generally reported to have a favorable postoperative course. In our case, a poor clinical prognosis and spread of the illness through the CSF was observed. Immunohistochemical features of the tumor, which were histologically anaplastic in nature, were analyzed. There were small foci of necrosis in the sections of the material obtained at the first operation and extensive necrosis in that from the second operation, although the patient had not received radiotherapy between the operations. The presence of necrosis in PXA is an uncommon and significant feature. It predicts the poor prognosis seen in this case, and therefore this report strongly supports the notion that necrosis should automatically exclude a tumor from the PXA category. The histological grade was evaluated as grade 3 (according to the WHO classification).
报道了一例9岁女孩的间变性多形性黄色星形细胞瘤(PXA)。PXA的组织学特征为GFAP阳性细胞的细胞多形性,伴有胞浆内脂质空泡和网状纤维网络、怪异的巨细胞、低有丝分裂活性,且无坏死和内皮血管增生。这些肿瘤通常报道术后病程良好。在我们的病例中,观察到临床预后不良且疾病通过脑脊液扩散。对该肿瘤的免疫组织化学特征进行了分析,其在组织学上本质为间变性。首次手术获取的材料切片中有小灶性坏死,第二次手术的材料中有广泛坏死,尽管患者在两次手术之间未接受放疗。PXA中出现坏死是一种罕见且重要的特征。它预示了该病例中所见的不良预后,因此本报告有力支持了坏死应自动将肿瘤排除在PXA类别之外的观点。组织学分级评估为3级(根据世界卫生组织分类)。