Guo L X, Zhang R L
Panzhihua Central Hospital, Sichuan Province.
Zhonghua Zhong Liu Za Zhi. 1990 Nov;12(6):477-8.
Pleomorphic xanthoastrocytoma (PXA) is a very rare and special kind of astrocytoma. Most of the patients have a relatively favorable prognosis despite its bizarre and pleomorphic cells. A 13 year old girl with PXA in the right occipitoparietal region is reported. Under light microscope, the tumor was markedly pleomorphic; mitosis was occasionally encountered and necrosis was absent. Immunohistochemically, cytoplasm of the tumor cells was positive for GFAP stain. Under electron microscope, many tumor cells contained glial filaments and large lipid vacuoles. Pericellular basal laminae could be found about some tumor cells, indicating a possible origin from subpial astrocyte. The clinicopathologic features, histogenesis, differential diagnosis and prognosis of PXA are discussed with review of literature.
多形性黄色星形细胞瘤(PXA)是一种非常罕见且特殊的星形细胞瘤。尽管其细胞怪异且具有多形性,但大多数患者的预后相对良好。本文报道了一名13岁右枕顶部患有PXA的女孩。光镜下,肿瘤具有明显的多形性;偶见有丝分裂,无坏死。免疫组化显示,肿瘤细胞的胞质GFAP染色呈阳性。电镜下,许多肿瘤细胞含有胶质细丝和大的脂质空泡。部分肿瘤细胞周围可见细胞周基膜,提示可能起源于软脑膜下星形胶质细胞。结合文献复习,对PXA的临床病理特征、组织发生、鉴别诊断及预后进行了讨论。