Cervoni L, Salvati M, Santoro A, Celli P
Department of Neurological Sciences, 1 Chair of Neurosurgery, La Sapienza, University of Rome, Italy.
Neurosurg Rev. 1996;19(1):13-6. doi: 10.1007/BF00346603.
The authors describe 3 cases of cerebral pleomorphic xanthoastrocytoma, one of which has an unusual neuroradiological appearance, and review the clinical and prognostic features of the 96 cases reported in the literature. Pleomorphic xanthoastrocytoma is a neuroectodermal tumor that affects young patients, in a superficial or supratentorial site, most frequently at the temporal level. It is difficult to formulate a differential diagnosis with other neuroectodermal tumors or with meningioma on the basis et neuroradiological appearance, as demonstrated by one of the cases reported here. The prognosis of this tumor is very good, regardless of the type of treatment performed, although both relapse and, more rarely, malignant tumor evolution are possible.
作者描述了3例脑多形性黄色星形细胞瘤,其中1例具有不寻常的神经放射学表现,并回顾了文献报道的96例病例的临床和预后特征。多形性黄色星形细胞瘤是一种神经外胚层肿瘤,多见于年轻患者,位于浅表或幕上部位,最常见于颞叶。正如本文报道的其中1例病例所示,基于神经放射学表现很难与其他神经外胚层肿瘤或脑膜瘤进行鉴别诊断。尽管可能出现复发,更罕见的是出现恶性肿瘤进展,但无论采用何种治疗方式,该肿瘤的预后都非常好。