Aebi M, Kraus-Ruppert R
J Neurol. 1978 Oct 25;219(2):139-44. doi: 10.1007/BF00314397.
Clinico-pathologic report of a patient with an oligodendroglioma who ran a 22-year course characterized by focal epileptic seizures of the Jaksonian type. The EEG remained normal for many years. Since the tumor had not been influenced by therapeutic measures, the histologic picture permitted considering some basic problems of origin, growth, and differentiation of oligodendrogliomas.
一名少突胶质细胞瘤患者的临床病理报告,该患者病程长达22年,以杰克逊型局灶性癫痫发作为特征。脑电图多年来一直正常。由于肿瘤未受治疗措施影响,组织学表现有助于思考少突胶质细胞瘤起源、生长和分化的一些基本问题。