Friede R L, Janzer R C, Roessmann U
Acta Neuropathol. 1982;57(2-3):103-10. doi: 10.1007/BF00685377.
Fourteen juvenile patients with small cell gliomas were studied at two institutes. These tumors are believed to form a distinct entity. They arise mostly in the diencephalon or the brain stem and are composed of a poorly differentiated small cell component having a pronounced tendency to differentiate into a glioma. Signs of neuroblastic differentiation were also found with the electron microscope. Small cell gliomas disseminate early and profusely throughout the ventricular walls and the subarachnoid spaces including the spinal meninges. Prognosis is grave, most patients dying within 1 year of diagnosis or surgical intervention. The designation "infantile small cell glioma" overlaps with both the "metastasising gliomas in young subjects" of Eade and Urich (1971) and with the primitive neuroectodermal tumor of infancy of Hart and Earle (1973).
在两家机构对14例患有小细胞胶质瘤的青少年患者进行了研究。这些肿瘤被认为构成一个独特的实体。它们大多起源于间脑或脑干,由分化不良的小细胞成分组成,具有明显的向胶质瘤分化的倾向。电子显微镜检查也发现了神经母细胞分化的迹象。小细胞胶质瘤早期广泛播散至脑室壁和蛛网膜下腔,包括脊髓脑膜。预后严重,大多数患者在诊断或手术干预后1年内死亡。“婴儿小细胞胶质瘤”这一命名与伊德和乌里奇(1971年)的“年轻受试者转移性胶质瘤”以及哈特和厄尔(1973年)的婴儿原始神经外胚层肿瘤都有重叠。