Shepherd C W, Scheithauer B W, Gomez M R, Altermatt H J, Katzmann J A
Department of Neurology, Mayo Clinic, Rochester, Minnesota.
Neurosurgery. 1991 Jun;28(6):864-8.
Of 345 patients with tuberous sclerosis complex evaluated at the Mayo Clinic from 1950 to 1989, 23 were identified as having brain tumors. In 20 of the 23, histological or clinical evidence showed the tumor to be a subependymal giant cell astrocytoma. A search of the Mayo Clinic tissue registry yielded 73 giant cell-containing astrocytomas and intraventricular gliomas exclusive of ependymomas. Reexamination revealed no further examples of subependymal giant cell astrocytoma in patients without features of the tuberous sclerosis complex. Considerable histological variation was observed in the 15 subependymal giant cell astrocytomas subjected to critical microscopic review. It is of note that no correlation was noted between either the histological features, such as atypia, mitoses, endothelial proliferations, necrosis, or the flow cytometric characteristics and the clinical course or the survival time of the patients.
1950年至1989年在梅奥诊所接受评估的345例结节性硬化症患者中,有23例被确诊患有脑肿瘤。在这23例患者中,有20例的组织学或临床证据显示肿瘤为室管膜下巨细胞星形细胞瘤。对梅奥诊所组织登记处进行检索,得到了73例含巨细胞的星形细胞瘤和脑室内胶质瘤,但不包括室管膜瘤。重新检查发现,在没有结节性硬化症特征的患者中,没有发现更多室管膜下巨细胞星形细胞瘤的病例。对15例接受严格显微镜检查的室管膜下巨细胞星形细胞瘤进行观察,发现其组织学差异很大。值得注意的是,无论是组织学特征,如异型性、有丝分裂、内皮细胞增殖、坏死,还是流式细胞术特征,均与患者的临床病程或生存时间无关。