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九例中脑胶质瘤的临床病理研究

[A clinicopathological study of nine cases of midbrain glioma].

作者信息

Nitta T, Sato K

机构信息

Department of Neurosurgery, Juntendo University School of Medicine, Tokyo.

出版信息

No Shinkei Geka. 1995 May;23(5):405-10.

PMID:7753319
Abstract

The majority of brain stem gliomas tend to occur during childhood and arise in the pons. The prognosis of these typical pontine gliomas is almost invariably bad. In contrast, there exists a group of benign brain stem gliomas, mostly arising from the midbrain and are amenable to surgical resection. They are often low-grade astrocytomas and are associated with better prognosis. We summarized nine cases of intrinsic midbrain gliomas and their clinical behavior was analyzed by radioimagings and histopathological examination. They were classified from CT images according to Stroink et al. and from anatomic staging by Epstein. The result showed that 5 in 9 cases were so called, "focal midbrain gliomas". That is to say, the tumor arose from the tectal plate or the tegmentum of the mesencephalon and expanded dorsally, but did not invade the surrounding neural tissues. Three focal midbrain gliomas in childhood were well demarcated and surgically resectable. Histologically, tumors were astrocytomas and were associated with favorable prognosis. However, two focal midbrain gliomas in adulthood were anaplastic astrocytoma and the prognosis was poor, even though they appeared similar shown on radioimaging study. The overall survival rate of patients with midbrain glioma was longer than that of patients with glioma in the cerebral hemisphere. From these results, it was concluded that a specific group of intrinsic, focal midbrain gliomas can be classified into pediatric benign gliomas and adolescent malignant ones. A further number of cases should be studied to clarify this hypothesis.

摘要

大多数脑干胶质瘤倾向于在儿童期发生,且起源于脑桥。这些典型的脑桥胶质瘤的预后几乎总是很差。相比之下,存在一组良性脑干胶质瘤,大多起源于中脑,适合手术切除。它们通常是低级别星形细胞瘤,预后较好。我们总结了9例中脑原发性胶质瘤,并通过影像学和组织病理学检查分析了它们的临床行为。根据Stroink等人的方法从CT图像进行分类,并根据Epstein的方法进行解剖分期。结果显示,9例中有5例为所谓的“局灶性中脑胶质瘤”。也就是说,肿瘤起源于中脑顶盖或被盖,并向背侧扩展,但未侵犯周围神经组织。3例儿童期的局灶性中脑胶质瘤界限清楚,可手术切除。组织学上,肿瘤为星形细胞瘤,预后良好。然而,2例成年期的局灶性中脑胶质瘤为间变性星形细胞瘤,尽管在影像学研究中表现相似,但预后较差。中脑胶质瘤患者的总体生存率高于大脑半球胶质瘤患者。从这些结果可以得出结论,一组特定类型内生性、局灶性中脑胶质瘤可分为儿童良性胶质瘤和青少年恶性胶质瘤。需要进一步研究更多病例以阐明这一假说。

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