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[小脑恶性星形细胞瘤。附10例报告并文献复习]

[Malignant astrocytoma of the cerebellum. Apropos of 10 cases. Review of the literature].

作者信息

Rizk T, Remond J, Alhayek G, Fournier D, Menei P, Mercier P, Guy G

机构信息

Service de Neurochirurgie, Centre Hospitalier et Universitaire, Angers.

出版信息

Neurochirurgie. 1994;40(2):121-6.

PMID:7870245
Abstract

While reviewing a series of 138 cerebellar tumors operated upon between 1978 and 1991, the authors could only find 2 glioblastomas and 8 anaplastic astrocytomas, occurring in 4 children (3 to 14 years old) and 6 adults (23 to 48 years old). These 10 cases represent 2% of the all malignant gliomas population observed during the same period of time. Clinically speaking, nothing makes these tumors different from other cerebellar ones. However, with an heterogenous image and an irregular contrast enhancement, the CT (scan) appearance can lead to the diagnosis. 7 lesions develop within the cerebellar vermis (vermis cerebelli) and 3 develop within the cerebellar hemisphere. Total surgical resection is performed in 9 cases and subtotal resection in 1 case (because of the extension to the floor of the fourth ventricle). Adjunctive radiotherapy on their posterior cranial fossa is achieved in 8 cases. The 2 patients with a glioblastoma present with a recurrence of their tumor at 15 months and 6 years respectively, and eventually died. Out of the patients with an anaplastic astrocytoma, 4 are still alive without recurrence and with a median follow-up of 7 years. The pathogenesis of such lesions is discussed. An aggressive therapeutic management is suggested because of the possible prolonged survival rate.

摘要

在回顾1978年至1991年间接受手术的138例小脑肿瘤时,作者仅发现2例胶质母细胞瘤和8例间变性星形细胞瘤,发生于4名儿童(3至14岁)和6名成人(23至48岁)。这10例病例占同期观察到的所有恶性胶质瘤患者的2%。从临床角度来看,这些肿瘤与其他小脑肿瘤并无差异。然而,CT(扫描)表现为图像异质性和不规则对比增强,可据此做出诊断。7个病灶发生在小脑蚓部,3个病灶发生在小脑半球。9例患者进行了全切除,1例因肿瘤延伸至第四脑室底部进行了次全切除。8例患者接受了后颅窝辅助放疗。2例胶质母细胞瘤患者分别在15个月和6年后肿瘤复发,最终死亡。在间变性星形细胞瘤患者中,4例仍然存活且无复发,中位随访时间为7年。本文讨论了此类病变的发病机制。鉴于可能延长生存率,建议采取积极的治疗措施。

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