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儿童小脑星形细胞瘤的预后

Prognosis of cerebellar astrocytomas in children.

作者信息

Villarejo Francisco, de Diego Jose Maria Belinchón, de la Riva Alvaro Gómez

机构信息

Department of Neurosurgery, Hospital Niño Jesús, C/Avda Menéndez Pelayo 65, 28009, Madrid, Spain.

出版信息

Childs Nerv Syst. 2008 Feb;24(2):203-10. doi: 10.1007/s00381-007-0449-8. Epub 2007 Aug 21.

Abstract

OBJECTIVE

Our main objective is to review a large series of cerebellar astrocytomas in children and evaluate the outcome of the patients depending on astrocytoma class. The effect of astrocytoma characteristics on the children's prognosis was determined by grouping a series of cerebellar astrocytomas by their location, radiological aspect, size, and histology and determining whether this was related with outcome.

MATERIALS AND METHODS

Two hundred and three children with cerebellar astrocytomas were retrospectively reviewed, and their tumors were classified by location, macroscopic radiological appearance, size, and histology. We have distinguished between patients operated before and after 1974 because of the introduction of new diagnostic (computed tomography, magnetic resonance) and more sophisticated treatment techniques after this year (microsurgery, laser, cavitron, etc).

RESULTS

Our patients' results were classified according to the Lapras scale/classification as normal, with some neurological deficit but able to lead a normal life, and those with severe post surgical deficits. Recurrences and mortality were also noted. Normal or good results were obtained in 111 patients, some neurological deficit in 55, and severe deficits in nine. There were six recurrences and 22 deaths because of the disease.

CONCLUSIONS

Two main factors affected prognosis. One was whether the tumor was completely resected or not; this was the treatment in most cases in this series. The second factor was the location, size, and macroscopic appearance of the tumor. The best prognosis was associated with being located in one hemisphere, being cystic, being cystic with a posterior nodule, and/or being small.

摘要

目的

我们的主要目的是回顾一大组儿童小脑星形细胞瘤病例,并根据星形细胞瘤的类型评估患者的预后。通过将一系列小脑星形细胞瘤按其位置、影像学表现、大小和组织学进行分组,并确定这是否与预后相关,来确定星形细胞瘤特征对儿童预后的影响。

材料与方法

对203例患有小脑星形细胞瘤的儿童进行回顾性研究,并根据其位置、宏观影像学表现、大小和组织学对肿瘤进行分类。由于1974年之后引入了新的诊断方法(计算机断层扫描、磁共振成像)以及更先进的治疗技术(显微手术、激光、超声吸引等),我们区分了1974年之前和之后接受手术的患者。

结果

我们根据拉普拉斯量表/分类法将患者的结果分为正常、有一些神经功能缺损但能够正常生活以及术后有严重缺损三类。还记录了复发和死亡情况。111例患者获得正常或良好结果,55例有一些神经功能缺损。

结论

有两个主要因素影响预后。一个因素是肿瘤是否完全切除;在本系列的大多数病例中这是主要的治疗方式。另一个因素是肿瘤的位置、大小和宏观外观。最佳预后与位于一个半球、呈囊性、有后结节的囊性以及/或者体积小有关。

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