首页> 美国卫生研究院文献>Neuro-Oncology >O8.07HISTOLOGY LOCALISATION TREATMENT AND OUTCOME OF 339 CONSECUTIVE CHILDREN AND ADOLESCENTS WITH LOW GRADE GLIOMAS TREATED AT THE MEDICAL UNIVERSITY OF VIENNA BETWEEN 1993 AND 2012
【2h】

O8.07HISTOLOGY LOCALISATION TREATMENT AND OUTCOME OF 339 CONSECUTIVE CHILDREN AND ADOLESCENTS WITH LOW GRADE GLIOMAS TREATED AT THE MEDICAL UNIVERSITY OF VIENNA BETWEEN 1993 AND 2012

机译:O8.07维也纳医科大学对339名低分级胶质瘤的连续性中小学生和青少年的组织学定位治疗和结果

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Low grade gliomas (LGG) comprise a spectrum of different tumor entities corresponding to WHO grade I and II, including pilocytic astrocytoma, diffuse glioma and glioneuronal tumors. LGG in children differ in histologic distribution, molecular profile, localisation in the CNS and outcome from LGGs in adults. We report on a series of patients treated at a single center over 20 years. PATIENTS: Between 1993 and 2012, 339 consecutive patients with a median age of 8 years (range 4 months - 18 years, p25 = 3.7 years, p75 = 13.4 years) were treated at the Medical University of Vienna. 19.5% of the patients were <3 years of age at diagnosis. Gender distribution was equal. Tumors were associated with syndromes in 84 of the patients (NF1: n = 64, TSC: n = 17, and other: n = 3). Localisation was supratentorial midline in 112, cerebral hemispheres in 105, posterior fossa in 86, ventricular system in 27 and spinal in 9 patients. 66 patients with a median age of 4.4 years had optic pathway gliomas. RESULTS: Gross total resection was performed in 109, subtotal resection in 49, partial resection in 57, and biopsy in 22 patients. 83 patients had no surgery (patients with NF1, TSC, tectal glioma or tumors confined to the optic nerves and chiasm), and in the remaining the degree of resection was not evaluable. 37 patients had 2 tumor surgeries, 14 three, 5 four and one had 5 tumor surgeries during their course of disease. Histology was pilocytic astrocytoma in 122, pilomyxoid astrocytoma in 10, diffuse astrocytoma in 42, ganglioglioma in 30, subependymal giant cell astrocytoma in 17, oligoastrocytoma in 11, and other rarer histologies in the remaining patients. Twelve patients (3.5%) died and 84 patients (24.8%) had at least one event. After a median follow-up of 107 months (14-300) the 1-year overall survival (OS) was 100%, the 10-year OS 96.1 ± 1.2%, and the 20-year OS 95.3 ± 1.4%. Event-free survival (EFS) after 1 year was 92.9 ± 1.4%, after 10 years 73.8 ± 2.6% and after 20 years 67.9 ± 3.4%. CONCLUSION: While long term survival of children and adolescents with low grade gliomas is better than of adults, recurrence and death may occur even in WHO grade I tumors and regular surveillance MRI is recommended.
机译:低度神经胶质瘤(LGG)包括一系列对应于WHO I和II级的不同肿瘤实体,包括毛细胞星形细胞瘤,弥漫性神经胶质瘤和神经胶质瘤。儿童的LGG在组织学分布,分子特征,中枢神经系统中的定位以及成人LGG的结局方面存在差异。我们报告了在一个中心接受治疗超过20年的一系列患者。患者:1993年至2012年,维也纳医科大学治疗了339位中位年龄为8岁(范围为4个月至18岁,p25 = 3.7岁,p75 = 13.4岁)的连续患者。 19.5%的患者在诊断时小于3岁。性别分布相等。 84名患者的肿瘤与综合征相关(NF1:n = 64,TSC:n = 17,其他:n = 3)。定位在幕上中线112例,脑半球105例,后颅窝86例,心室系统27例,脊柱9例。 66名中位年龄为4.4岁的患者患有视神经胶质瘤。结果:109例行全切除术,49例行次全切除术,57例行部分切除术,22例行活检。 83例患者不做任何手术(患有NF1,TSC,顶神经胶质瘤或局限在视神经和棘突的肿瘤)的患者,其余的切除程度无法评估。 37名患者进行了2次肿瘤手术,其中14次进行了3次,5次4次,其中1次进行了5次肿瘤手术。组织学上有绒毛样星形细胞瘤122例,绒毛样星形细胞瘤10例,弥漫性星形细胞瘤42例,神经胶质瘤30例,室管膜下巨细胞星形细胞瘤17例,少星形胶质细胞瘤11例。有12名患者(3.5%)死亡,并且84名患者(24.8%)发生了至少一次事件。经过107个月的中位随访(14-300),一年的总生存率(OS)为100%,十年的OS为96.1±1.2%,而20年的OS为95.3±1.4%。一年后的无事件生存(EFS)为92.9±1.4%,十年后为73.8±2.6%,而20年后为67.9±3.4%。结论:尽管低级神经胶质瘤的儿童和青少年的长期生存优于成人,但即使在WHO WHO I级肿瘤中也可能发生复发和死亡,建议定期进行MRI检查。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号