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儿童低级别星形细胞瘤治疗后的功能转归

Functional outcome after low-grade astrocytoma treatment in childhood.

作者信息

Aarsen Femke K, Paquier Philippe F, Reddingius Roel E, Streng Isabelle C, Arts Willem-Frans M, Evera-Preesman Marjon, Catsman-Berrevoets Coriene E

机构信息

Department of Pediatric Neurology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.

出版信息

Cancer. 2006 Jan 15;106(2):396-402. doi: 10.1002/cncr.21612.

Abstract

BACKGROUND

The relatively high survival rate of patients with low-grade astrocytoma necessitates increasing attention to physical and psychosocial outcomes. The objective of the current study was to investigate functional outcomes among children who were treated for low-grade or pilocytic astrocytoma in different areas of the brain.

METHODS

Functional outcomes were evaluated in the following domains: impairments, disabilities, handicaps, and quality of life (QOL). In a consecutive series, 38 children were included. Follow-up ranged from 3 years and 7 months to 11 years and 4 months after diagnosis.

RESULTS

Approximately 61% of children had impairments and 10% had a severe disability. Handicaps were found in the domains of relationships, school, and behavior. Children who were treated for supratentorial tumors required significantly more special education, and children who were treated for infratentorial tumors had significantly more behavioral and social problems. QOL was decreased significantly in all domains except emotions. Children who had a diagnosis in adolescence reported a lower QOL in social functioning compared with younger children. Data analysis revealed that some deficits suddenly became apparent years after diagnosis.

CONCLUSIONS

At long-term follow-up, children who had low-grade or pilocytic astrocytomas were found to have poor functional outcomes, depending on tumor site, age, and recurrence. Children without deficits may develop severe cognitive, social, and behavioral deficits years after diagnosis, because of the phenomenon of "growing into deficit." Therefore, the authors suggest a long-term follow-up of children who are treated for low-grade or pilocytic astrocytomas at a young age to detect and subsequently offer support focused on the medical and cognitive impairments as well as on the behavioral and social consequences of their disease.

摘要

背景

低级别星形细胞瘤患者相对较高的生存率使得对其身体和心理社会结局的关注日益增加。本研究的目的是调查在大脑不同区域接受低级别或毛细胞型星形细胞瘤治疗的儿童的功能结局。

方法

在以下领域评估功能结局:损伤、残疾、障碍和生活质量(QOL)。纳入了连续系列的38名儿童。随访时间为诊断后3年7个月至11年4个月。

结果

约61%的儿童有损伤,10%有严重残疾。在人际关系、学校和行为领域发现了障碍。幕上肿瘤接受治疗的儿童需要显著更多的特殊教育,幕下肿瘤接受治疗的儿童有显著更多的行为和社会问题。除情感领域外,所有领域的生活质量均显著下降。与年幼儿童相比,青春期确诊的儿童在社会功能方面的生活质量较低。数据分析显示,一些缺陷在诊断后数年突然变得明显。

结论

在长期随访中,发现低级别或毛细胞型星形细胞瘤患儿的功能结局较差,这取决于肿瘤部位、年龄和复发情况。由于“发展为缺陷”现象,无缺陷的儿童在诊断后数年可能会出现严重的认知、社会和行为缺陷。因此,作者建议对幼年时接受低级别或毛细胞型星形细胞瘤治疗的儿童进行长期随访,以检测并随后提供针对医疗和认知损伤以及其疾病的行为和社会后果的支持。

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