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将小儿小脑脑肿瘤幸存者的长期认知和运动缺陷映射到小脑白质图谱中。

Mapping of long-term cognitive and motor deficits in pediatric cerebellar brain tumor survivors into a cerebellar white matter atlas.

机构信息

Charité-Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Pediatric Oncology and Hematology, Berlin, Germany.

Department of Neurosurgery, Universitätsklinikum Würzburg, Würzburg, Germany.

出版信息

Childs Nerv Syst. 2021 Sep;37(9):2787-2797. doi: 10.1007/s00381-021-05244-2. Epub 2021 Aug 5.


DOI:10.1007/s00381-021-05244-2
PMID:34355257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8423645/
Abstract

PURPOSE: Diaschisis of cerebrocerebellar loops contributes to cognitive and motor deficits in pediatric cerebellar brain tumor survivors. We used a cerebellar white matter atlas and hypothesized that lesion symptom mapping may reveal the critical lesions of cerebellar tracts. METHODS: We examined 31 long-term survivors of pediatric posterior fossa tumors (13 pilocytic astrocytoma, 18 medulloblastoma). Patients underwent neuronal imaging, examination for ataxia, fine motor and cognitive function, planning abilities, and executive function. Individual consolidated cerebellar lesions were drawn manually onto patients' individual MRI and normalized into Montreal Neurologic Institute (MNI) space for further analysis with voxel-based lesion symptom mapping. RESULTS: Lesion symptom mapping linked deficits of motor function to the superior cerebellar peduncle (SCP), deep cerebellar nuclei (interposed nucleus (IN), fastigial nucleus (FN), ventromedial dentate nucleus (DN)), and inferior vermis (VIIIa, VIIIb, IX, X). Statistical maps of deficits of intelligence and executive function mapped with minor variations to the same cerebellar structures. CONCLUSION: We identified lesions to the SCP next to deep cerebellar nuclei as critical for limiting both motor and cognitive function in pediatric cerebellar tumor survivors. Future strategies safeguarding motor and cognitive function will have to identify patients preoperatively at risk for damage to these critical structures and adapt multimodal therapeutic options accordingly.

摘要

目的:大脑-小脑回路的去传入现象导致小儿小脑脑肿瘤幸存者认知和运动功能缺陷。我们使用小脑白质图谱,并假设病灶症状映射可能揭示小脑束的关键病灶。

方法:我们检查了 31 例儿童后颅窝肿瘤(13 例毛细胞星形细胞瘤,18 例髓母细胞瘤)的长期幸存者。患者接受了神经元成像、共济失调检查、精细运动和认知功能、计划能力和执行功能检查。将个体的巩固性小脑病灶手动绘制到患者的个体 MRI 上,并归一化为蒙特利尔神经学研究所(MNI)空间,以便进一步进行基于体素的病灶症状映射分析。

结果:病灶症状映射将运动功能缺陷与上小脑脚(SCP)、深部小脑核(间位核(IN)、顶核(FN)、腹内侧齿状核(DN))和下蚓部(VIIIa、VIIIb、IX、X)联系起来。智力和执行功能缺陷的统计图谱以较小的变化映射到相同的小脑结构。

结论:我们确定了 SCP 旁边的深部小脑核的病灶是限制小儿小脑肿瘤幸存者运动和认知功能的关键。未来保护运动和认知功能的策略将需要在术前识别出有这些关键结构损伤风险的患者,并相应地调整多模态治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec01/8423645/dbfbfe129b2d/381_2021_5244_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec01/8423645/8b62a03197e6/381_2021_5244_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec01/8423645/ef45f11930ba/381_2021_5244_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec01/8423645/dbfbfe129b2d/381_2021_5244_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec01/8423645/8b62a03197e6/381_2021_5244_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec01/8423645/ef45f11930ba/381_2021_5244_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec01/8423645/dbfbfe129b2d/381_2021_5244_Fig3_HTML.jpg

相似文献

[1]
Mapping of long-term cognitive and motor deficits in pediatric cerebellar brain tumor survivors into a cerebellar white matter atlas.

Childs Nerv Syst. 2021-9

[2]
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[3]
Cerebral white matter fractional anisotropy and tract volume as measured by MR imaging are associated with impaired cognitive and motor function in pediatric posterior fossa tumor survivors.

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[4]
Loss of fine motor function correlates with ataxia and decline of cognition in cerebellar tumor survivors.

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[5]
Morphological brain lesions of pediatric cerebellar tumor survivors correlate with inferior neurocognitive function but do not affect health-related quality of life.

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[6]
Resection of cerebellar tumours causes widespread and functionally relevant white matter impairments.

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[7]
Executive function deficits in pediatric cerebellar tumor survivors.

Eur J Paediatr Neurol. 2016-1

[8]
Neuroimaging of the component white matter connections and structures within the cerebellar-frontal pathway in posterior fossa tumor survivors.

Neuroimage Clin. 2019-6-10

[9]
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[10]
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引用本文的文献

[1]
Visual-Motor Functions and Associated Cognitive Outcomes in Pediatric Cancer Survivors.

Med Sci (Basel). 2025-4-5

[2]
Causally Mapping the Cerebellum in Children and Young Adults: from Motor to Cognition.

Cerebellum. 2025-1-16

[3]
Cognitive outcome and its neural correlates after cardiorespiratory arrest in childhood.

Dev Sci. 2024-7

[4]
Large-scale brain networks and intra-axial tumor surgery: a narrative review of functional mapping techniques, critical needs, and scientific opportunities.

Front Hum Neurosci. 2023-7-13

[5]
Automatic detection and segmentation of postoperative cerebellar damage based on normalization.

Neurooncol Adv. 2023-1-28

[6]
Networking of the Human Cerebellum: From Anatomo-Functional Development to Neurosurgical Implications.

Front Neurol. 2022-2-4

本文引用的文献

[1]
Resection of cerebellar tumours causes widespread and functionally relevant white matter impairments.

Hum Brain Mapp. 2021-4-15

[2]
Reliable tumor detection by whole-genome methylation sequencing of cell-free DNA in cerebrospinal fluid of pediatric medulloblastoma.

Sci Adv. 2020-10

[3]
Outcomes of BRAF V600E Pediatric Gliomas Treated With Targeted BRAF Inhibition.

JCO Precis Oncol. 2020-5-20

[4]
Living with the cerebellar mutism syndrome: long-term challenges of the diagnosis.

Acta Neurochir (Wien). 2021-5

[5]
Role of neoadjuvant chemotherapy in metastatic medulloblastoma: a comparative study in 92 children.

Neuro Oncol. 2020-11-26

[6]
Preoperative prediction of postoperative cerebellar mutism syndrome. Validation of existing MRI models and proposal of the new Rotterdam pCMS prediction model.

Childs Nerv Syst. 2020-7

[7]
Pediatric postoperative cerebellar cognitive affective syndrome follows outflow pathway lesions.

Neurology. 2019-9-16

[8]
Post-operative cerebellar mutism syndrome: rehabilitation issues.

Childs Nerv Syst. 2020-6

[9]
Medulloblastoma.

Nat Rev Dis Primers. 2019-2-14

[10]
PPAR and GST polymorphisms may predict changes in intellectual functioning in medulloblastoma survivors.

J Neurooncol. 2019-1-3

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