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与小脑缄默症相关的手术及磁共振成像因素分析

Analysis of surgical and MRI factors associated with cerebellar mutism.

作者信息

Sergeant Anjali, Kameda-Smith Michelle Masayo, Manoranjan Branavan, Karmur Brij, Duckworth JoAnn, Petrelli Tina, Savage Katey, Ajani Olufemi, Yarascavitch Blake, Samaan M Constantine, Scheinemann Katrin, Alyman Cheryl, Almenawer Saleh, Farrokhyar Forough, Fleming Adam J, Singh Sheila Kumari, Stein Nina

机构信息

McMaster Pediatric Brain Tumor Study Group, McMaster University, Hamilton, Canada.

Department of Surgery, Division of Neurosurgery, McMaster University, Hamilton, Canada.

出版信息

J Neurooncol. 2017 Jul;133(3):539-552. doi: 10.1007/s11060-017-2462-4. Epub 2017 May 19.

DOI:10.1007/s11060-017-2462-4
PMID:28527006
Abstract

The surgical risk factors and neuro-imaging characteristics associated with cerebellar mutism (CM) remain unclear and require further investigation. Therefore, we aimed to examine surgical and MRI findings associated with CM in children following posterior fossa tumor resection. Using our data registry, we retrospectively collected data from pediatric patients who acquired CM and were matched based on age and pathology type with individuals who did not acquire CM after posterior fossa surgery. The strength of association between surgical and MRI variables and CM were examined using odds ratios (ORs) and corresponding 95% confidence intervals (CIs). A total of 22 patients (11 with and 11 without CM) were included. Medulloblastoma was the most common pathology among CM patients (91%); the remaining 9% were diagnosed with a pilocytic astrocytoma. Tumor attachment to the floor of the fourth ventricle (OR 6; 95% CI 0.7-276), calcification/hemosiderin deposition (OR 7; 95% CI 0.9-315.5), and post-operative peri-ventricular ischemia on MRI (OR 5; 95% CI 0.5-236.5) were found to have the highest measures of association with CM. Our results may suggest that tumor attachment to the floor of the fourth ventricle, pathological calcification, and post-operative ischemia have a relatively higher prevalence in patients with CM. Collectively, our work calls for a larger multi-institutional cohort study of CM patients to encourage further investigation of the determinants and management of CM in order to potentially minimize its development and predict onset.

摘要

与小脑缄默症(CM)相关的手术风险因素和神经影像学特征仍不明确,需要进一步研究。因此,我们旨在研究后颅窝肿瘤切除术后儿童中与CM相关的手术和MRI表现。利用我们的数据登记系统,我们回顾性收集了发生CM的儿科患者的数据,并根据年龄和病理类型与后颅窝手术后未发生CM的个体进行匹配。使用优势比(OR)和相应的95%置信区间(CI)来检验手术和MRI变量与CM之间的关联强度。共纳入22例患者(11例发生CM,11例未发生CM)。髓母细胞瘤是CM患者中最常见的病理类型(91%);其余9%被诊断为毛细胞型星形细胞瘤。发现肿瘤附着于第四脑室底部(OR 6;95% CI 0.7 - 276)、钙化/含铁血黄素沉积(OR 7;95% CI 0.9 - 315.5)以及MRI上术后脑室周围缺血(OR 5;95% CI 0.5 - 236.5)与CM的关联度最高。我们的结果可能表明,肿瘤附着于第四脑室底部、病理性钙化和术后缺血在CM患者中相对更为常见。总体而言,我们的工作呼吁对CM患者进行更大规模的多机构队列研究,以鼓励进一步研究CM的决定因素和管理方法,从而有可能尽量减少其发生并预测其发作。

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Asian J Neurosurg. 2025 Jan 13;20(2):260-268. doi: 10.1055/s-0044-1801404. eCollection 2025 Jun.
2
Neuroimaging of postoperative pediatric cerebellar mutism syndrome: a systematic review.小儿术后小脑缄默综合征的神经影像学:一项系统评价
Neurooncol Adv. 2024 Dec 14;7(1):vdae212. doi: 10.1093/noajnl/vdae212. eCollection 2025 Jan-Dec.
3
National multicentered retrospective review of clinical and intraoperative factors associated with the development of cerebellar mutism after pediatric posterior fossa tumor resection.

本文引用的文献

1
Longitudinal cerebellar diffusion tensor imaging changes in posterior fossa syndrome.后颅窝综合征中小脑的纵向扩散张量成像变化
Neuroimage Clin. 2016 Sep 9;12:582-590. doi: 10.1016/j.nicl.2016.09.007. eCollection 2016.
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Intellectual Outcome in Molecular Subgroups of Medulloblastoma.脑胶质瘤分子亚群的智力预后。
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Prognostic value of medulloblastoma extent of resection after accounting for molecular subgroup: a retrospective integrated clinical and molecular analysis.
全国多中心回顾性研究分析了与儿童后颅窝肿瘤切除术后小脑缄默症发展相关的临床和术中因素。
Childs Nerv Syst. 2024 May;40(5):1339-1347. doi: 10.1007/s00381-024-06292-0. Epub 2024 Jan 27.
4
Posterior fossa syndrome in a population of children and young adults with medulloblastoma: a retrospective, multicenter Italian study on incidence and pathophysiology in a histologically homogeneous and consecutive series of 136 patients.小脑髓母细胞瘤患儿和青年患者的后颅窝综合征:一项回顾性、多中心意大利研究,分析 136 例组织学上同质且连续的患者中的发生率和病理生理学
J Neurooncol. 2022 Sep;159(2):377-387. doi: 10.1007/s11060-022-04072-x. Epub 2022 Jun 29.
5
The Role of a Longitudinal, Multidisciplinary Clinic in Building a Unique Research Collaborative.纵向多学科诊所 在建立独特研究合作中的作用
Front Oncol. 2022 Apr 8;12:857699. doi: 10.3389/fonc.2022.857699. eCollection 2022.
6
Individual cerebrocerebellar functional network analysis decoding symptomatologic dynamics of postoperative cerebellar mutism syndrome.个体脑桥小脑功能网络分析解码术后小脑缄默综合征的症状学动态变化。
Cereb Cortex Commun. 2022 Feb 11;3(1):tgac008. doi: 10.1093/texcom/tgac008. eCollection 2022.
7
Association between cerebral perfusion and paediatric postoperative cerebellar mutism syndrome after posterior fossa surgery-a systematic review.脑血流与后颅窝手术后小儿术后小脑缄默综合征的关系:系统评价。
Childs Nerv Syst. 2021 Sep;37(9):2743-2751. doi: 10.1007/s00381-021-05225-5. Epub 2021 Jun 21.
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Establishing reproducible predictors of cerebellar mutism syndrome based on pre-operative imaging.基于术前影像学建立小脑缄默综合征的可重复性预测指标。
Childs Nerv Syst. 2019 May;35(5):795-800. doi: 10.1007/s00381-019-04075-6. Epub 2019 Feb 6.
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Hypertrophic olivary degeneration in children after posterior fossa surgery. An underdiagnosed condition.儿童后颅窝手术后的肥大性橄榄核变性。一种诊断不足的病症。
Childs Nerv Syst. 2018 Mar;34(3):409-415. doi: 10.1007/s00381-017-3705-6. Epub 2017 Dec 26.
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Childs Nerv Syst. 2015 Oct;31(10):1853-8. doi: 10.1007/s00381-015-2796-1. Epub 2015 Jul 5.
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Diffusion abnormalities on intraoperative magnetic resonance imaging as an early predictor for the risk of posterior fossa syndrome.术中磁共振成像上的扩散异常作为后颅窝综合征风险的早期预测指标。
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J Neurosurg Pediatr. 2013 Dec;12(6):604-14. doi: 10.3171/2013.8.PEDS13168. Epub 2013 Sep 27.
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Time-dependent structural changes of the dentatothalamic pathway in children treated for posterior fossa tumor.儿童后颅窝肿瘤治疗后齿状核-丘脑束的时间依赖性结构变化。
AJNR Am J Neuroradiol. 2014 Apr;35(4):803-7. doi: 10.3174/ajnr.A3735. Epub 2013 Sep 19.