Suppr超能文献

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。

Diffusion abnormalities on intraoperative magnetic resonance imaging as an early predictor for the risk of posterior fossa syndrome.

作者信息

Avula Shivaram, Kumar Ram, Pizer Barry, Pettorini Benedetta, Abernethy Laurence, Garlick Deborah, Mallucci Conor

机构信息

Department of Radiology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK (S.A., L.A., D.G.); Department of Neurology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK (R.K.); Department of Oncology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK (Barry Pizer); Department of Neurosurgery, Alder Hey Children's N.H.S Foundation Trust, Liverpool, UK (Benedetta Pettorini, C.M.).

出版信息

Neuro Oncol. 2015 Apr;17(4):614-22. doi: 10.1093/neuonc/nou299. Epub 2014 Oct 15.

Abstract

BACKGROUND

Posterior fossa syndrome (PFS) is an important complication of posterior fossa surgery in children. The pathophysiology of this condition remains unclear, but there is evidence implicating surgical injury of the proximal efferent cerebellar pathway (pECP) and the cerebellar vermis to PFS. We aimed to evaluate if diffusion abnormalities involving these structures on the final intraoperative MRI can predict the development of PFS.

METHODS

Diffusion-weighted imaging from 31 posterior fossa resections were anonymized and evaluated for abnormalities involving the dentate nucleus, superior cerebellar peduncle, and the mesencephalic tegmentum forming the pECP, vermis, and middle cerebellar peduncle. The case notes were independently evaluated for evidence of PFS.

RESULTS

The diffusion imaging in 28 cases was of optimal quality for evaluation. Diffusion abnormalities were identified in 10 cases, 7 of which involved the pECP. Retrospective evaluation revealed evidence of PFS in 6 cases. There was a significant association between abnormalities involving pECP structures (P = .001) and development of PFS. Bilateral involvement of pECP (P = .006) was a highly specific risk factor for predicting the development of PFS. Diffusion abnormality of the inferior vermis was significantly associated with PFS (P = .001) but may not represent a risk factor in isolation.

CONCLUSION

This study demonstrates the feasibility of identifying children at risk for developing PFS at the earliest stage post tumor resection and thus adds to the growing evidence base on its pathophysiology.

摘要

背景

后颅窝综合征(PFS)是儿童后颅窝手术的一种重要并发症。这种病症的病理生理学仍不清楚,但有证据表明,小脑传出近端通路(pECP)和小脑蚓部的手术损伤与PFS有关。我们旨在评估术中最后阶段的磁共振成像(MRI)上涉及这些结构的扩散异常是否能预测PFS的发生。

方法

对31例后颅窝切除术的扩散加权成像进行匿名处理,并评估是否存在涉及齿状核、小脑上脚以及构成pECP、蚓部和小脑中脚的中脑被盖的异常情况。对病例记录进行独立评估,以寻找PFS的证据。

结果

28例病例的扩散成像质量达到最佳评估标准。10例发现有扩散异常,其中7例涉及pECP。回顾性评估发现6例有PFS的证据。涉及pECP结构的异常与PFS的发生之间存在显著关联(P = 0.001)。pECP的双侧受累(P = 0.006)是预测PFS发生的一个高度特异性危险因素。小脑下蚓部的扩散异常与PFS显著相关(P = 0.001),但单独来看可能并不代表危险因素。

结论

本研究证明了在肿瘤切除后的最早阶段识别有发生PFS风险儿童的可行性,从而为其病理生理学的证据基础增添了内容。

相似文献

2
Diffusion tensor imaging of the superior cerebellar peduncle identifies patients with posterior fossa syndrome.
Childs Nerv Syst. 2013 Nov;29(11):2071-7. doi: 10.1007/s00381-013-2205-6. Epub 2013 Jul 2.
3
Posterior fossa syndrome with delayed MR evidence of unilateral superior cerebellar peduncle (SCP) damage.
Childs Nerv Syst. 2017 Mar;33(3):503-507. doi: 10.1007/s00381-016-3287-8. Epub 2016 Nov 9.
4
Postoperative posterior fossa syndrome: unraveling the etiology and underlying pathophysiology by using magnetic resonance imaging.
Childs Nerv Syst. 2015 Oct;31(10):1853-8. doi: 10.1007/s00381-015-2796-1. Epub 2015 Jul 5.
5
Post-operative diffusion weighted imaging as a predictor of posterior fossa syndrome permanence in paediatric medulloblastoma.
Childs Nerv Syst. 2017 Mar;33(3):457-465. doi: 10.1007/s00381-017-3356-7. Epub 2017 Feb 11.
6
Posterior fossa syndrome following brain tumour resection: review of pathophysiology and a new hypothesis on its pathogenesis.
Childs Nerv Syst. 2015 Oct;31(10):1859-67. doi: 10.1007/s00381-015-2797-0. Epub 2015 Sep 9.
9
Proximal dentatothalamocortical tract involvement in posterior fossa syndrome.
Brain. 2009 Nov;132(Pt 11):3087-95. doi: 10.1093/brain/awp241. Epub 2009 Oct 5.
10
Postoperative speech impairment and surgical approach to posterior fossa tumours in children: a prospective European multicentre cohort study.
Lancet Child Adolesc Health. 2021 Nov;5(11):814-824. doi: 10.1016/S2352-4642(21)00274-1. Epub 2021 Oct 6.

引用本文的文献

1
Neuroimaging of postoperative pediatric cerebellar mutism syndrome: a systematic review.
Neurooncol Adv. 2024 Dec 14;7(1):vdae212. doi: 10.1093/noajnl/vdae212. eCollection 2025 Jan-Dec.
2
Comparison of Echo Planar and Turbo Spin Echo Diffusion-Weighted Imaging in Intraoperative MRI.
J Magn Reson Imaging. 2025 Apr;61(4):1847-1857. doi: 10.1002/jmri.29614. Epub 2024 Oct 10.
3
Survival implications of postoperative restricted diffusion in high-grade glioma and limitations of intraoperative MRI detection.
J Neurooncol. 2024 Nov;170(2):419-428. doi: 10.1007/s11060-024-04767-3. Epub 2024 Sep 24.
4
Neuroanatomy of cerebellar mutism syndrome: the role of lesion location.
Brain Commun. 2024 Jun 5;6(4):fcae197. doi: 10.1093/braincomms/fcae197. eCollection 2024.
6
Medulloblastomas, CNS embryonal tumors, and cerebellar mutism syndrome: advances in care and future directions.
Childs Nerv Syst. 2023 Oct;39(10):2633-2647. doi: 10.1007/s00381-023-06112-x. Epub 2023 Aug 26.
7
The Cerebellar Mutism Syndrome: Risk Assessment, Prevention and Treatment.
Adv Tech Stand Neurosurg. 2023;46:65-94. doi: 10.1007/978-3-031-28202-7_4.
8
Advanced intraoperative MRI in pediatric brain tumor surgery.
Front Physiol. 2023 Apr 13;14:1098959. doi: 10.3389/fphys.2023.1098959. eCollection 2023.
10
Prevalence of dysphagia following posterior fossa tumour resection in children: the Alder Hey experience.
Childs Nerv Syst. 2023 Mar;39(3):609-616. doi: 10.1007/s00381-022-05774-3. Epub 2022 Dec 13.

本文引用的文献

1
MR imaging evaluation of inferior olivary nuclei: comparison of postoperative subjects with and without posterior fossa syndrome.
AJNR Am J Neuroradiol. 2014 Apr;35(4):797-802. doi: 10.3174/ajnr.A3762. Epub 2013 Nov 1.
2
Diffusion tensor imaging of the superior cerebellar peduncle identifies patients with posterior fossa syndrome.
Childs Nerv Syst. 2013 Nov;29(11):2071-7. doi: 10.1007/s00381-013-2205-6. Epub 2013 Jul 2.
3
Clinical and neuroanatomical predictors of cerebellar mutism syndrome.
Neuro Oncol. 2012 Oct;14(10):1294-303. doi: 10.1093/neuonc/nos160. Epub 2012 Sep 5.
4
Importance of intraoperative magnetic resonance imaging for pediatric brain tumor surgery.
Surg Neurol Int. 2012;3(Suppl 2):S65-72. doi: 10.4103/2152-7806.95417. Epub 2012 Apr 26.
5
Intraoperative 3-Tesla MRI in the management of paediatric cranial tumours--initial experience.
Pediatr Radiol. 2012 Feb;42(2):158-67. doi: 10.1007/s00247-011-2261-6. Epub 2011 Oct 16.
6
Cerebellar mutism: review of the literature.
Childs Nerv Syst. 2011 Mar;27(3):355-63. doi: 10.1007/s00381-010-1328-2.
8
Proximal dentatothalamocortical tract involvement in posterior fossa syndrome.
Brain. 2009 Nov;132(Pt 11):3087-95. doi: 10.1093/brain/awp241. Epub 2009 Oct 5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验