Quantitative MRI in post-operative paediatric cerebellar mutism syndrome

被引:16
|
作者
Toescu, Sebastian M. [1 ,2 ]
Hales, Patrick W. [1 ]
Aquilina, Kristian [2 ]
Clark, Chris A. [1 ]
机构
[1] UCL GOS Inst Child Hlth, Dev Imaging & Biophys Sect, 30 Guilford St, London WC1N 1EH, England
[2] Great Ormond St Hosp Sick Children, Dept Neurosurg, Great Ormond St, London WC1N 3JH, England
关键词
Cerebellar mutism; Posterior fossa syndrome; Medulloblastoma; Tractography; Arterial spin labelling; POSTERIOR-FOSSA SYNDROME; MATTER FIBER TRACTOGRAPHY; TUMOR RESECTION; RISK-FACTORS; CHILDREN; SURGERY; TRACT; MEDULLOBLASTOMA; PREDICTOR; PATHOPHYSIOLOGY;
D O I
10.1016/j.ejrad.2018.09.007
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Post-operative paediatric cerebellar mutism syndrome (pCMS) occurs in around 25% of children undergoing surgery for cerebellar and fourth ventricular tumours. Reversible mutism is the hallmark of a syndrome which comprises severe motor, cognitive and linguistic deficits. Recent evidence from advanced neuroimaging studies has led to the current theoretical understanding of the condition as a form of diaschisis contingent on damage to efferent cerebellar circuitry. Tractography data derived from diffusion MRI studies have shown disruption of the dentato-rubro-thalamo-cortical tract in patients with pCMS, and perfusion studies have indicated widespread supratentorial regions which may give rise to the florid signs and symptoms of pCMS. Given the difficulties in predicting pCMS from standard structural MRI, this review discusses findings from quantitative MRI modalities which have contributed to our understanding of this debilitating syndrome, and considers the goals and challenges which lie ahead in the field.
引用
收藏
页码:43 / 51
页数:9
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