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Quantitative MRI in post-operative paediatric cerebellar mutism syndrome.
Toescu, Sebastian M; Hales, Patrick W; Aquilina, Kristian; Clark, Chris A.
Afiliación
  • Toescu SM; Developmental Imaging and Biophysics Section, UCL GOS Institute of Child Health, 30 Guilford Street, London WC1N 1EH, United Kingdom; Department of Neurosurgery, Great Ormond Street Hospital for Children, Great Ormond Street, London WC1N 3JH, United Kingdom. Electronic address: sebastian.toescu@ucl.
  • Hales PW; Developmental Imaging and Biophysics Section, UCL GOS Institute of Child Health, 30 Guilford Street, London WC1N 1EH, United Kingdom. Electronic address: p.hales@ucl.ac.uk.
  • Aquilina K; Department of Neurosurgery, Great Ormond Street Hospital for Children, Great Ormond Street, London WC1N 3JH, United Kingdom. Electronic address: kristian.aquilina@gosh.nhs.uk.
  • Clark CA; Developmental Imaging and Biophysics Section, UCL GOS Institute of Child Health, 30 Guilford Street, London WC1N 1EH, United Kingdom. Electronic address: christopher.clark@ucl.ac.uk.
Eur J Radiol ; 108: 43-51, 2018 Nov.
Article en En | MEDLINE | ID: mdl-30396670
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cerebelosas / Mutismo Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Eur J Radiol Año: 2018 Tipo del documento: Article Pais de publicación: Irlanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cerebelosas / Mutismo Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Eur J Radiol Año: 2018 Tipo del documento: Article Pais de publicación: Irlanda