Structural damage burden and hypertrophic olivary degeneration in pediatric postoperative cerebellar mutism syndrome

被引:0
作者
Thomas Beez
Christopher Munoz-Bendix
Hendrik-Jan Mijderwijk
Marc Remke
Daniel Hänggi
机构
[1] Heinrich-Heine-University,Department of Neurosurgery, Medical Faculty
[2] Heinrich-Heine-University,Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty
来源
Neurosurgical Review | 2022年 / 45卷
关键词
Cerebellar mutism syndrome; Posterior fossa tumor; Children; Hypertrophic olivary degeneration; Dentate nucleus; Superior cerebellar peduncle; Personalized medicine;
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学科分类号
摘要
Cerebellar mutism syndrome (CMS) occurs in one out of four children after posterior fossa tumor surgery, with open questions regarding risk factors, pathophysiology, and prevention strategies. Because of similarities between several cerebellar syndromes, a common pathophysiology with damage to the dentato-thalamo-cortical and dentato-rubro-olivary pathways has been proposed. Hypertrophic olivary degeneration (HOD) is an imaging correlate of cerebellar injury observed for instance in stroke patients. Aim of this study was to investigate whether the occurrence and severity of CMS correlates with the extent of damage to the relevant anatomical structures and whether HOD is a time-dependent postoperative neuroimaging correlate of CMS. We performed a retrospective single center study of CMS patients compared with matched non-CMS controls. CMS occurred in 10 children (13% of the overall cohort) with a median age of 8 years. Dentate nucleus (DN) injury significantly correlated with CMS, and superior cerebellar peduncle (SCP) injury was associated by tendency. HOD was observed as a dynamic neuroimaging phenomenon in the postoperative course and its presence significantly correlated with CMS and DN injury. Children who later developed HOD had an earlier onset and tended to have longer persistence of CMS. These findings can guide surgical measures to protect the DN and SCP during posterior fossa tumor resections and to avoid a high damage burden (i.e., bilateral damage). Development of intraoperative neuromonitoring of the cerebellar efferent pathways as well as improved preoperative risk stratification could help to establish a patient-specific strategy with optimal balance between degree of resection and functional integrity.
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页码:2757 / 2765
页数:8
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共 217 条
[1]  
Ahmadian N(2021)Association between cerebral perfusion and paediatric postoperative cerebellar mutism syndrome after posterior fossa surgery—a systematic review Child’s Nerv Syst 37 2743-2751
[2]  
van Baarsen KM(2019)Intraoperative assessment of isocitrate dehydrogenase mutation status in human gliomas using desorption electrospray ionization-mass spectrometry J Neurosurg 132 180-187
[3]  
Robe PAJT(2016)Post-operative pediatric cerebellar mutism syndrome and its association with hypertrophic olivary degeneration Quant Imaging Med Surg 6 535-544
[4]  
Hoving EW(2021)Functional tracts of the cerebellum-essentials for the neurosurgeon Neurosurg Rev 44 273-278
[5]  
Alfaro CM(2017)Cerebellar mutism syndrome: cause and rehabilitation Curr Opin Neurol 30 133-139
[6]  
Pirro V(1995)The pathophysiology of oral pharyngeal apraxia and mutism following posterior fossa tumor resection in children J Neurosurg 83 467-475
[7]  
Keating MF(2021)Feasibility of cerebello-cortical stimulation for intraoperative neurophysiological monitoring of cerebellar mutism Childs Nerv Syst 37 1505-1514
[8]  
Hattab EM(2000)Hypertrophic olivary degeneration: metaanalysis of the temporal evolution of MR findings Am J Neuroradiol 21 1073-1077
[9]  
Cooks RG(2000)Hypertrophic olivary degeneration: metaanalysis of the temporal evolution of MR findings AJNR Am J Neuroradiol 21 1073-1077
[10]  
Cohen-Gadol AA(2011)Cerebellar mutism: definitions, classification and grading of symptoms Child’s Nerv Syst 27 1361-1363