Meeting Banner
Abstract #4198

Evaluation of Cerebrocerebellar Pathway Integrity in Pediatric Posterior Fossa Tumor Patients with Cerebellar Mutism Syndrome

Nicole Law1,2, Eric Bouffet3, Douglas Strother4, Suzanne Laughlin5, Normand Laperriere6, Marie-Eve Briere4, Dina McConnell7, Juliette Hukin8, Christopher Fryer8, Conrad Rockel1, Fang Liu1, Donald Mabbott1,9

1Department of Psychology, Program in Neuroscience & Mental Health, the Hospital for Sick Children, Toronto, Ontario, Canada; 2Department of Psychology, Collaborative Program in Neuroscience, University of Toronto, Toronto, Ontario, Canada; 3Department of Haematology/Oncology, the Hospital for Sick Children, Toronto, Ontario, Canada; 4Southern Alberta Cancer Program, Alberta Children's Hospital, Calgary, Alberta, Canada; 5Diagnostic Imaging, the Hospital for Sick Children, Toronto, Ontario, Canada; 6Radiation Oncology, Princess Margaret Hospital, Toronto, Ontario, Canada; 7Department of Psychology, British Columbia Children's Hospital, Vancouver, British Columbia, Canada; 8Department of Oncology, British Columbia Children's Hospital, Vancouver, British Columbia, Canada; 9Department of Psychology, University of Toronto, Toronto, Ontario, Canada


Cerebellar Mutism Syndrome (CMS) can be observed following resection of posterior fossa (PF) tumors and presents with abnormalities in speech/language production, cognition, and emotion. We examined differences in the integrity of input/output pathways connecting the cerebellum with cerebral regions in patients with CMS relative to patients without CMS and healthy controls using diffusion tensor imaging tractography. The cerebrocerebellar pathway connecting the right cerebellar hemisphere with left frontal regions showed greater damage in patients with CMS versus the other groups. Our findings suggest that the pathway connecting the cerebellum with areas of the brain important for language is disrupted in CMS.