Your browser doesn't support javascript.
loading
Secondary cerebro-cerebellar and intracerebellar dysfunction in cerebellar mutism syndrome.
McAfee, Samuel S; Robinson, Giles; Gajjar, Amar; Phillips, Nicholas S; Zhang, Silu; Zou Stinnett, Ping; Sitaram, Ranganatha; Raches, Darcy; Conklin, Heather M; Khan, Raja B; Scoggins, Matthew A.
Affiliation
  • McAfee SS; Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Robinson G; Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Gajjar A; Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Phillips NS; Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Zhang S; Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Zou Stinnett P; Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Sitaram R; Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Raches D; Department of Psychology and Biobehavioral Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Conklin HM; Department of Psychology and Biobehavioral Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Khan RB; Division of Neurology, Department of Pediatrics, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
  • Scoggins MA; Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Neuro Oncol ; 2024 Apr 06.
Article in En | MEDLINE | ID: mdl-38581226
ABSTRACT

BACKGROUND:

Cerebellar mutism syndrome (CMS) is characterized by deficits of speech, movement, and affect that can occur following tumor removal from the posterior fossa. The role of cerebrocerebellar tract injuries in the etiology of CMS remains unclear, with recent studies suggesting that cerebrocerebellar dysfunction may be related to chronic, rather than transient, symptomatology.

METHODS:

We measured functional connectivity between the cerebellar cortex and functional nodes throughout the brain using fMRI acquired after tumor removal but prior to adjuvant therapy in a cohort of 70 patients diagnosed with medulloblastoma. Surgical lesions were mapped to the infratentorial anatomy, and connectivity with cerebral cortex was tested for statistical dependence on extent of cerebellar outflow pathway injury.

RESULTS:

CMS diagnosis was associated with an increase in connectivity between the right cerebellar and left cerebral hemisphere, maximally between cerebellum and ventromedial prefrontal cortex (VM-PFC). Connectivity dependence on cerebellar outflow was significant for some speech nodes but not for VM-PFC, suggesting altered input to the cerebellum. Connectivity between posterior regions of cerebellar cortex and ipsilateral dentate nuclei was abnormal in CMS participants, maximally within the right cerebellar hemisphere.

CONCLUSIONS:

The functional abnormalities we identified are notably upstream of where causal surgical injury is thought to occur, indicating a secondary phenomenon. The VM-PFC is involved in several functions that may be relevant to the symptomatology of CMS, including emotional control and motor learning. We hypothesize that these abnormalities may reflect maladaptive learning within the cerebellum consequent to disordered motor and limbic function by the periaqueductal grey and other critical midbrain targets.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Neuro Oncol Journal subject: NEOPLASIAS / NEUROLOGIA Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Neuro Oncol Journal subject: NEOPLASIAS / NEUROLOGIA Year: 2024 Document type: Article Affiliation country:
...