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Objective: A single-institution cohort of 92 consecutive pediatric patients harboring tumors involving the fourth ventricle, surgically treated the telovelar or transvermian approach, was retrospectively reviewed in order to analyze the impact of surgical route on surgery-related outcomes and cumulative survival.
Methods: Clinical, radiological, surgical, and pathology details were retrospectively analyzed. We selected n = 6 surgery-related clinical and radiological outcomes: transient and permanent neurological deficits, duration of assisted ventilation, postoperative new onset medical events, postoperative cerebellar mutism, and extent of resection. We built univariate and multivariate logistic models to analyze the significance of relationships between the surgical routes and the outcomes. Cumulative survival (CS) was estimated by the cohort approach.
Results: There were 53 girls and 39 boys (mean age, 83 months). Telovelar approach was performed in 51 cases and transvermian approach in 41 cases. Early postoperative MRI studies showed complete removal in 57 cases (62%) and measurable residual tumor in 35 cases (38%). The average tumor residual volume was 1,316 cm (range, 0.016-4.231 cm; median value, 0.9875 cm). Residual disease was more often detected on immediate postop MRI after telovelar approach, but the difference was not significant. Cerebellar mutism was observed in 10 cases (11%). No significant difference in the onset of cerebellar mutism was detected between telovelar and transvermian approach. The choice of surgical approach did not significantly modify any other postoperative outcome and 1-/3-year CS of high-grade surgically treated tumors.
Conclusions: With the limitation of a single-center, single-surgeon retrospective series, our findings offer significant data to reconsider the real impact of the choice of the surgical route to the fourth ventricle on the incidence of cerebellar mutism and surgery-related morbidity. This seems to be in line with some recent reports in the literature. Surgical approach to the fourth ventricle should be individualized according to the location of the tumor, degree of vermian infiltration, and lateral and upward extension. Telovelar and transvermian approaches should not be considered alternative but complementary. Pediatric neurosurgeons should fully master both approaches and choose the one that they consider the best for the patient based on a thorough and careful evaluation of pre-operative imaging.
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http://dx.doi.org/10.3389/fonc.2022.821738 | DOI Listing |
Dev Med Child Neurol
September 2025
Neuropsychology Service, Psychological and Mental Health Services, Great Ormond Street Hospital, London, UK.
Aim: To systematically review neurocognitive outcomes associated with postoperative paediatric cerebellar mutism syndrome (pCMS), comparing children with and without pCMS after posterior fossa tumour surgery, and in relation to moderating demographic and clinical risk factors.
Method: PsycInfo, Medline, and Embase databases were systematically searched up to December 2024. Studies of children aged 2 to 18 years with pCMS who had undergone standardized neurocognitive assessment were included.
BMC Psychiatry
July 2025
Department of Neurology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8677, Japan.
Background: Catatonia is a psychomotor disorder characterized by diverse clinical features, including mutism, stereotypy, posturing, waxy flexibility, and echophenomena. This condition is often observed in patients with anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis, in which impaired glutamatergic transmission through antibody-mediated NMDAR internalization is demonstrated. However, cases of anti-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) encephalitis presenting as catatonia have rarely been reported, and the mechanisms underlying such presentation remain unclear.
View Article and Find Full Text PDFPediatr Radiol
August 2025
Department of Radiology, Alder Hey Children's NHS Foundation Trust, Liverpool, United Kingdom.
Background: Cerebellar mutism syndrome is a well-known complication of paediatric posterior fossa tumour surgery. In recent years, several imaging biomarkers have been suggested to predict cerebellar mutism syndrome based on its probable pathoanatomical causes.
Objective: This study investigates the reliability of preoperative imaging biomarkers for cerebellar mutism syndrome in paediatric posterior fossa tumours.
Childs Nerv Syst
July 2025
Department of Paediatrics and Adolescent Medicine, The University Hospital Rigshospitalet, Blegdamsvej 9, DK-2100, Copenhagen E, Denmark.
Purpose: Postoperative speech impairment (POSI) is a core symptom of cerebellar mutism syndrome (CMS) and is a common complication after the resection of paediatric posterior fossa (PF) tumours. Preoperative glucocorticoids (pGC) are considered standard treatment to reduce tumour oedema; in addition, glucocorticoids are often administered intraoperatively (iGC) to reduce both postoperative nausea and vomiting. The study aims to investigate whether the occurrence of POSI may be associated with pGC and iGC.
View Article and Find Full Text PDFChildren (Basel)
May 2025
Department of Neurosurgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
To develop and validate a composite model that combines lesion-symptom mapping (LSM), radiomic information, and clinical factors for predicting cerebellar mutism syndrome in pediatric patients suffering from posterior fossa tumors. A retrospective analysis was conducted on a cohort of 247 (training set, = 174; validation set, = 73) pediatric patients diagnosed with posterior fossa tumors who underwent surgery at Beijing Children's Hospital. Presurgical MRIs were used to extract the radiomics features and voxel distribution features.
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