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Postoperative MRI features of cerebellar mutism syndrome: a retrospective cohort study.
Yang, Wei; Zhang, Hong; Cai, Yingjie; Peng, Xiaojiao; Sun, Hailang; Chen, Jiashu; Ying, Zesheng; Zhu, Kaiyi; Peng, Yun; Ge, Ming.
Afiliación
  • Yang W; 1Departments of Neurosurgery and.
  • Zhang H; 2Radiology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing.
  • Cai Y; 1Departments of Neurosurgery and.
  • Peng X; 1Departments of Neurosurgery and.
  • Sun H; 1Departments of Neurosurgery and.
  • Chen J; 1Departments of Neurosurgery and.
  • Ying Z; 1Departments of Neurosurgery and.
  • Zhu K; 3Department of Cardiology, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan; and.
  • Peng Y; 4Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
  • Ge M; 2Radiology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing.
J Neurosurg Pediatr ; 30(6): 567-577, 2022 12 01.
Article en En | MEDLINE | ID: mdl-36208442
ABSTRACT

OBJECTIVE:

In this study, the authors aimed to investigate the relationship between postoperative MRI features and cerebellar mutism syndrome.

METHODS:

A retrospective cohort of patients who underwent tumor resection from July 2013 to March 2021 for midline posterior fossa tumors was investigated. All patients were followed up at least once. Clinical data were extracted from medical records and follow-up databases. Two neuroradiologists independently reviewed preoperative and postoperative MRI. Univariable and multivariable analyses were performed to compare the postoperative cerebellar mutism syndrome (pCMS) and non-pCMS groups. Correlation analysis was performed using the Spearman correlation coefficient analysis.

RESULTS:

Of 124 patients, 47 (37.9%) developed pCMS. The median follow-up duration was 45.73 (Q1 33.4, Q3 64.0) months. The median duration of mutism was 45 days. The median tumor size was 48.8 (Q1 42.1, Q3 56.8) mm. In the univariable analysis, abnormal T2-weighted signal of the left dentate nucleus (DN) (74.5% in the pCMS group vs 36.4% in the non-pCMS group, p < 0.001), right DN (83.0% vs 40.3%, p < 0.001), left superior cerebellar peduncle (SCP) (74.5% vs 27.3%, p < 0.001), right SCP (63.8% vs 23.4%, p < 0.001), left middle cerebellar peduncle (MCP) (51.1% vs 26.0%, p = 0.008), and right MCP (61.7% vs 26.0%, p < 0.001); male sex (83.0% vs 45.5%, p < 0.001); vermis 3 impairment (49.4% vs 19.1%, p = 0.002); solid tumor (91.5% vs 72.7%, p = 0.022); and hydrocephalus (72.3% vs 45.5%, p = 0.006) were more frequent in the pCMS group than in the non-pCMS group. Multivariable logistic analysis showed that male sex (adjusted OR 4.08, p = 0.010) and the cerebro-cerebellar circuit score of T2-weighted images (adjusted OR 2.15, p < 0.001) were independent risk factors for pCMS. The cerebro-cerebellar circuit score positively correlated with the duration of mutism. In Cox regression analysis, the cerebro-cerebellar integrated circuit injury score of T2 (adjusted HR 0.790, 95% CI 0.637-0.980; p = 0.032) and injury of vermis 3 (adjusted HR 3.005, 95% CI 1.197-7.547; p = 0.019) were independently associated with the duration of mutism.

CONCLUSIONS:

Male sex and cerebro-cerebellar circuit damage are independent risk factors for pCMS. The cerebro-cerebellar circuit score indicates the duration of mutism.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cerebelosas / Neoplasias Cerebelosas / Meduloblastoma / Mutismo Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Revista: J Neurosurg Pediatr Asunto de la revista: NEUROCIRURGIA / PEDIATRIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cerebelosas / Neoplasias Cerebelosas / Meduloblastoma / Mutismo Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Revista: J Neurosurg Pediatr Asunto de la revista: NEUROCIRURGIA / PEDIATRIA Año: 2022 Tipo del documento: Article