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Tumour type and size are high risk factors for the syndrome of "cerebellar" mutism and subsequent dysarthria.

Authors :
Catsman-Berrevoets CE
Van Dongen HR
Mulder PGH
Geuze DP
Paquier PF
Lequin MH
Catsman-Berrevoets, C E
Van Dongen, H R
Mulder, P G
Paz y Geuze, D
Paquier, P F
Lequin, M H
Source :
Journal of Neurology, Neurosurgery & Psychiatry; Dec1999, p755-757, 3p
Publication Year :
1999

Abstract

<bold>Objective: </bold>"Cerebellar mutis" and subsequent dysarthria (MSD) is a documented complication of posterior fossa surgery in children. In this prospective study the following risk factors for MSD were assessed: type, size and site of the tumour; hydrocephalus at presentation and after surgery, cerebellar incision site, postoperative infection, and cerebellar swelling.<bold>Methods: </bold>In a consecutive series of 42 children with a cerebellar tumour, speech and neuroradiological studies (CT and MRI) were systematically analysed preoperatively and postoperatively. Speech was assessed using the Mayo Clinic lists and the severity of dysarthria using the Michigan rating scale.<bold>Results: </bold>Twelve children (29%) developed MSD postoperatively. The type of tumour, midline localisation, and vermal incision were significant single independent risk factors. In addition, an interdependency of possible risk factors (tumour>5 cm, medulloblastoma) was found.<bold>Conclusion: </bold>MSD often occurs after paediatric cerebellar tumour removal and is most likely after removal of a medulloblastoma with a maximum lesion diameter>5 cm. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00223050
Database :
Complementary Index
Journal :
Journal of Neurology, Neurosurgery & Psychiatry
Publication Type :
Academic Journal
Accession number :
107090038