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

被引:130
作者
Catsman-Berrevoets, CE
Van Dongen, HR
Mulder, PGH
Geuze, DPY
Paquier, PF
Lequin, MH
机构
[1] Univ Rotterdam Hosp, Sophia Childrens Hosp, Dept Child Neurol, NL-3000 CB Rotterdam, Netherlands
[2] Univ Rotterdam Hosp, Sophia Childrens Hosp, Dept Child Neurosurg, NL-3000 CB Rotterdam, Netherlands
[3] Univ Rotterdam Hosp, Sophia Childrens Hosp, Dept Child Radiol, NL-3000 CB Rotterdam, Netherlands
[4] Erasmus Univ, Dept Epidemiol & Biostat, NL-3000 DR Rotterdam, Netherlands
[5] Univ Antwerp, Sch Med, Dept Ear Nose & Throat Surg, B-2020 Antwerp, Belgium
[6] Erasme Univ Hosp, Dept Neurol, B-1070 Brussels, Belgium
关键词
mutism and subsequent dysarthria; cerebellar tumour; risk factors;
D O I
10.1136/jnnp.67.6.755
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective-"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. Methods-In a consecutive series of 42 children with a cerebellar tumour, speech and neuroradiological studies (CT and MRT) were systematically analysed preoperatively and postoperatively. Speech was assessed using the Mayo Clinic Lists and the severity of dysarthria using the Michigan rating scale. Results-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. Conclusion-MSD often occurs after paediatric cerebellar tumour removal and is most likely after removal of a medulloblastoma with a maximum lesion diameter>5 cm.
引用
收藏
页码:755 / 757
页数:3
相关论文
共 26 条
  • [1] TRANSIENT MUTISM FOLLOWING A POSTERIOR-FOSSA APPROACH TO CEREBELLAR TUMORS IN CHILDREN - A CRITICAL-REVIEW OF THE LITERATURE
    AGUIAR, PH
    PLESE, JPP
    CIQUINI, O
    MARINE, R
    [J]. CHILDS NERVOUS SYSTEM, 1995, 11 (05) : 306 - 310
  • [2] BAK E, 1983, DEV MED CHILD NEUROL, V25, P81
  • [3] CATSMANBERREVOETS CE, 1992, DEV MED CHILD NEUROL, V34, P1102
  • [4] POSTOPERATIVE MUTISM IN NEUROSURGERY - REPORT OF 2 CASES
    CRUTCHFIELD, JS
    SAWAYA, R
    MEYERS, CA
    MOORE, BD
    [J]. JOURNAL OF NEUROSURGERY, 1994, 81 (01) : 115 - 121
  • [5] THE PATHOPHYSIOLOGY OF ORAL PHARYNGEAL APRAXIA AND MUTISM FOLLOWING POSTERIOR-FOSSA TUMOR RESECTION IN CHILDREN
    DAILEY, AT
    MCKHANN, GM
    BERGER, MS
    [J]. JOURNAL OF NEUROSURGERY, 1995, 83 (03) : 467 - 475
  • [6] DIFFERENTIAL DIAGNOSTIC PATTERNS OF DYSARTHRIA
    DARLEY, FL
    ARONSON, AE
    BROWN, JR
    [J]. JOURNAL OF SPEECH AND HEARING RESEARCH, 1969, 12 (02): : 246 - &
  • [7] Cerebellar mutism: Report of two unusual cases and review of the literature
    Ersahin, Y
    Mutluer, S
    Saydam, S
    Barcin, E
    [J]. CLINICAL NEUROLOGY AND NEUROSURGERY, 1997, 99 (02) : 130 - 134
  • [8] MUTISM AFTER POSTERIOR-FOSSA SURGERY IN CHILDREN - REPORT OF 3 CASES
    FERRANTE, L
    MASTRONARDI, L
    ACQUI, M
    FORTUNA, A
    [J]. JOURNAL OF NEUROSURGERY, 1990, 72 (06) : 959 - 963
  • [9] FRAIOLI B, 1975, APPL NEUROPHYSIOL, V38, P81
  • [10] Halperin EC, 1996, CANCER, V78, P874, DOI 10.1002/(SICI)1097-0142(19960815)78:4<874::AID-CNCR26>3.0.CO