Midline developmental abnormalities of the posterior fossa: Correlation of classification with outcome

被引:26
作者
Domingo, Z [1 ]
Peter, J [1 ]
机构
[1] UNIV CAPE TOWN,RED CROSS WAR MEM CHILDRENS HOSP,DEPT PAEDIAT NEUROSURG,CAPE TOWN,SOUTH AFRICA
关键词
arachnoid cysts; cystoperitoneal shunt; Dandy-Walker syndrome; posterior fossa cysts;
D O I
10.1159/000121026
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Fifty children with developmental retrocerebellar cysts of the posterior fossa, treated over an 11-year period, were assessed. The cysts were classified according to a morphological classification based on axial computerized tomography scans in order to assess the usefulness of this classification with regard to treatment and outcome. There were 35 patients with the Dandy-Walker complex and 15 patients with posterior fossa cysts. All surgically treated patients had cerebrospinal fluid shunting as the only form of treatment. Cystoperitoneal shunts were the treatment of choice. Although the morphological classification has relevance with regard to the embryological development of the cyst, it does not influence the selection of treatment nor the surgical outcome following shunt insertion.
引用
收藏
页码:111 / 118
页数:8
相关论文
共 38 条
[1]   DANDY-WALKER SYNDROME - POSTERIOR-FOSSA CRANIECTOMY AND CYST FENESTRATION AFTER SEVERAL SHUNT REVISIONS [J].
ALMEIDA, GM ;
MATUSHITA, H ;
MATTOSINHOFRANCA, LC ;
SHIBATA, MK .
CHILDS NERVOUS SYSTEM, 1990, 6 (06) :335-337
[2]  
ALTMAN NR, 1992, AM J NEURORADIOL, V13, P691
[3]  
[Anonymous], 1887, BRAIN, DOI [DOI 10.1093/BRAIN/9.3.352, 10.1093/brain/9.3.352]
[4]   POSTERIOR-FOSSA CYSTS - CLINICAL, NEURORADIOLOGICAL AND SURGICAL FEATURES [J].
ARAI, H ;
SATO, K .
CHILDS NERVOUS SYSTEM, 1991, 7 (03) :156-164
[5]   DANDY-WALKER SYNDROME - EXPERIENCE AT THE HOSPITAL FOR SICK CHILDREN, TORONTO [J].
ASAI, A ;
HOFFMAN, HJ ;
HENDRICK, EB ;
HUMPHREYS, RP .
PEDIATRIC NEUROSCIENCE, 1989, 15 (02) :66-73
[6]  
BARKOVICH AJ, 1989, AM J NEURORADIOL, V10, P977
[8]   OCCIPITAL MENINGOCELES IN PATIENTS WITH THE DANDY-WALKER SYNDROME [J].
BINDAL, AK ;
STORRS, BB ;
MCLONE, DG .
NEUROSURGERY, 1991, 28 (06) :844-847
[9]   JOUBERT SYNDROME - EPISODIC HYPERPNEA, ABNORMAL EYE-MOVEMENTS, RETARDATION AND ATAXIA, ASSOCIATED WITH DYSPLASIA OF CEREBELLAR VERMIS [J].
BOLTSHAUSER, E ;
ISLER, W .
NEUROPADIATRIE, 1977, 8 (01) :57-66
[10]   A FAMILY WITH 3 RECESSIVE TRAITS AND HOMOZYGOSITY FOR A LONG 9QH+ CHROMOSOME SEGMENT [J].
CHRISTIAN, JC ;
DEXTER, RN ;
PALMER, CG ;
MULLER, J .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 6 (04) :301-308