Chiari I malformation in the very young child: The spectrum of presentations and experience in 31 children under age 6 years

被引:114
作者
Greenlee, JDW [1 ]
Donovan, KA [1 ]
Hasan, DM [1 ]
Menezes, AH [1 ]
机构
[1] Univ Iowa, Hosp & Clin, Dept Neurosurg, Iowa City, IA 52242 USA
关键词
Chiari malformation; headache; dysphagia; pediatric; scoliosis; syringomyelia;
D O I
10.1542/peds.110.6.1212
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction. The entity of hindbrain herniation without myelodysplasia in the very young child has been poorly described. A retrospective analysis of children diagnosed with Chiari I malformation (CM I) before their sixth birthday is presented. Methods. Since 1985,31 children with CM 1 (0.3-5.8) years of age have been diagnosed at University of Iowa Hospitals and Clinics. Their records were reviewed for presenting symptoms, signs, radiographic findings, treatment, complications, and outcome. Results. The average age at diagnosis was 3.3 years. Sixteen patients were under age 3. Chief presenting complaints included impaired oropharyngeal function (35%), scoliosis (23%), headache or neck pain (23%), sensory disturbance (6%), weakness (3%), and other (10%). Sixty-nine percent of children under age 3 had abnormal oropharyngeal function. Three patients under age 3 (19%) had undergone fundoplication and/or gastrostomy before diagnosis of CM I. Common physical findings included abnormal tendon reflexes (68%), scoliosis (26%), abnormal gag reflex (13%), and normal examination (13%). Vocal cord dysfunction (26%, all under age 3) and syringohydromyelia (52%) were also seen. Twenty-five patients were treated surgically at our institution with posterior fossa decompression, duraplasty, and cerebellar tonsillar shrinkage. Three patients were lost to follow-up. Ninety-one percent of patients reported improved symptomatology at last follow-up (mean: 3.9 years). Three patients required reoperation for recurrence of symptoms. Syringomyelia improved in all patients. Scoliosis resolved in 2 of 8 patients, improved in 5, and stabilized in 1. There was no permanent morbidity from surgery. Discussion. We show that children with Chiari I abnormality are very likely to present with oropharyngeal dysfunction if under age 3, and either scoliosis or headache or neck pain worsened by valsalva if age 3 to 5. These symptoms are very likely to improve after Chiari decompression, which can be done with low morbidity. Conclusions. Very young children presenting with oropharyngeal dysfunction, pain worsened by valsalva, or scoliosis should prompt the clinician to consider CM I as a possible cause.
引用
收藏
页码:1212 / 1219
页数:8
相关论文
共 45 条
[1]   SCOLIOSIS ASSOCIATED WITH SYRINGOMYELIA [J].
ARAI, S ;
OHTSUKA, Y ;
MORIYA, H ;
KITAHARA, H ;
MINAMI, S .
SPINE, 1993, 18 (12) :1591-1592
[2]  
BARKOVICH AJ, 1986, AM J NEURORADIOL, V7, P795
[4]   SYMPTOMATIC ARNOLD-CHIARI MALFORMATION - REVIEW OF EXPERIENCE WITH 22 CASES [J].
BELL, WO ;
CHARNEY, EB ;
BRUCE, DA ;
SUTTON, LN ;
SCHUT, L .
JOURNAL OF NEUROSURGERY, 1987, 66 (06) :812-816
[5]  
Cai C, 1997, Semin Pediatr Neurol, V4, P179, DOI 10.1016/S1071-9091(97)80036-8
[6]  
Chang Chih-Zen, 1999, Kaohsiung Journal of Medical Sciences, V15, P659
[7]   Airway abnormalities in patients with Arnold-Chiari malformation [J].
Choi, SS ;
Tran, LP ;
Zalzal, GH .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1999, 121 (06) :720-724
[8]   SYMPTOMATIC CHIARI-I MALFORMATION IN CHILDHOOD - A REPORT OF 7 CASES [J].
DAUSER, RC ;
DIPIETRO, MA ;
VENES, JL .
PEDIATRIC NEUROSCIENCE, 1988, 14 (04) :184-190
[9]   Posterior fossa decompression in syringomyelia associated with a Chiari malformation: a retrospective analysis of 22 patients [J].
Depreitere, B ;
Van Calenbergh, F ;
van Loon, J ;
Goffin, J ;
Plets, C .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2000, 102 (02) :91-96
[10]   CHIARI TYPE-I MALFORMATION IN CHILDREN [J].
DURE, LS ;
PERCY, AK ;
CHEEK, WR ;
LAURENT, JP .
JOURNAL OF PEDIATRICS, 1989, 115 (04) :573-576