PEDIATRICS · 2002 · 190 citations · 36 references
MedicinePediatricsPediatric NeurologyPediatric OrthopaedicsPediatric Plastic SurgeryChiari MalformationCongenital Cranial AnomaliesCongenital Malformation PathologyPediatric DysphagiaChiari Malformation Type ICongenital Cranial MalformationsGastrostomy PlacementPediatric Chiari MalformationSymptomatic Chiari Malformation
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 I (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.
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Chiari I malformations: clinical and radiologic reappraisal.
A.D. Elster, M Y Chen · Radiology · 1992 · 515 citations
Significance of cerebellar tonsillar position on MR
A J Barkovich, Franz J. Wippold, J L Sherman et al. · American Journal of Neuroradiology · 2024 · 438 citations · Full text
Medicine, Neurology, Neurosurgery +13
Variance of the position of the cerebellar tonsils with age: preliminary report.
David J. Mikulis, Orlando Díaz, T K Egglin et al. · Radiology · 1992 · 226 citations