Literature DB >> 12456921

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

Jeremy D W Greenlee1, Kathleen A Donovan, David M Hasan, Arnold H Menezes.   

Abstract

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.

Entities:  

Mesh:

Year:  2002        PMID: 12456921     DOI: 10.1542/peds.110.6.1212

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  40 in total

Review 1.  Unusual presentation of Chiari I in toddlers: case reports and review of the literature.

Authors:  Caitlin L Carew; Asuri Prasad; Keng Yeow Tay; Sandrine de Ribaupierre
Journal:  Childs Nerv Syst       Date:  2012-06-03       Impact factor: 1.475

Review 2.  Pathogenesis of syringomyelia associated with Chiari type 1 malformation: review of evidences and proposal of a new hypothesis.

Authors:  Izumi Koyanagi; Kiyohiro Houkin
Journal:  Neurosurg Rev       Date:  2010-06-08       Impact factor: 3.042

3.  Histological study of the occipital bone from patients with Chiari I malformation.

Authors:  R Shane Tubbs; Annie Laurie Benzie; Elias Rizk; Joshua J Chern; Marios Loukas; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2015-09-21       Impact factor: 1.475

4.  Arnold Chiari type 1 malformation presenting with sleep disordered breathing in well children.

Authors:  C Murray; C Seton; K Prelog; D A Fitzgerald
Journal:  Arch Dis Child       Date:  2006-04       Impact factor: 3.791

5.  Treatment of Chiari malformation: who, when and how.

Authors:  Alessia Imperato; Vincenzo Seneca; Valentina Cioffi; Giuseppe Colella; Michelangelo Gangemi
Journal:  Neurol Sci       Date:  2011-12       Impact factor: 3.307

6.  The Seow Operative Score (SOS) as a decision-making adjunct for paediatric Chiari I malformation: a preliminary study.

Authors:  Sharon Y Y Low; Lee Ping Ng; Audrey J L Tan; David C Y Low; Wan Tew Seow
Journal:  Childs Nerv Syst       Date:  2019-06-07       Impact factor: 1.475

7.  Arnold Chiari I malformation with tip-toe gait: a case report.

Authors:  Gi Hoon Hwang; Ghi Chan Kim; Ho Joong Jeong; Young-Joo Sim; Yong Seok Park
Journal:  Korean J Spine       Date:  2013-03-31

8.  Neurological pictures in paediatric Chiari I malformation.

Authors:  Veronica Saletti; Silvia Esposito; Manuela Frittoli; Laura Grazia Valentini; Luisa Chiapparini; Sara Bulgheroni; Daria Riva
Journal:  Neurol Sci       Date:  2011-12       Impact factor: 3.307

9.  Clinical Characteristics, Imaging Findings and Surgical Outcomes of Chiari Malformation Type I in Pediatric and Adult Patients.

Authors:  Zhuo-Wei Lei; Shi-Qiang Wu; Zhuo Zhang; Yang Han; Jun-Wen Wang; Feng Li; Kai Shu
Journal:  Curr Med Sci       Date:  2018-04-30

Review 10.  Malformations of the craniocervical junction (Chiari type I and syringomyelia: classification, diagnosis and treatment).

Authors:  Alfredo Avellaneda Fernández; Alberto Isla Guerrero; Maravillas Izquierdo Martínez; María Eugenia Amado Vázquez; Javier Barrón Fernández; Ester Chesa i Octavio; Javier De la Cruz Labrado; Mercedes Escribano Silva; Marta Fernández de Gamboa Fernández de Araoz; Rocío García-Ramos; Miguel García Ribes; Carmen Gómez; Joaquín Insausti Valdivia; Ramón Navarro Valbuena; José R Ramón
Journal:  BMC Musculoskelet Disord       Date:  2009-12-17       Impact factor: 2.362

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