Literature DB >> 18759599

The natural history of the Chiari Type I anomaly.

Federica Novegno1, Massimo Caldarelli, Antonio Massa, Daniela Chieffo, Luca Massimi, Benedetta Pettorini, Gianpiero Tamburrini, Concezio Di Rocco.   

Abstract

OBJECT: Since the advent of MR imaging, an increasing number of asymptomatic or oligosymptomatic patients have been diagnosed with Chiari malformation Type I (CM-I). The decision of whether or not to operate is more difficult in these patients than in those with clear symptoms because of the lack of information about the natural course of this disease.
METHODS: The authors report on their experience in a series of 22 patients with CM-I who were evaluated at the authors' institution, and for whom a conservative approach to treatment was adopted. The patients ranged in age from 1 to 16 years (mean 6.3 years) at diagnosis. Neuroradiological and complete clinical examinations were performed in all patients 6 months after the first observation and every year thereafter. The follow-up period ranged from 3 to 19 years (mean 5.9 years).
RESULTS: Chiari malformation Type I was incidentally detected on MR images in 11 of 22 patients. The remaining 11 patients had minimal clinical signs at presentation that were not regarded as necessitating immediate surgical treatment. Seventeen patients (77.3%) showed progressive improvement in their symptoms or remained asymptomatic at the last follow-up whereas 5 patients (22.7%) experienced worsening, which was mild in 2 cases and required surgical correction in the remaining 3 cases. On MR imaging a mild reduction in tonsillar herniation was appreciated in 4 patients (18.18%), with complete spontaneous resolution in 1 of these. In 16 patients, tonsillar herniation remained stable during follow-up.
CONCLUSIONS: The authors' data confirm the common impression that in both asymptomatic and slightly symptomatic patients with CM-I, a conservative approach to treatment should be adopted with periodic clinical and radiological examinations.

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Year:  2008        PMID: 18759599     DOI: 10.3171/PED/2008/2/9/179

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  51 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

2.  The evolution of cerebellar tonsillar herniation after cranial vault remodeling surgery.

Authors:  J Leikola; A Hukki; A Karppinen; L Valanne; V Koljonen
Journal:  Childs Nerv Syst       Date:  2012-06-04       Impact factor: 1.475

3.  Treatment of Chiari type I malformation in children: the experience of Lyon.

Authors:  Carmine Mottolese; Alexandru Szathmari; Emile Simon; Christophe Rousselle; Anne-Claire Ricci-Franchi; M Hermier
Journal:  Neurol Sci       Date:  2011-12       Impact factor: 3.307

4.  Can Chiari malformation negatively affect higher mental functioning in developmental age?

Authors:  Daria Riva; Arianna Usilla; Veronica Saletti; Sivia Esposito; Sara Bulgheroni
Journal:  Neurol Sci       Date:  2011-12       Impact factor: 3.307

5.  Comment to the paper "Posterior fossa decompression and the cerebellum in Chiari type II malformation: a preliminary MRI study".

Authors:  Mehmet Selcuki
Journal:  Childs Nerv Syst       Date:  2010-12-24       Impact factor: 1.475

6.  Cardiac-Related Spinal Cord Tissue Motion at the Foramen Magnum is Increased in Patients with Type I Chiari Malformation and Decreases Postdecompression Surgery.

Authors:  Braden J Lawrence; Mark Luciano; John Tew; Richard G Ellenbogen; John N Oshinski; Francis Loth; Amanda P Culley; Bryn A Martin
Journal:  World Neurosurg       Date:  2018-05-04       Impact factor: 2.104

7.  Chiari type I and hydrocephalus.

Authors:  Luca Massimi; Giovanni Pennisi; Paolo Frassanito; Gianpiero Tamburrini; Concezio Di Rocco; Massimo Caldarelli
Journal:  Childs Nerv Syst       Date:  2019-06-21       Impact factor: 1.475

8.  Amelioration of Chiari type 1 malformation and syringomyelia following posterior calvarial distraction in Crouzon's syndrome--a case report.

Authors:  Fateh Ahmad; Martin Evans; Nicholas White; Hiroshi Nishikawa; Stephen Dover; Guirish Solanki; Desiderio Rodrigues
Journal:  Childs Nerv Syst       Date:  2013-06-19       Impact factor: 1.475

9.  The incidence of Chiari malformation in nonsyndromic, single suture craniosynostosis.

Authors:  Junnu Leikola; Virve Koljonen; Leena Valanne; Jyri Hukki
Journal:  Childs Nerv Syst       Date:  2009-12-16       Impact factor: 1.475

10.  Role of "major" and "minor" lambdoid arch sutures in posterior cranial fossa changes: mechanism of cerebellar tonsillar herniation in infants with multisutural craniosynostosis.

Authors:  Rosalinda Calandrelli; Gabriella D'Apolito; Marco Panfili; Luca Massimi; Massimo Caldarelli; Cesare Colosimo
Journal:  Childs Nerv Syst       Date:  2015-11-16       Impact factor: 1.475

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