Literature DB >> 20013282

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

Junnu Leikola1, Virve Koljonen, Leena Valanne, Jyri Hukki.   

Abstract

INTRODUCTION: This study was designed to determine the incidence of Chiari malformation (CM) in nonsyndromic single suture craniosynostosis (N-SSSC).
MATERIALS AND METHODS: A retrospective analysis of brain magnetic resonance imaging (MRI) studies of children undergoing craniofacial surgery during 1 January, 2004-31 March, 2009 in Cleft Palate and Craniofacial Centre, Department of Plastic Surgery, Helsinki University Hospital, Helsinki, Finland, was conducted. RESULTS AND DISCUSSION: One hundred twenty-four N-SSSC patients were imaged using brain MRI. Of these 124 patients, seven patients were diagnosed with N-SSSC with an associated CM; the incidence CM in association with N-SSSC was thus 5.6%. The average age at the time of MRI was 37.7 months. All were males, except one. Only two types of synostosis were identified in this patient cohort: synostosis involving the sagittal suture in five cases and right coronal synostosis in two cases. The CM malformations were relatively large. The tonsillar herniation varied from 6 to 12 mm (median 9 mm). All these patients were asymptomatic of their CMs. None had operation designed directly to correct the CM.
CONCLUSION: As a conclusion, we state that the association of CM and N-SSSC is a relatively common finding, with an incidence of 5.6% in preoperative brain MRI. The significance of finding CM in preoperative brain MRI should be assessed individually in asymptomatic patients.

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Year:  2009        PMID: 20013282     DOI: 10.1007/s00381-009-1044-y

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  12 in total

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Review 4.  Chiari malformation in craniosynostosis.

Authors:  Giuseppe Cinalli; Pietro Spennato; Christian Sainte-Rose; Eric Arnaud; Ferdinando Aliberti; Francis Brunelle; Emilio Cianciulli; Dominique Renier
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6.  Posterior cranial fossa volume in patients with rickets: insights into the increased occurrence of Chiari I malformation in metabolic bone disease.

Authors:  R Shane Tubbs; Daniel Webb; Hussein Abdullatif; Michael Conklin; Scott Doyle; W Jerry Oakes
Journal:  Neurosurgery       Date:  2004-08       Impact factor: 4.654

7.  Posterior cranial fossa dimensions in the Chiari I malformation: relation to pathogenesis and clinical presentation.

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Review 8.  Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review.

Authors:  Charles Raybaud; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2007-09-20       Impact factor: 1.475

9.  The natural history of the Chiari Type I anomaly.

Authors:  Federica Novegno; Massimo Caldarelli; Antonio Massa; Daniela Chieffo; Luca Massimi; Benedetta Pettorini; Gianpiero Tamburrini; Concezio Di Rocco
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10.  Sagittal synostosis in X-linked hypophosphatemic rickets and related diseases.

Authors:  Guido Currarino
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  11 in total

1.  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

2.  Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial development.

Authors:  Elisa Merello; Lorenzo Tattini; Alberto Magi; Andrea Accogli; Gianluca Piatelli; Marco Pavanello; Domenico Tortora; Armando Cama; Zoha Kibar; Valeria Capra; Patrizia De Marco
Journal:  Eur J Hum Genet       Date:  2017-05-17       Impact factor: 4.246

Review 3.  Tonsillar herniation spectrum: more than just Chiari I. Update and controversies on classification and management.

Authors:  Pietro Fiaschi; Giovanni Morana; Pasquale Anania; Andrea Rossi; Alessandro Consales; Gianluca Piatelli; Armando Cama; Marco Pavanello
Journal:  Neurosurg Rev       Date:  2019-11-10       Impact factor: 3.042

4.  Chiari 1 malformation and untreated sagittal synostosis: a new subset of complex Chiari?

Authors:  Laura Grazia Valentini; Veronica Saletti; Alessandra Erbetta; Luisa Chiapparini; Marika Furlanetto
Journal:  Childs Nerv Syst       Date:  2019-07-21       Impact factor: 1.475

5.  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

Review 6.  Contemporary occurrence of hydrocephalus and Chiari I malformation in sagittal craniosynostosis. Case report and review of the literature.

Authors:  Francesco Giovanni Sgulò; Pietro Spennato; Ferdinando Aliberti; Giuliana Di Martino; Daniele Cascone; Giuseppe Cinalli
Journal:  Childs Nerv Syst       Date:  2016-07-22       Impact factor: 1.475

7.  Adult Chiari Type 1 Malformation with Holocord Syringomyelia Associated with Sagittal Synostosis.

Authors:  Masakazu Sano; Junichi Yoshimura; Yukihiko Fujii
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Review 8.  Functional and morphological changes in hypoplasic posterior fossa.

Authors:  Federico Bianchi; Alberto Benato; Paolo Frassanito; Gianpiero Tamburrini; Luca Massimi
Journal:  Childs Nerv Syst       Date:  2021-06-25       Impact factor: 1.475

9.  Chiari Type I malformation yielded to the diagnosis of Crouzon syndrome.

Authors:  Aydin Canpolat; Mehmet Osman Akçakaya; Emre Altunrende; Harun Mehmet Ozlü; Hakan Duman; Tuğrul Ton; Osman Akdemir
Journal:  J Neurosci Rural Pract       Date:  2014-01

Review 10.  Craniosynostosis in Growing Children : Pathophysiological Changes and Neurosurgical Problems.

Authors:  Jung Won Choi; So Young Lim; Hyung-Jin Shin
Journal:  J Korean Neurosurg Soc       Date:  2016-05-10
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