A Critical Update of the Classification of Chiari and Chiari-like Malformations

Author:

Sahuquillo Juan123ORCID,Moncho Dulce24ORCID,Ferré Alex25,López-Bermeo Diego12,Sahuquillo-Muxi Aasma2ORCID,Poca Maria A.123ORCID

Affiliation:

1. Department of Neurosurgery, Vall d’Hebron University Hospital, Passeig Vall d’Hebron 119-129, 08035 Barcelona, Spain

2. Neurotraumatology and Neurosurgery Research Unit, Vall d’Hebron Institut de Recerca (VHIR), Vall d’Hebron Barcelona Hospital Campus, Passeig Vall d’Hebron 119-129, 08035 Barcelona, Spain

3. Department of Surgery, Universitat Autònoma de Barcelona, Bellaterra, 08193 Barcelona, Spain

4. Clinical Neurophysiology Department, Vall d’Hebron Hospital Universitari, Vall d’Hebron Barcelona Hospital Campus, Passeig Vall d’Hebron 119-129, 08035 Barcelona, Spain

5. Sleep Unit, Pneumology Department, Vall d’Hebron Hospital Universitari, Vall d’Hebron Barcelona Hospital Campus, Passeig Vall d’Hebron 119-129, 08035 Barcelona, Spain

Abstract

Chiari malformations are a group of craniovertebral junction anomalies characterized by the herniation of cerebellar tonsils below the foramen magnum, often accompanied by brainstem descent. The existing classification systems for Chiari malformations have expanded from the original four categories to nine, leading to debates about the need for a more descriptive and etiopathogenic terminology. This review aims to examine the various classification approaches employed and proposes a simplified scheme to differentiate between different types of tonsillar herniations. Furthermore, it explores the most appropriate terminology for acquired herniation of cerebellar tonsils and other secondary Chiari-like malformations. Recent advances in magnetic resonance imaging (MRI) have revealed a higher prevalence and incidence of Chiari malformation Type 1 (CM1) and identified similar cerebellar herniations in individuals unrelated to the classic phenotypes described by Chiari. As we reassess the existing classifications, it becomes crucial to establish a terminology that accurately reflects the diverse presentations and underlying causes of these conditions. This paper contributes to the ongoing discussion by offering insights into the evolving understanding of Chiari malformations and proposing a simplified classification and terminology system to enhance diagnosis and management.

Funder

the European Regional Development Fund

the Agència de Gestió d’Ajuts Universitaris i de Recerca (AGAUR), Departament de Recerca i Universitats de la Generalitat de Catalunya, Spain

the Agència de Gestió d’Ajuts Universitaris i de Recerca

Asociación Nacional de Amigos de Arnold-Chiari

Asociación Chiari y Siringomielia del Principado de Asturias

Federación Española de Malformación de Chiari y Patologías Asociadas

Mariana Dañobeitia

Publisher

MDPI AG

Subject

General Medicine

Reference167 articles.

1. Chiari Type 1 Deformity in Children: Pathogenetic, Clinical, Neuroimaging, and Management Aspects;Poretti;Neuropediatrics,2016

2. Chiari I—A ‘not so’ congenital malformation?;Thompson;Childs Nerv. Syst.,2019

3. Chiari, H. (1895). Über Veränderungen des Kleinhirns, des Pons und der Medulla Oblongata in Folge von Congenitaler Hydrocephalie, K.K. Hof- und Staatsdruckerei.

4. Über Veränderungen des Kleinhirns Infolge von Hydrocephalie des Grosshirns;Chiari;Denkschr. Der Kais. Akad. Der Wiss. /Math.-Naturwissenschaftliche Cl.,1891

5. Chiari Malformation: An Unhelpful Eponym;World Neurosurg.,2021

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