A novel radiological classification system for cerebral gliomas: The Brain-Grid.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 21 10 2018
accepted: 09 01 2019
entrez: 25 1 2019
pubmed: 25 1 2019
medline: 8 11 2019
Statut: epublish

Résumé

Standard radiological/topographical classifications of gliomas often do not reflect the real extension of the tumor within the lobar-cortical anatomy. Furthermore, these systems do not provide information on the relationship between tumor growth and the subcortical white matter architecture. We propose the use of an anatomically standardized grid system (the Brain-Grid) to merge serial morphological magnetic resonance imaging (MRI) scans with a representative tractographic atlas. Two illustrative cases are presented to show the potential advantages of this classification system. MRI scans of 39 patients (WHO grade II and III gliomas) were analyzed with a standardized grid created by intersecting longitudinal lines on the axial, sagittal, and coronal planes. The anatomical landmarks were chosen from an average brain, spatially normalized to the Montreal Neurological Institute (MNI) space and the Talairach space. Major white matter pathways were reconstructed with a deterministic tracking algorithm on a reference atlas and analyzed using the Brain-Grid system. In all, 48 brain grid voxels (areas defined by 3 coordinates, axial (A), coronal (C), sagittal (S) and numbers from 1 to 4) were delineated in each MRI sequence and on the tractographic atlas. The number of grid voxels infiltrated was consistent, also in the MNI space. The sub-cortical insula/basal ganglia (A3-C2-S2) and the fronto-insular region (A3-C2-S1) were most frequently involved. The inferior fronto-occipital fasciculus, anterior thalamic radiation, uncinate fasciculus, and external capsule were the most frequently associated pathways in both hemispheres. The Brain-Grid based classification system provides an accurate observational tool in all patients with suspected gliomas, based on the comparison of grid voxels on a morphological MRI and segmented white matter atlas. Important biological information on tumor kinetics including extension, speed, and preferential direction of progression can be observed and even predicted with this system. This novel classification can easily be applied to both prospective and retrospective cohorts of patients and increase our comprehension of glioma behavior.

Identifiants

pubmed: 30677090
doi: 10.1371/journal.pone.0211243
pii: PONE-D-18-30459
pmc: PMC6345500
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0211243

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Francesco Latini (F)

Department of Neuroscience, Neurosurgery, Uppsala University, Uppsala, Sweden.

Markus Fahlström (M)

Department of Surgical Sciences, Radiology, Uppsala University, Uppsala, Sweden.

Shala G Berntsson (SG)

Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.

Elna-Marie Larsson (EM)

Department of Surgical Sciences, Radiology, Uppsala University, Uppsala, Sweden.

Anja Smits (A)

Department of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
Institute of Neuroscience and Physiology, Department of Clinical Neuroscience, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Mats Ryttlefors (M)

Department of Neuroscience, Neurosurgery, Uppsala University, Uppsala, Sweden.

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Classifications MeSH