A 78‐year‐old woman with diffuse white matter infiltration and predominant involvement of bilateral temporo‐parieto‐occipital regions

Author:

Paoli Charlotte1,Mc Leer Anne2,Boyer Julien3,Mondot Lydiane4,Dadone‐Montaudié Bérengère5,Godfraind Catherine6,Burel‐Vandenbos Fanny1ORCID

Affiliation:

1. Laboratoire Central d'Anatomie Pathologique, Department of Pathology and Molecular Oncology University Hospital of Nice, Université Côte d'Azur Nice France

2. Grenoble Alpes University Hospital Pathology Department Institute for Advanced Biosciences UGA/INSERM U1209/CNRS 5309, Grenoble Alpes University Grenoble France

3. Laboratoire d'Anatomie Pathologique Centre de lutte contre le cancer Antoine Lacassagne Nice France

4. Service d'imagerie médicale University Hospital of Nice, Université Côte d'Azur Nice France

5. Laboratoire d'Oncologie moléculaire, Department of Pathology and Molecular Oncology University hospital of Nice, Université Côte d'Azur Nice France

6. Neuropathology Unit University Hospital of Clermont‐Ferrand and University Clermont‐Auvergne, M2iSH UMR1071 Clermont‐Ferrand France

Abstract

AbstractDiffuse paediatric‐type high‐grade glioma, H3‐wildtype and IDH‐wildtype (H3/IDH‐wt‐pHGG) is a newly defined entity amongst brain tumours, primarily reported in children. It is a rare, ill‐defined type of tumour and the only method to diagnose it is DNA methylation profiling. The case we report here carries new knowledge about this tumour which may, in fact, occur in elderly patients, be devoid of evocative genomic abnormalities reported in children and harbour a misleading mutation.

Publisher

Wiley

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