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Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?

作者信息

d'Amati Antonio, Bargiacchi Lavinia, Rossi Sabrina, Carai Andrea, Bertero Luca, Barresi Valeria, Errico Maria Elena, Buccoliero Anna Maria, Asioli Sofia, Marucci Gianluca, Del Baldo Giada, Mastronuzzi Angela, Miele Evelina, D'Antonio Federica, Schiavello Elisabetta, Biassoni Veronica, Massimino Maura, Gessi Marco, Antonelli Manila, Gianno Francesca

机构信息

Unit of Anatomical Pathology, Department of Precision and Regenerative Medicine and Ionian Area, University of Bari "Aldo Moro", Bari, Italy.

Unit of Human Anatomy and Histology, Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Bari "Aldo Moro", Bari, Italy.

出版信息

Front Mol Neurosci. 2024 Mar 13;17:1268038. doi: 10.3389/fnmol.2024.1268038. eCollection 2024.


DOI:10.3389/fnmol.2024.1268038
PMID:38544524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10966132/
Abstract

The fifth edition of the WHO Classification of Tumors of the Central Nervous System (CNS), published in 2021, established new approaches to both CNS tumor nomenclature and grading, emphasizing the importance of integrated diagnoses and layered reports. This edition increased the role of molecular diagnostics in CNS tumor classification while still relying on other established approaches such as histology and immunohistochemistry. Moreover, it introduced new tumor types and subtypes based on novel diagnostic technologies such as DNA methylome profiling. Over the past decade, molecular techniques identified numerous key genetic alterations in CSN tumors, with important implications regarding the understanding of pathogenesis but also for prognosis and the development and application of effective molecularly targeted therapies. This review summarizes the major changes in the 2021 fifth edition classification of pediatric CNS tumors, highlighting for each entity the molecular alterations and other information that are relevant for diagnostic, prognostic, or therapeutic purposes and that patients' and oncologists' need from a pathology report.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be05/10966132/6849a6d8a3e2/fnmol-17-1268038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be05/10966132/6849a6d8a3e2/fnmol-17-1268038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be05/10966132/6849a6d8a3e2/fnmol-17-1268038-g001.jpg

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Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?

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[3]
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[4]
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本文引用的文献

[1]
Unlocking the power of precision medicine for pediatric low-grade gliomas: molecular characterization for targeted therapies with enhanced safety and efficacy.

Front Oncol. 2023-6-15

[2]
Intracranial mesenchymal tumor with (novel) COX14::PTEN rearrangement.

Acta Neuropathol Commun. 2023-6-13

[3]
Group-specific cellular metabolism in Medulloblastoma.

J Transl Med. 2023-6-5

[4]
Common molecular features of H3K27M DMGs and PFA ependymomas map to hindbrain developmental pathways.

Acta Neuropathol Commun. 2023-2-9

[5]
Genomic profiling and prognostic factors of H3 K27M-mutant spinal cord diffuse glioma.

Brain Pathol. 2023-7

[6]
Pediatric diffuse midline glioma H3K27- altered: A complex clinical and biological landscape behind a neatly defined tumor type.

Front Oncol. 2023-1-16

[7]
A non-hemispheric transtentorial ZFTA fusion-positive ependymoma in a 6-month-old boy.

Neuropathol Appl Neurobiol. 2023-2

[8]
Tumor Microenvironment and Microvascular Density in Human Glioblastoma.

Cells. 2022-12-20

[9]
Mutations and Pediatric High-Grade Gliomas: A Comparative Genomic Study in Primary and Recurrent Tumors.

Diagnostics (Basel). 2022-12-27

[10]
Early ependymal tumor with MN1-BEND2 fusion: a mostly cerebral tumor of female children with a good prognosis that is distinct from classical astroblastoma.

J Neurooncol. 2023-2

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