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      Neuroimaging of pediatric tumors of the sellar region—A review in light of the 2021 WHO classification of tumors of the central nervous system

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          Abstract

          Sellar/suprasellar tumors comprise about 10% of all pediatric Central Nervous System (CNS) tumors and include a wide variety of entities, with different cellular origins and distinctive histological and radiological findings, demanding customized neuroimaging protocols for appropriate diagnosis and management. The 5th edition of the World Health Organization (WHO) classification of CNS tumors unprecedently incorporated both histologic and molecular alterations into a common diagnostic framework, with a great impact in tumor classification and grading. Based on the current understanding of the clinical, molecular, and morphological features of CNS neoplasms, there have been additions of new tumor types and modifications of existing ones in the latest WHO tumor classification. In the specific case of sellar/suprasellar tumors, changes include for example separation of adamantinomatous and papillary craniopharyngiomas, now classified as distinct tumor types. Nevertheless, although the current molecular landscape is the fundamental driving force to the new WHO CNS tumor classification, the imaging profile of sellar/suprasellar tumors remains largely unexplored, particularly in the pediatric population. In this review, we aim to provide an essential pathological update to better understand the way sellar/suprasellar tumors are currently classified, with a focus on the pediatric population. Furthermore, we intend to present the neuroimaging features that may assist in the differential diagnosis, surgical planning, adjuvant/neoadjuvant therapy, and follow-up of this group of tumors in children.

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          Cancer Statistics, 2021

          Each year, the American Cancer Society estimates the numbers of new cancer cases and deaths in the United States and compiles the most recent data on population-based cancer occurrence. Incidence data (through 2017) were collected by the Surveillance, Epidemiology, and End Results Program; the National Program of Cancer Registries; and the North American Association of Central Cancer Registries. Mortality data (through 2018) were collected by the National Center for Health Statistics. In 2021, 1,898,160 new cancer cases and 608,570 cancer deaths are projected to occur in the United States. After increasing for most of the 20th century, the cancer death rate has fallen continuously from its peak in 1991 through 2018, for a total decline of 31%, because of reductions in smoking and improvements in early detection and treatment. This translates to 3.2 million fewer cancer deaths than would have occurred if peak rates had persisted. Long-term declines in mortality for the 4 leading cancers have halted for prostate cancer and slowed for breast and colorectal cancers, but accelerated for lung cancer, which accounted for almost one-half of the total mortality decline from 2014 to 2018. The pace of the annual decline in lung cancer mortality doubled from 3.1% during 2009 through 2013 to 5.5% during 2014 through 2018 in men, from 1.8% to 4.4% in women, and from 2.4% to 5% overall. This trend coincides with steady declines in incidence (2.2%-2.3%) but rapid gains in survival specifically for nonsmall cell lung cancer (NSCLC). For example, NSCLC 2-year relative survival increased from 34% for persons diagnosed during 2009 through 2010 to 42% during 2015 through 2016, including absolute increases of 5% to 6% for every stage of diagnosis; survival for small cell lung cancer remained at 14% to 15%. Improved treatment accelerated progress against lung cancer and drove a record drop in overall cancer mortality, despite slowing momentum for other common cancers.
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            The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.

            The 2016 World Health Organization Classification of Tumors of the Central Nervous System is both a conceptual and practical advance over its 2007 predecessor. For the first time, the WHO classification of CNS tumors uses molecular parameters in addition to histology to define many tumor entities, thus formulating a concept for how CNS tumor diagnoses should be structured in the molecular era. As such, the 2016 CNS WHO presents major restructuring of the diffuse gliomas, medulloblastomas and other embryonal tumors, and incorporates new entities that are defined by both histology and molecular features, including glioblastoma, IDH-wildtype and glioblastoma, IDH-mutant; diffuse midline glioma, H3 K27M-mutant; RELA fusion-positive ependymoma; medulloblastoma, WNT-activated and medulloblastoma, SHH-activated; and embryonal tumour with multilayered rosettes, C19MC-altered. The 2016 edition has added newly recognized neoplasms, and has deleted some entities, variants and patterns that no longer have diagnostic and/or biological relevance. Other notable changes include the addition of brain invasion as a criterion for atypical meningioma and the introduction of a soft tissue-type grading system for the now combined entity of solitary fibrous tumor / hemangiopericytoma-a departure from the manner by which other CNS tumors are graded. Overall, it is hoped that the 2016 CNS WHO will facilitate clinical, experimental and epidemiological studies that will lead to improvements in the lives of patients with brain tumors.
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              The 2021 WHO Classification of Tumors of the Central Nervous System: a summary

              The fifth edition of the WHO Classification of Tumors of the Central Nervous System (CNS), published in 2021, is the sixth version of the international standard for the classification of brain and spinal cord tumors. Building on the 2016 updated fourth edition and the work of the Consortium to Inform Molecular and Practical Approaches to CNS Tumor Taxonomy, the 2021 fifth edition introduces major changes that advance the role of molecular diagnostics in CNS tumor classification. At the same time, it remains wedded to other established approaches to tumor diagnosis such as histology and immunohistochemistry. In doing so, the fifth edition establishes some different approaches to both CNS tumor nomenclature and grading and it emphasizes the importance of integrated diagnoses and layered reports. New tumor types and subtypes are introduced, some based on novel diagnostic technologies such as DNA methylome profiling. The present review summarizes the major general changes in the 2021 fifth edition classification and the specific changes in each taxonomic category. It is hoped that this summary provides an overview to facilitate more in-depth exploration of the entire fifth edition of the WHO Classification of Tumors of the Central Nervous System.
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                Author and article information

                Contributors
                Journal
                Front Pediatr
                Front Pediatr
                Front. Pediatr.
                Frontiers in Pediatrics
                Frontiers Media S.A.
                2296-2360
                21 June 2023
                2023
                : 11
                : 1162654
                Affiliations
                [ 1 ]Department of Neuroradiology, Centro Hospitalar Universitário São João , Porto, Portugal
                [ 2 ]Diagnostic Neuroradiology Unit, Imaging Department, Centro Hospitalar Vila Nova de Gaia/Espinho , Vila Nova de Gaia, Portugal
                [ 3 ]Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho , Braga, Portugal
                [ 4 ]Faculty of Medicine, University of Lisbon , Lisbon, Portugal
                [ 5 ]Faculty of Medicine, University of Porto , Porto, Portugal
                [ 6 ]Neuroradiology Unit, IRCCS Istituto Giannina Gaslini , Genoa, Italy
                [ 7 ]Department of Health Sciences (DISSAL), University of Genoa , Genoa, Italy
                Author notes

                Edited by: Fabrício Guimarães Gonçalves, Childrens Hospital of Philadelphia, United States

                Reviewed by: Flavio Giordano, University of Florence, Italy Joseph Louis Lasky, Cure 4 The Kids, United States Cesar Augusto Alves, Childrens Hospital of Philadelphia, United States

                [* ] Correspondence: Ana Filipa Geraldo anafilipageraldo@ 123456gmail.com

                Abbreviations ACP, Adamantinomatous craniopharyngioma; ACTH, Adrenocorticotropic hormone; ADC, Apparent diffusion coefficient; AT/RT, Atypical teratoid/rhabdoid tumor; β-HCG, Beta-human chorionic gonadotropin; CBF, Cerebral blood flow; CISS, Constructive interference in steady state; CNS, Central nervous system; CT, computed tomography; DCEI, Dynamic contrast-enhanced imaging; ECD, Erdheim-Chester Disease; DRIVE, Driven equilibrium radio frequency reset pulse; DWI, Diffusion weighted imaging; FIESTA, Fast imaging employing steady-state acquisition; FLAIR, Fluid attenuated inversion recovery; GCT, Germ cell tumors; JXG, Juvenile xanthogranuloma; LCH, Langerhans cell histiocytosis; MEN-1, Multiple endocrine neoplasia type 1; MRI, magnetic resonance imaging; NF1, Neurofibromatosis type 1; OPG, Optic pathway glioma; PCP, papillary craniopharyngioma; PitNET- Pituitary neuroendocrine tumor; RCC, Rathke's cleft cyst; SCO, Spindle cell oncocytoma; SPACE, Sampling perfection with application optimized contrast using different flip angle evolution; SWI, Susceptibility weighted imaging, WHO- World Health Organization.

                Article
                10.3389/fped.2023.1162654
                10320298
                37416813
                e38b6edb-ffca-4dcd-8d77-ff4aab974b9b
                © 2023 Maia, Miranda, Geraldo, Sampaio, Ramaglia, Tortora, Severino and Rossi.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 09 February 2023
                : 07 June 2023
                Page count
                Figures: 12, Tables: 2, Equations: 0, References: 175, Pages: 0, Words: 0
                Categories
                Pediatrics
                Review
                Custom metadata
                Pediatric Neurology

                neuroimaging,pediatric tumors,suprasellar and sellar,cns tumors,who classification

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