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What’s new in the WHO 2022 classification of kidney tumours?
The World Health Organization (WHO) 2022 classification of urinary and male genital tumours (5th edition) has significantly improved our understanding of the morphologic, immunohistochemical, and molecular characteristics of renal tumours. The aim of this review is to outline the most important chan...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Pacini Editore srl
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10342217/ https://www.ncbi.nlm.nih.gov/pubmed/36645398 http://dx.doi.org/10.32074/1591-951X-818 |
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author | Alaghehbandan, Reza Siadat, Farshid Trpkov, Kiril |
author_facet | Alaghehbandan, Reza Siadat, Farshid Trpkov, Kiril |
author_sort | Alaghehbandan, Reza |
collection | PubMed |
description | The World Health Organization (WHO) 2022 classification of urinary and male genital tumours (5th edition) has significantly improved our understanding of the morphologic, immunohistochemical, and molecular characteristics of renal tumours. The aim of this review is to outline the most important changes and diagnostic updates in the WHO 2022 classification of kidney tumours. A major change in this edition is the grouping of renal tumours into broader categories that include “clear cell renal tumours”, “papillary renal tumours”, “oncocytic and chromophobe renal tumours”, “collecting duct tumours” as well as adding two categories of “other renal tumours” and “molecularly defined renal carcinomas”. Novel entities included in the WHO 2022 classification are eosinophilic solid and cystic renal cell carcinoma (ESC RCC), anaplastic lymphoma kinase (ALK)-rearranged RCC and ELOC (formerly TCEB1)-mutated RCC. The category of “other renal tumours” includes a group of diverse, unrelated renal tumours that do not fit into other categories. The group of “molecularly defined renal carcinomas” reflects recent discoveries in the renal tumour genomics. These molecularly-defined renal entities demonstrate a set of morphologic features reflecting genotype-phenotype relationships. Final diagnosis of such entities rests on phenotypic and immunohistochemical (IHC) correlation, usually associated with IHC surrogate makers that reflect specific genetic abnormalities. |
format | Online Article Text |
id | pubmed-10342217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Pacini Editore srl |
record_format | MEDLINE/PubMed |
spelling | pubmed-103422172023-07-14 What’s new in the WHO 2022 classification of kidney tumours? Alaghehbandan, Reza Siadat, Farshid Trpkov, Kiril Pathologica Review The World Health Organization (WHO) 2022 classification of urinary and male genital tumours (5th edition) has significantly improved our understanding of the morphologic, immunohistochemical, and molecular characteristics of renal tumours. The aim of this review is to outline the most important changes and diagnostic updates in the WHO 2022 classification of kidney tumours. A major change in this edition is the grouping of renal tumours into broader categories that include “clear cell renal tumours”, “papillary renal tumours”, “oncocytic and chromophobe renal tumours”, “collecting duct tumours” as well as adding two categories of “other renal tumours” and “molecularly defined renal carcinomas”. Novel entities included in the WHO 2022 classification are eosinophilic solid and cystic renal cell carcinoma (ESC RCC), anaplastic lymphoma kinase (ALK)-rearranged RCC and ELOC (formerly TCEB1)-mutated RCC. The category of “other renal tumours” includes a group of diverse, unrelated renal tumours that do not fit into other categories. The group of “molecularly defined renal carcinomas” reflects recent discoveries in the renal tumour genomics. These molecularly-defined renal entities demonstrate a set of morphologic features reflecting genotype-phenotype relationships. Final diagnosis of such entities rests on phenotypic and immunohistochemical (IHC) correlation, usually associated with IHC surrogate makers that reflect specific genetic abnormalities. Pacini Editore srl 2023-01-16 /pmc/articles/PMC10342217/ /pubmed/36645398 http://dx.doi.org/10.32074/1591-951X-818 Text en © 2023 Copyright by Società Italiana di Anatomia Patologica e Citopatologia Diagnostica, Divisione Italiana della International Academy of Pathology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access journal distributed in accordance with the CC-BY-NC-ND (Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International) license: the work can be used by mentioning the author and the license, but only for non-commercial purposes and only in the original version. For further information: https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en |
spellingShingle | Review Alaghehbandan, Reza Siadat, Farshid Trpkov, Kiril What’s new in the WHO 2022 classification of kidney tumours? |
title | What’s new in the WHO 2022 classification of kidney tumours? |
title_full | What’s new in the WHO 2022 classification of kidney tumours? |
title_fullStr | What’s new in the WHO 2022 classification of kidney tumours? |
title_full_unstemmed | What’s new in the WHO 2022 classification of kidney tumours? |
title_short | What’s new in the WHO 2022 classification of kidney tumours? |
title_sort | what’s new in the who 2022 classification of kidney tumours? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10342217/ https://www.ncbi.nlm.nih.gov/pubmed/36645398 http://dx.doi.org/10.32074/1591-951X-818 |
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