Genetic studies in clonal haematopoiesis, myelodysplastic neoplasms and acute myeloid leukaemia – a practical guide to WHO-HAEM5

IF 1.1 4区 生物学 Medizinische Genetik Pub Date : 2024-03-04 DOI:10.1515/medgen-2024-2010
Katharina Hörst, Constanze Kühn, C. Haferlach, T. Haferlach, Joseph D. Khoury
{"title":"Genetic studies in clonal haematopoiesis, myelodysplastic neoplasms and acute myeloid leukaemia – a practical guide to WHO-HAEM5","authors":"Katharina Hörst, Constanze Kühn, C. Haferlach, T. Haferlach, Joseph D. Khoury","doi":"10.1515/medgen-2024-2010","DOIUrl":null,"url":null,"abstract":"\n In recent years, technology developments and increase in knowledge have led to profound changes in the diagnostics of haematologic neoplasms, particularly myeloid neoplasms. Therefore an updated, fifth edition of the World Health Organization (WHO) classification of haematolymphoid neoplasms (WHO-HAEM5) will be issued in 2024. In this context, we present a practical guide for analysing the genetic aspects of clonal haematopoiesis of indeterminate potential (CHIP), clonal cytopenia of undetermined significance (CCUS), myelodysplastic neoplasms (MDS), and acute myeloid leukaemia (AML) based on WHO-HAEM5. This guide navigates through the genetic abnormalities underlying myeloid neoplasms which are required to be detected for classification according to WHO-HAEM5 and provides diagnostic algorithms.","PeriodicalId":51130,"journal":{"name":"Medizinische Genetik","volume":"103 23","pages":""},"PeriodicalIF":1.1000,"publicationDate":"2024-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medizinische Genetik","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1515/medgen-2024-2010","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In recent years, technology developments and increase in knowledge have led to profound changes in the diagnostics of haematologic neoplasms, particularly myeloid neoplasms. Therefore an updated, fifth edition of the World Health Organization (WHO) classification of haematolymphoid neoplasms (WHO-HAEM5) will be issued in 2024. In this context, we present a practical guide for analysing the genetic aspects of clonal haematopoiesis of indeterminate potential (CHIP), clonal cytopenia of undetermined significance (CCUS), myelodysplastic neoplasms (MDS), and acute myeloid leukaemia (AML) based on WHO-HAEM5. This guide navigates through the genetic abnormalities underlying myeloid neoplasms which are required to be detected for classification according to WHO-HAEM5 and provides diagnostic algorithms.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
克隆性造血、骨髓增生异常肿瘤和急性髓性白血病的基因研究--WHO-HAEM5 实用指南
近年来,技术的发展和知识的增长使血液肿瘤,尤其是骨髓肿瘤的诊断发生了深刻的变化。因此,世界卫生组织(WHO)第五版血液淋巴肿瘤分类(WHO-HAEM5)将于 2024 年发布。在此背景下,我们根据 WHO-HAEM5 提出了一份实用指南,用于分析具有不确定潜能的克隆性造血(CHIP)、意义未定的克隆性细胞减少症(CCUS)、骨髓增生异常性肿瘤(MDS)和急性髓性白血病(AML)的遗传学问题。本指南介绍了根据 WHO-HAEM5 进行分类时需要检测的髓系肿瘤基础基因异常,并提供了诊断算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Medizinische Genetik
Medizinische Genetik GENETICS & HEREDITY-
自引率
9.10%
发文量
48
期刊介绍: medizinischegenetik is a scientific journal that is owned and published by the German Society of Human Genetics e.V. since 1989. The journal was founded by Prof. Jan Murken, München. Self-published until 2006, from 2007-2019 published at Springer Verlag and since 2020 at De Gruyter. medizinischegenetik serves education and training among colleagues, the interdisciplinary exchange of knowledge in all areas of human genetics in clinics, practice, research and teaching. Each issue of the quarterly journal deals with a focus that provides a comprehensive overview of current developments in specific clinical pictures, technical developments and therapeutic approaches. All reviews are written in English language. The journal thus creates a platform for the international exchange of knowledge and increased awareness of German research activities in the scientific community. In addition, medizinischegenetik contains information on activities in its own subject in the German-language section. This includes conference reports, association announcements, personnel matters, statements and guidelines. With health policy questions, historical retrospectives and comments on current developments, the profession takes a stand on human genetic issues in Germany, Austria and Switzerland.
期刊最新文献
"Wir gründeten die Zeitschrift medizinischegenetik, weil die Humangenetiker ein Forum für ihr Fach brauchten": Der Initiator Prof. Dr. med. Jan Murken über die Herausforderungen und Notwendigkeiten, in den ausgehenden 80er Jahren eine deutschsprachige Zeitschrift zu gründen - ein Interview anlässlich seines 90. Geburtstags. 10 Years of International Albinism Awareness: United Nations celebrate an anniversary and a decade of collective progress, but challenges remain. 37. Tumorgenetische Arbeitstagung: 8.–10. Mai 2025, Leipzig. Genetics of female and male infertility. GfH-Promotionspreise 2024.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1