ZNF384重排急性白血病系列的临床病理和免疫表型特征

IF 0.9 4区 医学
Tharageswari Srinivasan, Praveen Sharma, Man Updesh Singh Sachdeva, Srinivasan Peyam, Lekshmon KS, Alka Khadwal, Sreejesh Sreedharanunni
{"title":"ZNF384重排急性白血病系列的临床病理和免疫表型特征","authors":"Tharageswari Srinivasan, Praveen Sharma, Man Updesh Singh Sachdeva, Srinivasan Peyam, Lekshmon KS, Alka Khadwal, Sreejesh Sreedharanunni","doi":"10.1007/s12288-024-01755-5","DOIUrl":null,"url":null,"abstract":"<p>Rearrangement involving <i>ZNF384</i> gene (<i>ZNF384</i>-r) is recently being described in acute leukemias. We present the clinic-pathological and immunophenotypic findings in a series of five cases of acute leukemia with <i>ZNF384</i>-r reported in our Institute between September 2020 to September 2023. Notably, while <i>TCF3::ZNF384</i> fusion was the most frequently encountered abnormality, the fusion partner was not identified in two patients with <i>ZNF384</i>-r BCP-ALL. Immunophenotypically, patients presenting as B-cell precursor acute lymphoblastic leukemia (BCP-ALL) had a distinct profile characterized by weak or absent CD10 expression and the presence of myeloid markers such as CD13/CD33. Our findings underscore the importance of recognizing the distinct immunophenotypic features of ZNF384-r leukemias, particularly in cases presenting with atypical BCP-ALL or B/Myeloid mixed phenotype acute leukemia phenotypes. Moreover, these findings highlight the necessity for tailored diagnostic algorithms in clinical laboratories to facilitate the timely and accurate diagnosis of this clinically relevant leukemia subtype.</p>","PeriodicalId":13314,"journal":{"name":"Indian Journal of Hematology and Blood Transfusion","volume":"50 1","pages":""},"PeriodicalIF":0.9000,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinicopathological and Immunophenotypic Characteristics of Series of ZNF384 Re-arranged Acute Leukemias\",\"authors\":\"Tharageswari Srinivasan, Praveen Sharma, Man Updesh Singh Sachdeva, Srinivasan Peyam, Lekshmon KS, Alka Khadwal, Sreejesh Sreedharanunni\",\"doi\":\"10.1007/s12288-024-01755-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Rearrangement involving <i>ZNF384</i> gene (<i>ZNF384</i>-r) is recently being described in acute leukemias. We present the clinic-pathological and immunophenotypic findings in a series of five cases of acute leukemia with <i>ZNF384</i>-r reported in our Institute between September 2020 to September 2023. Notably, while <i>TCF3::ZNF384</i> fusion was the most frequently encountered abnormality, the fusion partner was not identified in two patients with <i>ZNF384</i>-r BCP-ALL. Immunophenotypically, patients presenting as B-cell precursor acute lymphoblastic leukemia (BCP-ALL) had a distinct profile characterized by weak or absent CD10 expression and the presence of myeloid markers such as CD13/CD33. Our findings underscore the importance of recognizing the distinct immunophenotypic features of ZNF384-r leukemias, particularly in cases presenting with atypical BCP-ALL or B/Myeloid mixed phenotype acute leukemia phenotypes. Moreover, these findings highlight the necessity for tailored diagnostic algorithms in clinical laboratories to facilitate the timely and accurate diagnosis of this clinically relevant leukemia subtype.</p>\",\"PeriodicalId\":13314,\"journal\":{\"name\":\"Indian Journal of Hematology and Blood Transfusion\",\"volume\":\"50 1\",\"pages\":\"\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2024-04-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Hematology and Blood Transfusion\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s12288-024-01755-5\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Hematology and Blood Transfusion","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12288-024-01755-5","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

最近在急性白血病中发现了ZNF384基因重排(ZNF384-r)。我们介绍了本研究所在2020年9月至2023年9月期间报告的5例ZNF384-r急性白血病患者的临床病理和免疫表型结果。值得注意的是,虽然TCF3::ZNF384融合是最常见的异常,但在两例ZNF384-r BCP-ALL患者中并未发现融合伙伴。从免疫表型上看,表现为B细胞前体急性淋巴细胞白血病(BCP-ALL)的患者具有独特的特征,即CD10表达较弱或缺失,而CD13/CD33等髓系标志物存在。我们的发现强调了识别 ZNF384-r 白血病独特免疫表型特征的重要性,尤其是在出现非典型 BCP-ALL 或 B 型/髓系混合表型急性白血病表型的病例中。此外,这些研究结果还突显了临床实验室定制诊断算法的必要性,以便及时准确地诊断这种与临床相关的白血病亚型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinicopathological and Immunophenotypic Characteristics of Series of ZNF384 Re-arranged Acute Leukemias

Clinicopathological and Immunophenotypic Characteristics of Series of ZNF384 Re-arranged Acute Leukemias

Rearrangement involving ZNF384 gene (ZNF384-r) is recently being described in acute leukemias. We present the clinic-pathological and immunophenotypic findings in a series of five cases of acute leukemia with ZNF384-r reported in our Institute between September 2020 to September 2023. Notably, while TCF3::ZNF384 fusion was the most frequently encountered abnormality, the fusion partner was not identified in two patients with ZNF384-r BCP-ALL. Immunophenotypically, patients presenting as B-cell precursor acute lymphoblastic leukemia (BCP-ALL) had a distinct profile characterized by weak or absent CD10 expression and the presence of myeloid markers such as CD13/CD33. Our findings underscore the importance of recognizing the distinct immunophenotypic features of ZNF384-r leukemias, particularly in cases presenting with atypical BCP-ALL or B/Myeloid mixed phenotype acute leukemia phenotypes. Moreover, these findings highlight the necessity for tailored diagnostic algorithms in clinical laboratories to facilitate the timely and accurate diagnosis of this clinically relevant leukemia subtype.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
82
期刊介绍: Indian Journal of Hematology and Blood Transfusion is a medium for propagating and exchanging ideas within the medical community. It publishes peer-reviewed articles on a variety of aspects of clinical hematology, laboratory hematology and hemato-oncology. The journal exists to encourage scientific investigation in the study of blood in health and in disease; to promote and foster the exchange and diffusion of knowledge relating to blood and blood-forming tissues; and to provide a forum for discussion of hematological subjects on a national scale. The Journal is the official publication of The Indian Society of Hematology & Blood Transfusion.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信