Srinivasan Tharageswari, Sharma Praveen, Sachdeva Man Updesh Singh, Peyam Srinivasan, Ks Lekshmon, Khadwal Alka, Sreedharanunni Sreejesh
Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012 India.
Department of Pediatrics (Pediatric Hematology and Oncology Division), Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Indian J Hematol Blood Transfus. 2024 Oct;40(4):704-709. doi: 10.1007/s12288-024-01755-5. Epub 2024 Apr 9.
Rearrangement involving gene (-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 -r reported in our Institute between September 2020 to September 2023. Notably, while fusion was the most frequently encountered abnormality, the fusion partner was not identified in two patients with -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.
涉及基因(-r)的重排在急性白血病中最近有所报道。我们展示了2020年9月至2023年9月期间在我们研究所报告的一系列5例伴有-r的急性白血病的临床病理和免疫表型结果。值得注意的是,虽然融合是最常遇到的异常情况,但在两名伴有-r的B细胞前体急性淋巴细胞白血病(BCP-ALL)患者中未鉴定出融合伙伴。免疫表型方面,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,其特点是CD10表达弱或缺失,以及存在髓系标志物如CD13/CD33。我们的研究结果强调了认识ZNF384-r白血病独特免疫表型特征的重要性,特别是在表现为非典型BCP-ALL或B/髓系混合表型急性白血病表型的病例中。此外,这些发现突出了临床实验室中定制诊断算法的必要性,以促进对这种临床相关白血病亚型的及时准确诊断。