Singh Aditi, Asghar Ishaq, Kohler Laura, Snower Daniel, Hakim Hosam, Lebovic Daniel
Department of Hematology and Oncology, Ascension St. John Hospital.
Department of Pathology, Ascension St. John Hospital.
Mediterr J Hematol Infect Dis. 2022 Mar 1;14(1):e2022018. doi: 10.4084/MJHID.2022.018. eCollection 2022.
In the modern era, classification of neoplasms not only depends on immunomorphological features but also on specific disease-defining genetic events. Translocations/rearrangements of MYC/8q24 locus combined with BCL-2 or BCL6 translocations (double/triple hit) are considered hallmarks of high-grade B-cell lymphoma (HGBL), a type of aggressive mature B-cell lymphoma. When cases with immature immunophenotypes present these rearrangements, diagnosis becomes very difficult. We herein report an unusual case of an aggressive B-cell lymphoma/leukemia that presented with immature morphology and immunophenotype with triple hit gene rearrangements. This case highlights the difficulty in classifying and appropriately treating these patients. The novel aspect is the treatment and outcome with chimeric antigen receptor or -cell .
在现代,肿瘤的分类不仅取决于免疫形态学特征,还取决于特定的疾病定义性基因事件。MYC/8q24位点的易位/重排与BCL-2或BCL6易位(双重/三重打击)相结合被认为是高级别B细胞淋巴瘤(HGBL)的标志,HGBL是一种侵袭性成熟B细胞淋巴瘤。当具有不成熟免疫表型的病例出现这些重排时,诊断变得非常困难。我们在此报告一例不寻常的侵袭性B细胞淋巴瘤/白血病病例,该病例呈现不成熟的形态学和免疫表型以及三重打击基因重排。该病例凸显了对这些患者进行分类和适当治疗的困难。新的方面是嵌合抗原受体或 -细胞的治疗及结果。