Skhoun Hanaa, Khattab Mohammed, Chebihi Zahra Takki, Belkhayat Aziza, Dakka Nadia, BaghdadI Jamila El
Genetics Unit, Military Hospital Mohammed V, Rabat, Morocco.
Laboratory of Human Pathologies Biology, Department of Biology, Faculty of Sciences, and Genomic Center of Human Pathologies, Faculty of Medicine and Pharmacy, Mohammed V University in Rabat, Rabar, Morocco.
Leuk Res Rep. 2022 Jan 15;17:100289. doi: 10.1016/j.lrr.2022.100289. eCollection 2022.
Acute leukemias are often of myeloid or lymphoid origin. However, some acute leukemias revealed an undefined differentiation into a single lineage. Mixed phenotype acute leukemia (MPAL) is an uncommon diagnosis were blasts can share B/T/myeloid phenotype. Here, we report a rare case of a 17-year-old Moroccan female diagnosed with B/T mixed phenotype acute leukemia and a high hyperdiploid karyotype who relapsed after one year of complete remission with a lineage switch to B-cell acute lymphoblastic leukemia. This case report corroborates the disclosed findings about the high occurence of abnormal karyotypes and poor prognosis of MPAL.
急性白血病通常起源于髓系或淋巴系。然而,一些急性白血病显示出向单一谱系的未明确分化。混合表型急性白血病(MPAL)是一种罕见的诊断,其原始细胞可具有B/T/髓系表型。在此,我们报告一例罕见病例,一名17岁摩洛哥女性被诊断为B/T混合表型急性白血病且具有高超二倍体核型,在完全缓解一年后复发,谱系转变为B细胞急性淋巴细胞白血病。本病例报告证实了已公开的关于MPAL异常核型高发生率和预后不良的研究结果。