Deshmukh Komal Galani, Kelemen Katalin
Star Superspeciality Hospital, Nagpur 440012, India.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Phoenix, AZ 85054, USA.
Life (Basel). 2022 Apr 8;12(4):559. doi: 10.3390/life12040559.
Donor-cell derived myeloid neoplasm (DDMN), a rare complication after allogeneic hematopoietic cell transplantation (HCT), is of interest for its potential to reveal donor-derived and host-derived factors that contribute to the pathogenesis of leukemia. The accurate diagnosis of donor-derived leukemias has been facilitated by the more frequent use of molecular techniques. In this study, we describe three additional cases of DDMN; the first reported case of donor-derived chronic myelomonocytic leukemia (CMML), one acute myeloid leukemia (AML) with t(8;21)(q22;22); and one donor-derived MDS with deletion 5q. A review of the cytogenetic profiles of previously reported DDMN indicates a significant contribution of therapy-related myeloid neoplasms. Cases with direct evidence of donor- or recipient-dependent factors are rare; a role of direct transfer of leukemic cells, genomic instability of the donor, abnormal gene methylation in donor cells, proleukemic potential of abnormal stromal niche, and the role of immunological surveillance after transplantation has been observed. The role of additional potential pathogenetic factors that are without clinically observed evidence are also reviewed.
供体细胞衍生的髓系肿瘤(DDMN)是异基因造血细胞移植(HCT)后一种罕见的并发症,因其有可能揭示导致白血病发病机制的供体来源和宿主来源因素而备受关注。分子技术的更频繁使用有助于准确诊断供体来源的白血病。在本研究中,我们描述了另外三例DDMN;首例报告的供体来源的慢性粒单核细胞白血病(CMML)、一例伴有t(8;21)(q22;22)的急性髓系白血病(AML)以及一例伴有5q缺失的供体来源的骨髓增生异常综合征(MDS)。对先前报道的DDMN的细胞遗传学特征进行回顾表明,治疗相关髓系肿瘤起了重要作用。有供体或受体依赖性因素直接证据的病例很少见;已观察到白血病细胞的直接转移、供体的基因组不稳定性、供体细胞中异常的基因甲基化、异常基质微环境的白血病前期潜能以及移植后免疫监视的作用。还对没有临床观察证据的其他潜在致病因素的作用进行了综述。