Finsen Laboratory, Biotech Research and Innovation Centre and Rigshospitalet, University of Copenhagen, Copenhagen, Denmark; and.
Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Blood. 2017 Jan 26;129(4):420-423. doi: 10.1182/blood-2016-10-743765. Epub 2016 Nov 30.
Hypodiploidy <40 chromosomes is an uncommon genetic feature of acute lymphoblastic leukemia (ALL) in both children and adults. It has long been clear by cytogenetic analyses, and recently confirmed by mutational profiling, that these cases may be further subdivided into 2 subtypes: near-haploid ALL with 24 to 30 chromosomes and low-hypodiploid ALL with 31 to 39 chromosomes. Both groups are associated with a very poor prognosis, and these patients are among those who could benefit most from novel treatments.
低倍体性<40 条染色体是儿童和成人急性淋巴细胞白血病(ALL)的一种罕见的遗传特征。通过细胞遗传学分析早已明确,最近通过突变分析也进一步证实,这些病例可进一步细分为 2 个亚型:近单体 ALL,染色体数为 24 至 30 条;低倍体性 ALL,染色体数为 31 至 39 条。这两组患者的预后均非常差,这些患者是最有可能从新型治疗中获益的人群之一。