Mesh : Humans Leukemia, Myeloid, Acute / diagnosis genetics Signal Transduction Mutation Clone Cells Prognosis Receptors, Colony-Stimulating Factor / genetics Leukemia Hypereosinophilic Syndrome

来  源:   DOI:10.7754/Clin.Lab.2023.230924

Abstract:
BACKGROUND: Chronic eosinophilic leukemia (CEL) is a rare invasive disease characterized by non-specific cytogenetic abnormalities or elevated mother cells, poor prognosis, and a high risk of conversion to acute leukemia.
METHODS: We described the data of a patient with CEL-NOS.
RESULTS: This case is a CEL-NOS with four mutations in CSF3R-T618I, DNMT3A Q816, ASXL1, and IDH2.
CONCLUSIONS: The patient rapidly evolves into secondary acute myeloid leukemia (AML).
摘要:
背景:慢性嗜酸性粒细胞白血病(CEL)是一种罕见的侵袭性疾病,其特征是非特异性细胞遗传学异常或母细胞升高,预后不良,和转化为急性白血病的高风险。
方法:我们描述了CEL-NOS患者的数据。
结果:本病例为CEL-NOS,CSF3R-T618I有4个突变,DNMT3AQ816、ASXL1和IDH2。
结论:患者迅速发展为继发性急性髓性白血病(AML)。
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