[髓样肿瘤合并大颗粒淋巴细胞增生的临床特征]。

Q3 Medicine
C X Du, G P Xiang, L Peng, X Y Xiao, G S Teng, Y H Zhang, Y Wang, Y F Duan, Z H Shao, J Bai
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引用次数: 0

摘要

髓样肿瘤(MNs)属于一类以造血干祖细胞生物功能异常为特征的血液恶性肿瘤。MN患者异常的免疫和造血微环境与恶性克隆造血干细胞相互作用,促进了其疾病的发生和发展。MN大颗粒淋巴细胞增生(MN-LGLP)是该类型疾病中一种特殊而罕见的临床现象。目前,国内外对该病的研究还很有限。本研究分析了该类型患者的临床和实验室特征,并探讨了LGLP对MN患者临床特征和生存期的影响。MN-LGLP患者容易出现中性粒细胞减少和脾肿大。LGLP的存在并不是影响MN-LGLP患者生存的风险因素。STAG、ASXL1和TET2是MN-LGLP最常见的伴随基因突变,MN-LGLP和STAG2突变的患者预后较差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical characteristics of myeloid tumors combined with the proliferation of large granular lymphocytes].

Myeloid neoplasms (MNs) belong to a group of hematological malignancies characterized by the abnormal biological functions of hematopoietic stem progenitor cells. The abnormal immune and hematopoietic microenvironment of patients with MN interact with malignant clonal hematopoietic stem cells, promoting the occurrence and development of their diseases. MN large granular lymphocyte proliferation (MN-LGLP) is a special and rare clinical phenomenon in this type of disease. Currently, research on this disease in domestic and international cohorts is limited. This study analyzes the clinical and laboratory characteristics of this type of patient and explores the impact of LGLP on the clinical characteristics and survival of patients with MN. Patients with MN-LGLP are prone to neutropenia and splenomegaly. The presence of LGLP is not a risk factor affecting the survival of patients with MN-LGLP. STAG, ASXL1, and TET2 are the most common accompanying gene mutations in MN-LGLP, and patients with MN-LGLP and STAG2 mutations have poor prognoses.

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