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中性粒细胞骨髓肿瘤的诊断与治疗。

Diagnosis and management of neutrophilic myeloid neoplasms.

机构信息

Division of Hematology, Stanford University School of Medicine/Stanford Cancer Institute, Stanford, California.

出版信息

Clin Adv Hematol Oncol. 2021 Jul;19(7):450-459.

Abstract

Chronic neutrophilia is commonly seen with persistent infections, inflammatory disorders, smoking, solid tumors, and specific medications. However, after reactive causes have been excluded, a workup for primary (clonal) neutrophilic disorders, such as myeloproliferative neoplasms (MPNs) and myelodysplastic/myeloproliferative overlap syndromes, should be pursued. Except for chronic myeloid leukemia, which is defined by the presence of the Philadelphia (Ph) chromosome, and the classic Ph chromosome-negative MPNs (polycythemia vera, essential thrombocythemia, and primary myelofibrosis), clonal neutrophilic neoplasms historically have been challenging to diagnose and classify. The 2016 revised World Health Organization classification of these disorders has been based mainly on clinicopathologic features. However, recent discoveries of the molecular alterations underlying these disorders have served to supplement our knowledge of their morphologic and clinical features, opening new therapeutic avenues. In this review, we discuss the diagnostic approach, prognostic features, and treatments of neutrophilic myeloid neoplasms, with a focus on chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia.

摘要

慢性中性粒细胞增多症常见于持续性感染、炎症性疾病、吸烟、实体瘤和特定药物。然而,在排除反应性原因后,应进行原发性(克隆性)中性粒细胞疾病的检查,如骨髓增殖性肿瘤(MPN)和骨髓增生异常/骨髓增殖性重叠综合征。除了由费城(Ph)染色体定义的慢性髓性白血病,以及经典的 Ph 染色体阴性 MPN(真性红细胞增多症、特发性血小板增多症和原发性骨髓纤维化)外,克隆性中性粒细胞肿瘤的诊断和分类一直具有挑战性。2016 年修订的世界卫生组织(WHO)对这些疾病的分类主要基于临床病理特征。然而,最近发现这些疾病的分子改变有助于补充我们对其形态和临床特征的认识,为新的治疗方法开辟了道路。在这篇综述中,我们讨论了中性粒细胞髓系肿瘤的诊断方法、预后特征和治疗方法,重点介绍慢性中性粒细胞白血病、不典型慢性髓性白血病和慢性髓单核细胞白血病。

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