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特发性和克隆性血细胞减少症的不明意义(ICUS 或 CCUS)是什么时候?

When are idiopathic and clonal cytopenias of unknown significance (ICUS or CCUS)?

机构信息

Division of Hematology and Hematologic Malignancies, University of Utah, Salt Lake City, UT.

出版信息

Hematology Am Soc Hematol Educ Program. 2021 Dec 10;2021(1):399-404. doi: 10.1182/hematology.2021000272.

Abstract

Rapid advances in sequencing technology have led to the identification of somatic mutations that predispose a significant subset of the aging population to myeloid malignancies. Recently recognized myeloid precursor conditions include clonal hematopoiesis of indeterminate potential (CHIP) and clonal cytopenia of unknown significance (CCUS). These conditions can present diagnostic challenges and produce unwarranted anxiety in some instances. While the risk of progression to myeloid malignancies is very low in CHIP, true CCUS confers an exponential increase in risk. Idiopathic cytopenia of unknown significance (IDUS) lacks the predisposing genetic mutations and has a variable course. In this review we define the early myeloid precursor conditions and their risk of progression. We present our diagnostic approach to patients with unexplained cytopenias and discuss the clinical consequences of CHIP and CCUS.

摘要

测序技术的快速发展已经确定了导致相当一部分老年人群易患髓系恶性肿瘤的体细胞突变。最近被认识到的髓系前体疾病包括不确定潜能的克隆性造血(CHIP)和意义未明的克隆性血细胞减少症(CCUS)。这些疾病在某些情况下可能会带来诊断上的挑战,并产生不必要的焦虑。虽然 CHIP 进展为髓系恶性肿瘤的风险非常低,但真正的 CCUS 会使风险呈指数级增加。特发性血细胞减少症不明原因(IDUS)缺乏致病的基因突变,病程具有多变性。在这篇综述中,我们定义了早期髓系前体疾病及其进展风险。我们提出了我们对不明原因血细胞减少症患者的诊断方法,并讨论了 CHIP 和 CCUS 的临床后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0da3/8791167/e23268431517/hem.2021000272_s1.jpg

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