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慢性髓性白血病样疾病的最新进展

Update on CML-Like Disorders.

机构信息

University of Southampton, Southampton, UK; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury, UK.

出版信息

Clin Lymphoma Myeloma Leuk. 2020 Sep;20 Suppl 1:S101-S102. doi: 10.1016/S2152-2650(20)30477-8.

Abstract

Chronic myeloid leukemia (CML) is defined for many years as BCR-ABL1 positive disease, but older publications refer to a poor prognosis, clinically heterogeneous entity termed 'BCR-ABL1 negative CML' constituting about 5% of CML cases. Apart from very rare CML cases with cytogenetically cryptic, atypical variant BCR-ABL1 fusions that had been inadvertently missed during the diagnostic work up, most of these cases would now be classified as a subtype of myelodysplastic/myeloproliferative neoplasm (MDS/MPN), such as atypical CML (aCML), chronic myelomonocytic leukemia (CMML), or chronic neutrophilic leukemia (CNL). A minority would be classified as systemic mastocytosis with associated hematological neoplasm (SM-AHN), myeloid/lymphoid neoplasms associated with eosinophilia and rearrangement of PDGFRA, PDGFRB, FGFR1 or with PCM1-JAK2 (MLN-eo), or chronic eosinophilic leukemia not otherwise specified (CEL-NOS)..

摘要

慢性髓性白血病(CML)多年来被定义为 BCR-ABL1 阳性疾病,但旧的出版物提到预后不良,临床上异质的实体称为“BCR-ABL1 阴性 CML”,约占 CML 病例的 5%。除了极少数在诊断工作中无意中遗漏的具有细胞遗传学隐匿性、非典型变异 BCR-ABL1 融合的罕见 CML 病例外,这些病例中的大多数现在将被归类为骨髓增生异常/骨髓增殖性肿瘤(MDS/MPN)的亚型,如不典型 CML(aCML)、慢性髓单核细胞白血病(CMML)或慢性中性粒细胞白血病(CNL)。少数将被归类为伴有血液系统肿瘤的系统性肥大细胞增多症(SM-AHN)、伴有嗜酸粒细胞增多和 PDGFRA、PDGFRB、FGFR1 重排的髓系/淋系肿瘤,或伴有 PCM1-JAK2(MLN-eo)的髓系/淋系肿瘤,或未特指的慢性嗜酸粒细胞白血病(CEL-NOS)。

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