髓样
肿瘤
髓系白血病
谱系(遗传)
生物
浆细胞样树突状细胞
癌症研究
骨髓增生性肿瘤
免疫学
病理
医学
基因
树突状细胞
抗原
骨髓
遗传学
骨髓纤维化
作者
Jianming Peng,Shaolong He,Xiaokui Yang,Liang Huang,Jia Wei
标识
DOI:10.1016/j.critrevonc.2023.104186
摘要
Plasmacytoid dendritic cells (pDCs) are a specific dendritic cell type stemming from the myeloid lineage. Clinically and pathologically, neoplasms associated with pDCs are classified as blastic plasmacytoid dendritic cell neoplasm (BPDCN), mature plasmacytoid dendritic myeloid neoplasm (MPDMN) and pDC expansion in myeloid neoplasms (MNs). BPDCN was considered a rare and aggressive neoplasm in the 2016 World Health Organization (WHO) classification. MPDMN, known as mature pDC-derived neoplasm, is closely related to MNs and was first recognized in the latest 2022 WHO classification, proposing a new concept that acute myeloid leukemia cases could show clonally expanded pDCs (pDC-AML). With the advances in detection techniques, an increasing number of pDC expansion in MNs have been reported, but whether the pathogenesis is similar to that of MPDMN remains unclear. This review focuses on patient characteristics, diagnosis and treatment of pDC expansion in MNs to gain further insight into this novel and unique provisional subtype.
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