Egan Caoimhe, Song Sophie, Liu Wei-Ping, Wang Zhe, Xiao Wenbin, Chan John K C, Dirnhofer Stefan, Fend Falko, Goodlad John R, Li Xiaoqiu, Lorsbach Robert, Emile Jean-Francois
Haematopathology and Oncology Diagnostic Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Department of Pathology and Laboratory Medicine, UCLA Health/David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Virchows Arch. 2025 Jun 24. doi: 10.1007/s00428-025-04114-5.
Histiocytic and dendritic cell neoplasms of hematopoietic origin are derived from or show differentiation towards the cells of the mononuclear phagocyte system. Plasmacytoid dendritic cell proliferations/neoplasms include mature plasmacytoid dendritic cell proliferations identified in the context of a defined myeloid neoplasm and blastic plasmacytoid dendritic cell neoplasm, an aggressive tumor with a poor outcome. Malignant histiocytic (macrophage/dendritic cell) neoplasms occur de novo or in the setting of another hematological malignancy, typically "transdifferentiated" from associated lymphoid neoplasia. Recurrent alterations in the MAPK pathway have been shown to have a key role in their pathogenesis. Neoplasms derived from follicular dendritic cells and fibroblastic reticular cells originate from a mesenchymal precursor. The major entities in this group include follicular dendritic sarcoma, which has recently been shown to harbor recurrent alterations in NF-κB pathway genes, and EBV positive inflammatory follicular dendritic cell sarcoma/tumor, a rare lesion with an inflammatory pseudotumor-like morphology and association with EBV infection. At the joint Workshop of the Chinese Society of Hematopathology (CSHP), the European Association for Haematopathology (EA4HP) and the Society for Hematopathology (SH) on histiocytic/dendritic cell proliferations, neoplasms, and their mimics in Hefei, China, April 2024, there were 16 cases submitted to session 3 on plasmacytoid dendritic cell proliferations and neoplasms, and a total of 42 submissions to session 4 on malignant histiocytic and dendritic cell neoplasms, including stroma-derived neoplasms. A summary of the findings and conclusions arising from discussion of the workshop cases are presented in this report.
造血起源的组织细胞和树突状细胞肿瘤源自单核吞噬细胞系统的细胞或显示向其分化。浆细胞样树突状细胞增殖/肿瘤包括在特定髓系肿瘤背景下识别出的成熟浆细胞样树突状细胞增殖以及浆细胞样树突状细胞母细胞瘤,这是一种预后不良的侵袭性肿瘤。恶性组织细胞(巨噬细胞/树突状细胞)肿瘤可原发发生或在另一种血液系统恶性肿瘤的背景下出现,通常从相关淋巴样肿瘤“转分化”而来。已表明丝裂原活化蛋白激酶(MAPK)途径的反复改变在其发病机制中起关键作用。源自滤泡树突状细胞和成纤维网状细胞的肿瘤起源于间充质前体。该组中的主要实体包括滤泡树突状细胞肉瘤,最近已显示其在核因子κB(NF-κB)途径基因中存在反复改变,以及EB病毒阳性炎症性滤泡树突状细胞肉瘤/肿瘤,这是一种罕见病变,具有炎症性假瘤样形态且与EB病毒感染有关。在中国合肥举行的2024年4月中华血液病理学学会(CSHP)、欧洲血液病理学协会(EA4HP)和血液病理学学会(SH)关于组织细胞/树突状细胞增殖、肿瘤及其模仿病变的联合研讨会上,有16例病例提交至关于浆细胞样树突状细胞增殖和肿瘤的第3场会议,共有42份病例提交至关于恶性组织细胞和树突状细胞肿瘤(包括基质来源肿瘤)的第4场会议。本报告介绍了对研讨会上病例讨论得出的结果和结论的总结。