血液病理学
卡斯特曼病
淋巴增殖性病變
鉴别诊断
病理
淋巴瘤
医学
疾病
生物
细胞遗传学
染色体
生物化学
基因
作者
Gorana Gašljević,Arturo Bonometti,Ioannis Anagnostopoulos,Olga Balagué,Michiel van den Brand,James R. Cook,Camille Laurent,Maurilio Ponzoni,Leticia Quintanilla-Martı́nez,Birgitta Sander,S Dirnhofer
出处
期刊:Virchows Archiv
[Springer Nature]
日期:2025-07-12
卷期号:487 (2): 253-273
被引量:3
标识
DOI:10.1007/s00428-025-04171-w
摘要
Abstract Castleman disease (CD) is an intriguing and complicated group of local and systemic disorders mainly affecting lymph nodes with heterogeneous presentation and therapeutic needs. These disorders were the topic of Session 1 of the Lymphoma Workshop at the 2024 EA4HP in Dubrovnik, Croatia. In this report, we summarize the features of the 85 submitted cases and review the differential diagnosis, pitfalls, and advances for all CD subtypes. Specifically, the molecular landscape of unicentric CD and its relationship with follicular dendritic cell proliferations and indolent T-lymphoblastic proliferation will be discussed. The spectrum of idiopathic multicentric CD (MCD), TAFRO syndrome, as well as the clinical and histopathological peculiarities of POEMS-CD, is reviewed. Cases of Kaposi sarcoma-associated herpesvirus/human herpesvirus 8 (KSHV/HHV8) + MCD were the most complicated and well demonstrated the difficulties and overlaps in the differential diagnosis of KSHV/HHV8 + lymphoproliferative disorders. Finally, the important topic of CD mimickers will be addressed, demonstrating how the integration of clinical, laboratory, histopathological, and molecular data is mandatory to confirm a diagnosis of CD and how to distinguish it from the many neoplastic, autoimmune, and infective mimickers.
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