The expanding spectrum of T-cell lymphomas with follicular helper T-cell phenotype and implications for differential diagnoses: A report of the 2023 SH/EA4HP Lymphoma Workshop.

IF 1.9 4区 医学 Q2 PATHOLOGY
Ahmet Dogan, Ozgur Can Eren, Laurence de Leval
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引用次数: 0

Abstract

Objectives: The 2023 Society of Hematopathology/European Association for Haematopathology Workshop on Progress in Peripheral T- and NK-Cell Lymphomas addressed challenges in diagnosis, biomarkers, and molecular pathogenesis.

Methods: Session 1 of the workshop focused on T-follicular helper (TFH) lymphomas and related entities. Sixty-one cases were submitted, and their histology, phenotype, and genetics were reviewed.

Results: The panelists confirmed 46 cases as TFH lymphomas, more commonly angioimmunoblastic type than follicular or not otherwise specified. A small subset of patients were young adults. Expected immunophenotypic profile, with expression of pan T-cell markers and TFH-specific markers with subtle differences between the histologic subtypes was observed. Genetic analyses revealed classic genetic alterations associated with these tumors, including frequent mutations in epigenetic modifiers (eg, TET2, DNMT3A, and IDH2) and RHOA. A broad spectrum of clonal B-cell proliferations was associated with TFH lymphomas, including polymorphic proliferations to large B-cell lymphoma-like expansions, often associated with Epstein-Barr virus. The remaining 15 cases were reclassified with alternative diagnoses, underscoring the diagnostic challenges and complexity in distinguishing TFH lymphomas from other entities.

Conclusions: The cases highlighted the clinical and biological heterogeneity and complexity of TFH lymphomas and provided a framework for pathology workup and diagnosis as well as future research.

具有滤泡辅助性t细胞表型的t细胞淋巴瘤的扩大谱及其对鉴别诊断的意义:2023年SH/EA4HP淋巴瘤研讨会的一份报告
2023年血液病理学学会/欧洲血液病理学协会关于外周血T细胞和nk细胞淋巴瘤进展的研讨会讨论了诊断、生物标志物和分子发病机制方面的挑战。方法:研讨会的第一部分集中在t -滤泡辅助淋巴瘤(TFH)和相关实体。本文对61例患者的组织学、表型和遗传学进行了回顾性分析。结果:小组成员确认46例为TFH淋巴瘤,更常见的是血管免疫母细胞型而不是滤泡型或无其他特殊说明。一小部分患者是年轻人。观察到预期的免疫表型谱,泛t细胞标记物和tfh特异性标记物的表达在组织学亚型之间存在细微差异。遗传分析揭示了与这些肿瘤相关的经典遗传改变,包括表观遗传修饰因子(如TET2、DNMT3A和IDH2)和RHOA的频繁突变。广谱克隆b细胞增殖与TFH淋巴瘤相关,包括多形性增殖到大b细胞淋巴瘤样扩张,通常与eb病毒相关。其余15例患者被重新分类为其他诊断,强调了将TFH淋巴瘤与其他实体区分的诊断挑战和复杂性。结论:这些病例突出了TFH淋巴瘤的临床和生物学异质性和复杂性,为病理检查和诊断以及未来的研究提供了框架。
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来源期刊
CiteScore
7.70
自引率
2.90%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The American Journal of Clinical Pathology (AJCP) is the official journal of the American Society for Clinical Pathology and the Academy of Clinical Laboratory Physicians and Scientists. It is a leading international journal for publication of articles concerning novel anatomic pathology and laboratory medicine observations on human disease. AJCP emphasizes articles that focus on the application of evolving technologies for the diagnosis and characterization of diseases and conditions, as well as those that have a direct link toward improving patient care.
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