Epstein-Barr virus-positive T- and NK-cell lymphoproliferative disorders: Report from the 2023 SH/EA4HP Lymphoma Workshop.

IF 2.3 4区 医学 Q2 PATHOLOGY
Leticia Quintanilla-Martinez, Shaoying Li, Amy Chadburn
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引用次数: 0

Abstract

Objectives: To summarize the conclusions of the 2023 Society for Hematopathology/European Association for Haematopathology workshop regarding Epstein-Barr virus (EBV)-positive T- and natural killer (NK)-cell lymphoproliferative disorders (LPDs).

Methods: There were 38 cases submitted to session 3 of the workshop.

Results: Cases included extranodal NK/T-cell lymphoma (ENKTCL), nasal type (n = 16), EBV+ T- and NK-cell LPDs in children (n = 12), primary nodal EBV+ T- and NK-cell lymphoma (n = 5), and other EBV+ T- and NK-cell LPDs (n = 5). The ENKTCL cases highlighted some unusual features like indolent behavior, small cell morphology, and T-cell phenotype, including cases with CD4 and CD30 expression. The differential diagnosis of ENKTCL was illustrated by 4 cases with other primary cutaneous lymphomas. The difficulty in the diagnosis of systemic chronic active EBV disease, its complications, and the sometimes elusive boundaries among the EBV+ LPDs in children are also discussed. The submitted cases also unveiled cases of EBV+ γδ T-cell leukemia/lymphoma not recognized under current classifications and cases of EBV+ CD8+ cytotoxic lymphomas associated with treatment for B-cell lymphomas. The need to have a low threshold to investigate the presence of EBV is highlighted.

Conclusions: The diagnosis of EBV+ T- and NK-cell LPDs is complex and requires a multiparameter approach incorporating clinical information and morphologic and molecular features.

eb病毒阳性T细胞和nk细胞淋巴增生性疾病:来自2023年SH/EA4HP淋巴瘤研讨会的报告
目的:总结2023年血液病理学学会/欧洲血液病理学协会研讨会关于eb病毒(EBV)阳性T-和自然杀伤(NK)细胞淋巴增生性疾病(lpd)的结论。方法:将38例病例提交研讨会第三期。结果:结外NK/T细胞淋巴瘤(ENKTCL),鼻型(n = 16), EBV+ T细胞和NK细胞lpd (n = 12),原发性淋巴结EBV+ T细胞和NK细胞淋巴瘤(n = 5),其他EBV+ T细胞和NK细胞lpd (n = 5)。ENKTCL病例突出了一些不寻常的特征,如惰性行为、小细胞形态和t细胞表型,包括CD4和CD30表达的病例。以4例其他原发性皮肤淋巴瘤为例,分析了ENKTCL的鉴别诊断。我们还讨论了诊断全身性慢性活动性EBV疾病的困难、其并发症以及儿童EBV+ lpd之间有时难以捉摸的界限。提交的病例还揭示了目前分类中未识别的EBV+ γδ t细胞白血病/淋巴瘤病例,以及与b细胞淋巴瘤治疗相关的EBV+ CD8+细胞毒性淋巴瘤病例。需要有一个较低的阈值来调查EBV的存在是突出的。结论:EBV+ T细胞和nk细胞lpd的诊断是复杂的,需要结合临床信息、形态学和分子特征的多参数方法。
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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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