T and NK lymphoblastic leukemia/lymphoma: Report from the 2023 SH/EAHP Workshop.

IF 2.3 4区 医学 Q2 PATHOLOGY
Olga K Weinberg, Carlos E Bueso-Ramos, Rashmi Kanagal-Shamanna
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引用次数: 0

Abstract

Objectives: The 2023 Society for Hematopathology/European Association for Hematopathology Workshop addressed advancements in the diagnosis and classification of T- and natural killer (NK)-cell lymphomas/leukemias.

Methods: Session 8 of the workshop collected a diverse set of 38 cases of immature T- and NK-cell lymphoma/leukemias, as well as acute leukemia of ambiguous lineage (ALAL) and other miscellaneous cases, including indolent T-lymphoblastic proliferations.

Results: Twenty patients with T-lymphoblastic leukemia/lymphoma (T-LBL/L) and 3 patients with early T-cell precursor acute lymphoblastic leukemia (ETP-ALL) presented at a median age of 21.5 years. Male sex was predominant (70% of all cases), with 40% having a mediastinal mass. Cases (60%) were negative for both CD34 and TdT. In addition, 7 ALAL and 3 mixed phenotype acute leukemia, T/myeloid subtypes were submitted with a median presenting age of 16 (range, 11-56) years, and most patients (67%) frequently showed adenopathy or splenomegaly. A single case of NK acute lymphoblastic leukemia was also submitted.

Conclusions: This session highlighted unusual T-LBL/L cases with expression of cytotoxic markers, γ/δ phenotype, a more mature immunophenotype, and ALAL that are challenging to classify. Among T-ALL cases, interesting relapse changes were identified, with 1 patient developing a mature NK-cell phenotype. Patients with ALAL presented in an unusual setting of prior therapy or a germline mutation.

T和NK淋巴细胞白血病/淋巴瘤:2023年SH/EAHP研讨会报告。
2023年欧洲血液病理学协会/血液病理学协会研讨会讨论了T细胞和自然杀伤细胞淋巴瘤/白血病的诊断和分类进展。方法:研讨会第8次会议收集了38例不同类型的未成熟T细胞和nk细胞淋巴瘤/白血病,以及不明谱系的急性白血病(ALAL)和其他杂项病例,包括惰性T淋巴细胞增殖。结果:20例t淋巴母细胞白血病/淋巴瘤(T-LBL/L)患者和3例早期t细胞前体急性淋巴母细胞白血病(ETP-ALL)患者,中位年龄21.5岁。男性居多(占所有病例的70%),其中40%有纵隔肿块。60%的病例CD34和TdT均为阴性。此外,7例ALAL和3例混合表型急性白血病,T/髓系亚型,中位表现年龄为16岁(范围11-56岁),大多数患者(67%)经常表现为腺病或脾肿大。报告了一例NK急性淋巴细胞白血病。结论:本次会议强调了具有细胞毒性标志物、γ/δ表型、更成熟的免疫表型和ALAL表达的异常T-LBL/L病例,这些病例具有挑战性的分类。在T-ALL病例中,发现了有趣的复发变化,1例患者发展为成熟的nk细胞表型。ALAL患者表现为不寻常的既往治疗或种系突变。
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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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