Indolent pediatric lymphomas/lymphoproliferative disorders: a report of the 2024 EA4HP/SH lymphoma workshop.

IF 3.4 3区 医学 Q1 PATHOLOGY
Leonie Frauenfeld, Maurilio Ponzoni, Gorana Gasljevic, Ioannis Anagnostopoulos, Michiel Van den Brand, James R Cook, Camille Laurent, Birgitta Sander, Stefan Dirnhofer, Leticia Quintanilla-Martinez, Olga Balague
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Abstract

The boundaries between indolent neoplastic and reactive lymphoproliferations were discussed during the 2024 European Association for Haematopathology/Society for Hematopathology workshop in Dubrovnik, Croatia. Session 4 focused on the revision of indolent pediatric lymphoid neoplasms/lymphoproliferations. Forty-one cases were submitted, representing good examples of indolent pediatric lymphomas/lymphoproliferations and their diagnostic challenges. The morphologic spectrum of pediatric-type follicular lymphoma (PTFL) was discussed, especially exploring unifying features of cases with and without marginal zone differentiation (MZD) (the first also referred to as pediatric nodal marginal zone lymphoma). Unusual features like relapses/recurrences; extranodal involvement and high proliferation rate in the marginal zone differentiated component were observed in PTFL with or without MZD. Rare follicle center-derived neoplasms occurring in children other than PTFL where discussed, such as primary testicular follicular lymphoma and follicle center lymphoma of the lower female genital tract. Testicular follicular lymphomas were compared to cases known from literature, defining a better picture of their clinicopathological features. The criteria for the diagnosis of atypical lymphoid hyperplasia were reviewed and nodal and extranodal cases are discussed. Plasmacytic proliferations in the pediatric population are exceedingly rare, but do exist in clonal and non-clonal forms. A heterogeneous group of extranodal lymphomas is included, among them extranodal marginal zone lymphomas (MZL) of the stomach with a large cell transformation and an intramuscular MZL with comparable features of a cutaneous MZL/lymphoproliferation with IgG4 expression. In this report, the different spectrum of indolent pediatric lymphomas compared to the adult counterpart will be highlighted, to avoid misdiagnosis and overtreatment.

惰性儿童淋巴瘤/淋巴增生性疾病:2024年EA4HP/SH淋巴瘤研讨会报告
在克罗地亚杜布罗夫尼克举行的2024年欧洲血液病理学协会/血液病理学学会研讨会上,讨论了惰性肿瘤和反应性淋巴细胞增生之间的界限。第4次会议的重点是小儿惰性淋巴样肿瘤/淋巴细胞增生的修订。41个病例被提交,代表了儿童惰性淋巴瘤/淋巴细胞增生的好例子及其诊断挑战。讨论了儿科型滤泡性淋巴瘤(PTFL)的形态学谱,特别是探讨了有无边缘区分化(MZD)病例的统一特征(前者也称为儿科淋巴结边缘区淋巴瘤)。不寻常的特征,如复发/复发;伴或不伴MZD的PTFL均可见结外受累和边缘区分化成分的高增殖率。除PTFL外发生于儿童的罕见滤泡中心源性肿瘤,如原发性睾丸滤泡淋巴瘤和下女性生殖道滤泡中心淋巴瘤。将睾丸滤泡性淋巴瘤与文献中已知的病例进行比较,以更好地了解其临床病理特征。本文回顾了非典型淋巴样增生的诊断标准,并讨论了淋巴结和结外病例。浆细胞增生在儿科人群是非常罕见的,但确实存在于克隆和非克隆形式。结外淋巴瘤包括异质性组,其中胃结外边缘区淋巴瘤(MZL)具有大细胞转化,肌内MZL具有与皮肤MZL/淋巴增生相似的特征,表达IgG4。在本报告中,小儿惰性淋巴瘤与成人惰性淋巴瘤的不同频谱将被突出显示,以避免误诊和过度治疗。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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