滤泡性辅助性t细胞淋巴瘤伴霍奇金/ reed - sternberg样细胞与经典霍奇金淋巴瘤的比较研究

IF 4.5 1区 医学 Q1 PATHOLOGY American Journal of Surgical Pathology Pub Date : 2025-03-01 Epub Date: 2025-01-06 DOI:10.1097/PAS.0000000000002345
Sara Petronilho, Elsa Poullot, Axel Andre, Cyrielle Robe, Sako Nouhoum, Virginie Fataccioli, José Miguel Quintela, Alexis Claudel, Josette Brière, Emmanuele Lechapt, François Lemonnier, Rui Henrique, Laurence de Leval, Philippe Gaulard
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引用次数: 0

摘要

T滤泡辅助细胞源淋巴瘤(T-folular helper-cell lymphoma [TFHL])常常伴有B免疫母细胞的扩增,偶尔也会出现霍奇金/里德-斯特恩伯格(HRS)样细胞,因此很难与典型的霍奇金淋巴瘤(CHL)进行鉴别诊断。我们比较了 15 例 TFHL 和 12 例 CHL 样本的形态学、免疫表型和分子特征,并讨论了 4 例诊断不明确的疑难病例。与CHL相比,TFHL更常见于皮层下静脉窦疏松、高端皮层静脉增生、树突状细胞网状结构扩张、T细胞不典型性和T细胞免疫表型异常。HRS样细胞和HRS细胞为CD30+,通常为CD15+和EB病毒感染。这两种疾病都有不同程度的 B 细胞标志物缺失,TFHL 的 HRS 样细胞更常保留 CD20、CD79a、CD19 或 OCT-2 的表达。T细胞浸润主要是CD4+/CD8-,在所有TFHL和75%的CHL中至少有两种TFH标记表达。最有用的 TFH 标记是 CD10(86% 的 TFHL 呈阳性,无 CHL)。12/15的TFHL含有CD30+的肿瘤性TFH细胞,而在CHL中,CD30的表达主要局限于HRS细胞。我们在75%的TFHL中检测到单克隆TR重排,没有发现CHL;在23%的TFHL和42%的CHL中检测到单克隆IG重排。所有TFHL均有TET2突变;13/14例出现RHOA突变,3例伴有DNMT3A突变,1例出现DNMT3A+IDH2突变。3例CHL有TET2突变,可能是克隆造血所致。我们的研究进一步强调,HRS(-like)细胞并不是 CHL 的标志性病变。由于没有单一的病理学标准可以区分TFHL和CHL,因此最好采用包括分子研究在内的综合方法。
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Follicular Helper T-cell Lymphoma With Hodgkin/Reed-Sternberg-Like Cells Versus Classic Hodgkin Lymphoma: A Comparative Study.

Lymphomas of T-follicular helper origin (T-follicular helper-cell lymphoma [TFHL]) are often accompanied by an expansion of B-immunoblasts, occasionally with Hodgkin/Reed-Sternberg-like (HRS-like) cells, making the differential diagnosis with classic Hodgkin lymphoma (CHL) difficult. We compared the morphologic, immunophenotypic, and molecular features of 15 TFHL and 12 CHL samples and discussed 4 challenging cases of uncertain diagnosis. Compared with CHL, TFHL disclosed more frequent sparing of subcortical sinuses, high-endothelium venule proliferation, dendritic cell meshwork expansion, T-cell atypia, and aberrant T-cell immunophenotype. HRS-like and HRS cells were CD30+, often CD15+ and EBV infected. There was a variable loss of B-cell markers in both diseases, with an expression of CD20, CD79a, CD19, or OCT-2 more frequently preserved in HRS-like cells of TFHL. The T-cell infiltrate was predominantly CD4+/CD8-, with expression of at least 2 TFH-markers in all TFHL and 75% of CHL. The most useful TFH marker was CD10 (positive in 86% TFHL and no CHL). Twelve/15 TFHL contained CD30+ neoplastic TFH cells, whereas CD30 expression was mostly restricted to HRS cells in CHL. We detected monoclonal TR rearrangements in 75% of TFHL and no CHL; and monoclonal IG rearrangements in 23% of TFHL and 42% of CHL. All TFHL had TET2 mutations; 13/14 presented RHOA mutations, 3 accompanied by DNMT3A and 1 DNMT3A + IDH2 mutations. Three CHL had TET2 mutations, likely attributable to clonal hematopoiesis. Our study further underlines that HRS(-like) cells are not pathognomonic of CHL. Since no single pathologic criterion distinguishes TFHL and CHL, an integrative approach ideally comprising molecular investigations is fundamental.

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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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