The Spectrum of B-cell and Plasma Cell Proliferations in Nodal T Follicular Helper Cell Lymphomas.

IF 4.5 1区 医学 Q1 PATHOLOGY American Journal of Surgical Pathology Pub Date : 2024-12-02 DOI:10.1097/PAS.0000000000002340
Roman Segura-Rivera, Nicholas Joseph Dcunha, Yiannis Petros Dimopoulos, Aniruddha Mundhada, Tania P Sainz, Claudia Kettlun, Vishal Sahu, Iman Sarami, Roberto N Miranda, Pei Lin, Leonard Jeffrey Medeiros, Francisco Vega
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Abstract

B-cell and plasma cell proliferations are frequently observed in nodal T follicular helper (nTfh) cell lymphomas and can present a diagnostic challenge. These proliferations can be monotypic or monoclonal and morphologically resemble lymphoma or plasmacytoma, but their clinical behavior is poorly defined. In this study, we reviewed 414 cases of nTfh lymphoma seen over the past decade at our institution. We identified 78 (19%) cases that exhibited B-cell or plasma cell proliferation detected by morphology, flow cytometry, immunohistochemistry, and/or molecular techniques. The B-cell/plasma cell proliferations occurred before (22%), concurrently with (50%), or after (28%) the diagnosis of nTfh lymphoma. We divided them into 3 categories: (1) focal or scattered B-immunoblastic proliferations recognized morphologically without a monotypic/monoclonal B-cell population (17%), (2) monotypic/monoclonal B-cell/plasma cells identified solely by flow cytometry or molecular clonality studies without morphologic confirmation (11%), and (3) unequivocal B-cell/plasma cell expansions recognized by morphologic assessment (72%). We further subdivided group 3 into proliferations associated with and possibly dependent on neoplastic Tfh cells versus those proliferations occurring in the absence of neoplastic Tfh cells and likely bona fide lymphomas. Follow-up biopsy specimens showed persistence of B-cell/plasma cell proliferations in various patient subcategories, with transformation to higher-grade B-cell proliferation or persistence without Tfh cells in some cases. In conclusion, our data support the notion that most B-cell and plasma cell proliferations associated with neoplastic Tfh clones have little impact on the clinical course of patients with nTfh lymphoma and likely do not constitute an independent B-cell lymphoma, especially those of small B cells of plasma cells. However, B-cell expansions exhibiting aggressive morphologic features may represent an independent B-cell lymphoma.

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b细胞和浆细胞在淋巴结T滤泡辅助细胞淋巴瘤中的增殖谱。
b细胞和浆细胞增生在淋巴结T滤泡辅助细胞(nTfh)淋巴瘤中经常观察到,这可能是一个诊断挑战。这些增生可以是单型或单克隆的,在形态上类似于淋巴瘤或浆细胞瘤,但其临床行为尚不清楚。在这项研究中,我们回顾了过去十年来在我们机构看到的414例nTfh淋巴瘤。通过形态学、流式细胞术、免疫组织化学和/或分子技术检测,我们发现78例(19%)患者表现出b细胞或浆细胞增殖。b细胞/浆细胞增生发生在诊断nTfh淋巴瘤之前(22%)、同时(50%)或之后(28%)。我们将它们分为3类:(1)局灶性或分散的b免疫母细胞增殖,形态学上可以识别,但没有单型/单克隆b细胞群(17%);(2)单型/单克隆b细胞/浆细胞,仅通过流式细胞术或分子克隆研究识别,但没有形态学确认(11%);(3)通过形态学评估识别的明确的b细胞/浆细胞扩增(72%)。我们进一步将第3组细分为与肿瘤Tfh细胞相关并可能依赖于肿瘤Tfh细胞的增殖,以及在没有肿瘤Tfh细胞和可能是真正的淋巴瘤的情况下发生的增殖。随访活检标本显示,在不同的患者亚类别中,b细胞/浆细胞增殖持续存在,在某些病例中,转化为更高级别的b细胞增殖或不含Tfh细胞的持续存在。总之,我们的数据支持这样的观点,即大多数与肿瘤性Tfh克隆相关的B细胞和浆细胞增殖对nTfh淋巴瘤患者的临床病程影响不大,可能不构成独立的B细胞淋巴瘤,尤其是浆细胞中的小B细胞。然而,表现出侵袭性形态特征的b细胞扩增可能代表一种独立的b细胞淋巴瘤。
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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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