Histopathologic Features and Differential Diagnosis in Challenging Cases of Nodular Lymphocyte Predominant B-cell Lymphoma/Nodular Lymphocyte Predominant Hodgkin Lymphoma.

Yanna Ding, Elaine S Jaffe
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Abstract

Nodular lymphocyte predominant Hodgkin lymphoma was termed "nodular lymphocyte predominant B-cell lymphoma" in the International Consensus Classification (ICC), to emphasize clinical and biological differences from classic Hodgkin lymphoma (CHL). The abbreviation "NLP" represents both terms in the ICC and World Health Organization classifications. Variations in the growth pattern, originally reported as Fan patterns A-F, are designated as either grade 1 or grade 2 in the ICC. NLP is uncommon, and in some cases an accurate diagnosis is challenging. The objectives of this article were to review the histopathologic features of NLP and the differential diagnosis from other key entities including de novo T-cell/histiocyte-rich large B-cell lymphoma (THRLBL) and lymphocyte-rich classic Hodgkin lymphoma (LRCHL). Histologically, NLP Fan pattern E (THRLBL-like) can be indistinguishable from de novo THRLBL. However, focal nodular areas, clustering of tumor cells, presence of few admixed small B-cells or FDC meshworks, and T-cell rosettes favor NLP Fan pattern E and argue against de novo THRLBL. NLP may also be confused with LRCHL. Patients with NLP are younger than those with LRCHL, and LRCHL may show mediastinal involvement. In LRCHL, the nodular pattern often contains eccentrically located small regressed germinal centers and intact small dense FDC meshworks, in contrast to the expanded, and fragmented FDC meshworks in NLP. Neoplastic cells that are positive for CD30 and CD15 but negative for CD20 and CD79a are characteristic of LRCHL. Additionally, Fascin and Gata3 are commonly positive in LRCHL but usually negative in NLP.

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结节性淋巴细胞为主的 B 细胞淋巴瘤/结节性淋巴细胞为主的霍奇金淋巴瘤疑难病例的组织病理学特征和鉴别诊断。
结节性淋巴细胞占优势的霍奇金淋巴瘤在国际共识分类(ICC)中被称为 "结节性淋巴细胞占优势的B细胞淋巴瘤",以强调与典型霍奇金淋巴瘤(CHL)在临床和生物学上的差异。缩写 "NLP "代表了 ICC 和世界卫生组织分类中的两个术语。生长模式的变异最初被报告为 Fan 模式 A-F,在 ICC 中被定为 1 级或 2 级。NLP 并不常见,在某些情况下,准确诊断具有挑战性。本文旨在回顾NLP的组织病理学特征,以及与其他重要实体的鉴别诊断,包括新生T细胞/组织细胞丰富的大B细胞淋巴瘤(THRLBL)和淋巴细胞丰富的典型霍奇金淋巴瘤(LRCHL)。组织学上,NLP Fan 模式 E(THRLBL-like)与新生 THRLBL 无法区分。然而,局灶性结节区、肿瘤细胞聚集、存在少量混杂的小B细胞或FDC网状细胞以及T细胞花环都有利于NLP Fan模式E,而不利于新生THRLBL。NLP也可能与LRCHL混淆。NLP患者比LRCHL患者年轻,而LRCHL患者可能会出现纵隔受累。在LRCHL中,结节形态通常包含位于偏心位置的小的退行性生发中心和完整的小的致密的FDC网状结构,而在NLP中,FDC网状结构则会扩张和破碎。CD30 和 CD15 阳性但 CD20 和 CD79a 阴性的肿瘤细胞是 LRCHL 的特征。此外,Fascin 和 Gata3 在 LRCHL 中通常呈阳性,但在 NLP 中通常呈阴性。
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Histopathologic Features and Differential Diagnosis in Challenging Cases of Nodular Lymphocyte Predominant B-cell Lymphoma/Nodular Lymphocyte Predominant Hodgkin Lymphoma. A Review and Update on Therapy of Gastrointestinal Tract Tumors: From the Bench to Clinical Practice Updates from the 2022 WHO Classification of Kidney Epithelial Tumors Disseminated Carcinomatosis of Bone Marrow with or without an Unknown Primary Site: A Case Series Atypia of Undetermined Significance in Thyroid Fine Needle Aspiration Cytology Revisited
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