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Cyclin D1-positive diffuse large B-cell lymphoma with IGH-CCND1 translocation and BCL6 rearrangement: a report of two cases.

CyclinD1阳性的弥漫性大B细胞淋巴瘤伴有IGH-CCND1易位及BCL6重排:2例报道

Al-Kawaaz M,Mathew S,Liu Y,Gomez ML,Chaviano F,Knowles DM,Orazi A,Tam W

Abstract

To demonstrate and confirm the existence of cyclin D1-positive diffuse large B-cell lymphoma (DLBCL) with IGH-CCND1 rearrangement and discuss the rationale of differentiating this entity from blastoid and pleomorphic variants of mantle cell lymphoma (MCL).
Two cyclin D1-positive lymphomas with morphologic features of DLBCL and IGH-CCND1 translocations were characterized with respect to clinical features, as well as morphologic, immunophenotypic, cytogenetic, and molecular findings.
The large tumor cells were CD20+, CD5-, CD10-, BCL6+, MUM1+, and cyclin D1+ in both cases. SOX11 was negative. Epstein-Barr virus-encoded RNA in situ hybridization demonstrated diffuse positivity in case 1. BCL6 and IGH-CCND1 rearrangements were identified by fluorescence in situ hybridization in both cases. Specifically, the diagnosis of a relapsed DLBCL with acquisition of IGH-CCND1 was rendered for case 1, molecularly confirmed by the detection of identical monoclonal IGH rearrangements between the initial diagnostic DLBCL and relapse lymphoma.
Our study demonstrates convincingly that IGH-CCND1 rearrangement leading to cyclin D1 overexpression can occur in DLBCL and pose a potential diagnostic pitfall, requiring thorough knowledge of the clinicopathologic findings to allow accurate discrimination from a blastoid or pleomorphic MCL. The coexistence of IGH-CCND1 and IGH-BCL6 rearrangements suggest that BCL6 and cyclin D1 may cooperate in the pathogenesis of DLBCL.

摘要

本文目的是展示和证实CyclinD1+弥漫性大B细胞淋巴瘤伴有IGH-CCND1重排,并讨论这一疾病实体区别于母细胞型和多形性变异型套细胞淋巴瘤的依据。描述两例CyclinD1+、具有DLBCL形态学特征和IGH-CCND1易位淋巴瘤的临床表现、形态学、免疫表型、细胞遗传学和分子结果等方面的特征。两个病例中大的肿瘤细胞均为CD20+、CD5-、CD10-、BCL6+、MUM1+和cyclin D1+,SOX11阴性。病例1的EBER弥漫阳性。两个病例中的BCL6 和 IGH-CCND1重排均通过荧光原位杂交证实。

尤其要注意的是,例1给出的诊断为DLBCL复发伴有IGH-CCND1;分子检测证实,最初诊断的DLBCL和复发的淋巴瘤具有相同的单克隆IGH重组。我们的研究有力的证明DLBCL可以发生IGH-CCND1重排而导致cyclinD1的过表达,从而造成诊断的陷阱。将这类疾病与母细胞型和多形性变异型套细胞淋巴瘤精确的区别开就需要全面了解其临床病理特征。IGH-CCND1重排和IGH-BCL6重排的并存表明BCL6和cyclin D1可能协同参与DLBCL的发病。

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