克隆相关结节性弥漫大B细胞淋巴瘤和心包积液弥漫大B细胞淋巴瘤伴MYD88 L265P突变的汉斯标准不一致。

IF 0.9 Q4 HEMATOLOGY
Toshiki Terao, Yumiko Sato, Yoshiaki Kuroda, Tomoka Haratake, Midori Filiz Nishimura, Yasuharu Sato, Shoichi Kuyama
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引用次数: 0

摘要

一名 79 岁的日本妇女因劳累性呼吸困难前来就诊。她患有心脏压塞,医生紧急为她进行了心包引流术。心包积液的病理结果显示为非生殖中心B细胞(non-GCB)心包大B细胞淋巴瘤(CD10-、BCL6+和MUM1+)。虽然考虑了体液过多相关大B细胞淋巴瘤的诊断,但通过对肿大的左侧腋窝淋巴结进行针刺活检,发现了GCB结弥漫大B细胞淋巴瘤(CD10+、BCL6+和MUM1+)。尽管这两种淋巴瘤的 CD10 表达水平不同,但聚合酶链反应评估 IgH 基因重排表明它们之间存在克隆关系。此外,通过桑格测序证实了两个样本中都存在MYD88 L265P突变,提示为MCD型。我们的病例凸显了汉斯标准与基于基因表达谱的起源细胞之间的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discrepancy of Hans' criteria for clonally related nodal and pericardiac fluid diffuse large B-cell lymphoma with MYD88 L265P mutation.

A 79-year-old Japanese woman presented with exertional dyspnea. She had cardiac tamponade and urgent pericardial drainage was performed. Pathological findings from the pericardial fluid revealed non-germinal center B-cell (non-GCB) pericardial large B-cell lymphoma (CD10-, BCL6+, and MUM1+). Although a diagnosis of fluid overload-associated large B-cell lymphoma was considered, GCB nodal diffuse large B-cell lymphoma (CD10+, BCL6+, and MUM1+) was discovered through needle biopsy of the enlarged left axillary lymph node. Despite the two lymphomas exhibiting different expression levels of CD10, polymerase chain reaction assessing IgH gene rearrangement suggested a clonal relationship between them. Additionally, MYD88 L265P mutation was confirmed using Sanger sequencing in both samples, suggesting the MCD type. Our case highlights a discrepancy between the Hans' criteria and the gene expression profile-based cell of origin.

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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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