MYD88突变阳性、中枢神经系统受累的轻度B细胞淋巴瘤:Bing-Neel综合征模仿者

IF 0.9 Q4 HEMATOLOGY
Kenichiro Takeda, Shoichiro Okazaki, Rintaro Minami, Akihumi Ichiki, Yusuke Yamaga, Kosei Nakajima, Kunio Kitamura, Kennosuke Karube, Takahiro Nishiyama
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引用次数: 0

摘要

90% 以上的瓦尔登斯特伦巨球蛋白血症(WM)患者存在 MYD88 p.L265P 突变,其特征是淋巴浆细胞性淋巴瘤(LPL)伴单克隆 IgM。由于 WM 与其他 B 细胞恶性肿瘤的特征重叠,因此需要仔细诊断。Bing-Neel综合征(BNS)是WM的一种罕见并发症,涉及中枢神经系统(CNS)的侵犯。本报告描述了两例骨髓中形态学上的低级别 B 细胞淋巴瘤,同时伴有脑中的大 B 细胞淋巴瘤和常见的 MYD88 p.L265P 突变,这两例病例最终被确定为 BNS 拟态患者。虽然这些病例中的两种成分显示出相同的轻链限制,但不同的免疫球蛋白重链重排峰表明中枢神经系统和骨髓病变的淋巴瘤干细胞各不相同。这些临床病例强调了诊断 BNS 所面临的挑战。根据研究结果,建议进行活组织检查,以准确确定克隆关系和 MYD88 基因突变状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MYD88 mutation-positive indolent B-cell lymphoma with CNS involvement: Bing-Neel syndrome mimickers.

MYD88 p.L265P mutation occurs in over 90% of Waldenström's macroglobulinemia (WM), which is characterized by lymphoplasmacytic lymphoma (LPL) with monoclonal IgM. WM requires careful diagnosis due to overlapping features with other B-cell malignancies. Bing-Neel syndrome (BNS), a rare complication of WM, involves central nervous system (CNS) invasion. This report describes two cases of morphologically low-grade B-cell lymphoma in the bone marrow accompanied by the presence of a large B-cell lymphoma in the brain and a common MYD88 p.L265P mutation, which were eventually established as BNS mimickers. Although the two components in these cases showed the same identical light-chain restriction, different immunoglobulin heavy-chain rearrangement peaks indicated distinct lymphoma stem cells for CNS and bone marrow lesions. These clinical cases emphasize the challenges in diagnosing BNS. Based on the findings, biopsy is recommended for accurate identification of the clonal relationship and MYD88 mutation status.

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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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