Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ann Diagn Pathol. 2024 Dec;73:152372. doi: 10.1016/j.anndiagpath.2024.152372. Epub 2024 Aug 22.
Composite lymphoma, defined as two or more distinct well-defined entities involving the same anatomic site, is rare. Here we report a 79-year-old woman with composite mantle cell lymphoma (MCL) and lymphoplasmacytic lymphoma (LPL) involving bone marrow at the time of initial diagnosis. The patient presented with splenomegaly and lymphadenopathy and laboratory studies showed an elevated serum IgM level and IgM kappa paraprotein. Bone marrow evaluation showed concurrent involvement by MCL and LPL, supported by immunophenotypic studies that revealed two distinct aberrant B-cell populations. Next-generation sequencing analysis identified concurrent MYD88 and CXCR4 mutations and fluorescence in-situ hybridization showed CCND1 translocation, supporting the diagnosis of concomitant MCL and LPL. In conclusion, composite lymphoma can present in the bone marrow. The use of ancillary studies was essential in reaching the diagnosis in this case, as the results excluded the possibility of MCL lymphoma with plasmacytic differentiation, as well as other CD5- and CD10-negative small B-cell lymphomas.
复合淋巴瘤定义为累及同一解剖部位的两种或两种以上明确的不同实体,较为罕见。在此,我们报告了一例 79 岁女性,初诊时即患有累及骨髓的复合套细胞淋巴瘤(MCL)和淋巴浆细胞淋巴瘤(LPL)。该患者表现为脾肿大和淋巴结病,实验室研究显示血清 IgM 水平和 IgM κ 副蛋白升高。骨髓评估显示 MCL 和 LPL 同时受累,免疫表型研究显示存在两种不同的异常 B 细胞群,进一步支持这一诊断。下一代测序分析发现同时存在 MYD88 和 CXCR4 突变,荧光原位杂交显示 CCND1 易位,支持同时患有 MCL 和 LPL 的诊断。总之,复合淋巴瘤可发生于骨髓。在本例中,辅助研究的应用对明确诊断至关重要,因为这些结果排除了 MCL 伴浆细胞分化以及其他 CD5-和 CD10-阴性小 B 细胞淋巴瘤的可能性。