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同一患者同时存在弥漫性大B细胞淋巴瘤、急性髓系白血病和未经治疗的淋巴浆细胞性淋巴瘤/华氏巨球蛋白血症:一例报告。

Coexistence of diffuse large B-cell lymphoma, acute myeloid leukemia, and untreated lymphoplasmacytic lymphoma/waldenström macroglobulinemia in a same patient: A case report.

作者信息

Zhang Liu-Bo, Zhang Lu, Xin Hong-Lei, Wang Yan, Bao Hong-Yu, Meng Qing-Qi, Jiang Su-Yu, Han Xue, Chen Wan-Ru, Wang Jian-Ning, Shi Xiao-Feng

机构信息

Department of Hematology, Second Affiliated Hospital of Nanjing Medical University, Nanjing 210003, Jiangsu Province, China.

Department of Pathology, Second Affiliated Hospital of Nanjing Medical University, Nanjing 210003, Jiangsu Province, China.

出版信息

World J Clin Cases. 2023 Jun 26;11(18):4295-4305. doi: 10.12998/wjcc.v11.i18.4295.

Abstract

BACKGROUND

The Coexistence of myeloid and lymphoid malignancies is rare. Myeloid leukemia occurs more frequently as a secondary event in patients receiving chemotherapy agents for lymphoid malignancies. Synchronous diagnoses of diffuse large B-cell lymphoma (DLBCL), acute myeloid leukemia (AML), and untreated lymphoplasmacytic lymphoma/Waldenström macroglobulinemia (LPL/WM) in the same patient have not been reported. Here we report one such case.

CASE SUMMARY

An 89-year-old man had a chest wall mass histopathologically diagnosed as DLBCL. The bone marrow and peripheral blood contained two groups of cells. One group of cells fulfilled the criteria of AML, and the other revealed the features of small B lymphocytic proliferative disorder, which we considered LPL/WM. Multiple chromosomal or genetic changes were detected in bone marrow mononuclear cells, including deletion, amplification, mutations of (L265P) and , overexpression, and fusion gene of , as well as complex chromosomal abnormalities. The patient refused chemotherapy because of old age and died of pneumonia 1 mo after the final diagnosis.

CONCLUSION

The coexistence of DLBCL, AML, and untreated LPL/WM in the same patient is extremely rare, which probably results from multiple steps of genetic abnormalities. Asymptomatic LPL/WM might have occurred first, then myelodysplastic syndrome-related AML developed, and finally aggressive DLBCL arose. Therefore, medical staff should pay attention to this rare phenomenon to avoid misdiagnoses.

摘要

背景

髓系和淋巴系恶性肿瘤共存的情况较为罕见。在接受淋巴系恶性肿瘤化疗药物治疗的患者中,髓系白血病作为继发事件更为常见。同一患者同时诊断为弥漫性大B细胞淋巴瘤(DLBCL)、急性髓系白血病(AML)和未经治疗的淋巴浆细胞淋巴瘤/华氏巨球蛋白血症(LPL/WM)的情况尚未见报道。在此我们报告这样一例病例。

病例摘要

一名89岁男性胸部有一肿块,经组织病理学诊断为DLBCL。骨髓和外周血中有两组细胞。一组细胞符合AML的标准,另一组显示小B淋巴细胞增殖性疾病的特征,我们认为是LPL/WM。在骨髓单个核细胞中检测到多种染色体或基因改变,包括缺失、扩增、(L265P)和的突变、过表达以及的融合基因,还有复杂的染色体异常。患者因年龄较大拒绝化疗,最终诊断后1个月死于肺炎。

结论

同一患者中DLBCL、AML和未经治疗的LPL/WM共存极为罕见,这可能是由多个基因异常步骤导致的。无症状的LPL/WM可能首先发生,然后发展为骨髓增生异常综合征相关的AML,最后出现侵袭性DLBCL。因此,医务人员应注意这种罕见现象以避免误诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180a/10336997/d97e0d2c6add/WJCC-11-4295-g001.jpg

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