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病例报告:“初治患者中慢性淋巴细胞白血病型单克隆B细胞淋巴细胞增多症向伯基特淋巴瘤的非典型里氏转化”

Case report: 'Atypical Richter transformation from CLL-type monoclonal B-cell lymphocytosis into Burkitt lymphoma in a treatment naïve patient'.

作者信息

Jauch Annaïse J, Alborelli Ilaria, Reusser Andreas, Baschong Albert, Rütsche Cyrill, Bignucolo Olivier, Passweg Jakob, Dirnhofer Stefan, Krasniqi Fatime

机构信息

Division of Medical Oncology, University Hospital of Basel, Basel, Switzerland.

Institute of Medical Genetics & Pathology, Pathology, University Hospital Basel, Basel, Switzerland.

出版信息

Front Oncol. 2024 May 3;14:1296238. doi: 10.3389/fonc.2024.1296238. eCollection 2024.

Abstract

BACKGROUND

Richter transformation refers to the progression of an initially slow-growing small lymphocytic lymphoma/chronic lymphocytic leukemia (SLL/CLL) into an aggressive lymphoma, typically diffuse large B-cell lymphoma (DLBCL) or Hodgkin lymphoma.

CASE PRESENTATION

The patient presented with a rapid onset of localized cervical swelling, accompanied by monoclonal B-cell lymphocytosis displaying a CLL immunophenotype. The histopathological analysis identified a Burkitt lymphoma (BL) located in the submandibular gland and adjacent lymph node. The patient's bone marrow displayed a minor infiltration of monoclonal B-cells with a CLL immunophenotype (< 10%). Molecular analysis demonstrated the presence of the same monoclonal rearrangement in the framework region (FR3 region) of the immunoglobulin heavy chain () locus. High-throughput sequencing of the immunoglobulin heavy and light chains also confirmed the presence of the same rearrangement in SLL/CLL and in the Burkitt lymphoma sample, but also highlighted the presence of a second rearrangement in the Burkitt lymphoma cells, not shared with the SLL/CLL cells in the bone marrow. The patient was treated with DA-EPOCH-R, which lead to a complete metabolic response.

CONCLUSION

This report provides an exceptionally rare description of a CLL-type monoclonal B-cell lymphocytosis transforming into a very aggressive Burkitt lymphoma in a treatment naïve patient.

摘要

背景

里氏转化是指最初生长缓慢的小淋巴细胞淋巴瘤/慢性淋巴细胞白血病(SLL/CLL)进展为侵袭性淋巴瘤,通常为弥漫性大B细胞淋巴瘤(DLBCL)或霍奇金淋巴瘤。

病例介绍

该患者表现为颈部局部迅速肿胀,伴有显示CLL免疫表型的单克隆B细胞淋巴细胞增多症。组织病理学分析确定在颌下腺和相邻淋巴结中有伯基特淋巴瘤(BL)。患者骨髓显示有少量显示CLL免疫表型的单克隆B细胞浸润(<10%)。分子分析表明在免疫球蛋白重链()基因座的框架区(FR3区)存在相同的单克隆重排。免疫球蛋白重链和轻链的高通量测序也证实了SLL/CLL和伯基特淋巴瘤样本中存在相同的重排,但也突出显示伯基特淋巴瘤细胞中存在第二种重排,骨髓中的SLL/CLL细胞未共享这种重排。该患者接受了DA-EPOCH-R治疗,实现了完全代谢缓解。

结论

本报告提供了一个极为罕见的描述,即一名未经治疗的患者中,CLL型单克隆B细胞淋巴细胞增多症转化为极具侵袭性的伯基特淋巴瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4bb/11099200/3fe94b74c525/fonc-14-1296238-g001.jpg

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