A Rare Case of Richter Transformation to Both Clonally Unrelated and Clonally Related Diffuse Large B-Cell Lymphoma in the Same Patient.

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2024-08-31 eCollection Date: 2024-01-01 DOI:10.1155/2024/7913296
Michelle D Don, Carlos Casiano, Huan-You Wang, Mikhail Gorbounov, Wei Song, Edward D Ball
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Abstract

Richter transformation (RT) is a rare sequelae of chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). The clonal relationship of the RT to the underlined CLL/SLL is an important prognostic factor as clonally related RT has a worse prognosis than that of clonally unrelated RT. The development of more than one RT in the same patient is exceedingly rare and prior reports have shown cases consisting of RT to diffuse large B-cell lymphoma (DLBCL) and a subsequent or synchronous Hodgkin lymphoma. Here, we present a rare case of RT first to a clonally unrelated DLBCL and subsequently a clonally related DLBCL. Additionally, we retrospectively conducted next-generation sequencing studies of both RT's and found different mutational landscapes, including more clinically aggressive mutations identified in the clonally related RT. To our knowledge, this is the first reported case of clonally related and clonally unrelated RT, both of which are DLBCL, in the same patient.

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罕见的同一名患者同时发生里氏转化为克隆无关和克隆相关的弥漫大 B 细胞淋巴瘤病例
里克特转化(RT)是慢性淋巴细胞白血病(CLL)/小淋巴细胞淋巴瘤(SLL)的一种罕见后遗症。RT与下划线CLL/SLL的克隆关系是一个重要的预后因素,因为克隆相关的RT比克隆无关的RT预后更差。在同一患者身上发生不止一种RT的情况极为罕见,之前的报告显示,有的病例是弥漫大B细胞淋巴瘤(DLBCL)发生RT,随后又发生或同步发生霍奇金淋巴瘤。在这里,我们介绍了一例罕见病例,患者先是接受了与克隆无关的 DLBCL 的 RT 治疗,随后又接受了克隆相关的 DLBCL 治疗。此外,我们回顾性地对两例RT进行了新一代测序研究,发现了不同的突变景观,包括在与克隆相关的RT中发现的更具临床侵袭性的突变。据我们所知,这是首例报道的同一患者同时患有克隆相关和克隆无关RT(均为DLBCL)的病例。
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审稿时长
13 weeks
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