霍奇金淋巴瘤与非霍奇金淋巴瘤的共存混合性淋巴瘤(CL)患者表现为淋巴结肿大和减弱。

E. Geladari, G. Dimopoulou, E. Margellou, Andreas Paraskevas, G. Kafetzis, D. Rontogianni, M. Vadiaka
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引用次数: 3

摘要

背景:在同一器官内同时诊断两种或两种以上类型的淋巴瘤被定义为复合淋巴瘤,这是一种最近在文献中发现的罕见疾病(1)。值得注意的是,同时发生的可能是霍奇金淋巴瘤与非霍奇金淋巴瘤(NHL)的B细胞或T细胞,或两种不同的NHL实体。此外,这种情况已被同时或依次描述(2)。为了确定诊断,应该通过形态学和实验室检查证实两个或多个不同的克隆(3)。病例介绍:我们引用了一位73岁的女性患者,她表现为低烧,颈淋巴肿大和颈淋巴肿大,其腋窝淋巴结活检显示罕见的霍奇金淋巴瘤和非霍奇金淋巴瘤共存,称为复合淋巴瘤。结论:复合性淋巴瘤具有特殊的诊断挑战性,目前尚无一致的治疗标准(4)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coexistence of Hodgkin and Non-Hodgkin lymphoma; Composite Lymphoma (CL) in a patient presenting with waxing and waning lymphadenopathy.
BACKGROUND The coexistence of two or more types of lymphoma within the same organ at the same time of diagnosis is defined as composite lymphoma, a rare disease that has recently been identified in the literature (1). Pointedly, the concurrence may be Hodgkin lymphoma with a Non-Hodgkin lymphoma (NHL) either B or T cells, or two different entities of NHLs. Furthermore, this condition has been described concurrently or sequentially (2). In order for the diagnosis to be established, two or more distinct clones should be proven by morphological and laboratory tests (3). Case presentation: Herein, we cite a seventy-three-years old female patient who presented with low-grade fever, waxing and waning cervical lymphadenopathy, whose biopsy of an axillary lymph node demonstrated the rare coexistence of Hodgkin and NHL, known as composite lymphoma. Conclusion: Composite lymphomas pose a particular diagnostic challenge, and currently there are no agreed standards for treatment (4).
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