Double Hit Lymphoma Mimicking B Cell Precursor Phenotype Burkitt Lymphoma/Leukemia in an Elderly

Takashi Miyoshi, Fumihiko Kono, Yuta Shimazu, Keisuke Shindo, S. Imashuku
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Abstract

Background : The differential diagnosis of Burkitt lymphoma/leukemia (BL) and the double or triple hit lymphomas remains often problematic in terms of immunophenotyping in association with MYC gene analysis. In the past, BL-like B-cell malignancy with B-cell precursor phenotype (BCP-ALL) was described. Case Report : We report here an 84-year-old male with massive ascites without superficial lymphadenopathy. Abdominal paracentesis revealed chylous (non-bloody) ascites consisting of mostly abnormal BL-like blasts showing CD20-negative BCP phenotype. However, molecular study indicated no MYC/IGH , but probable involvements of MYC/IGL and BCL6/IGH translocations, which were confirmed by FISH studies. The patient was diagnosed as double hit lymphoma mimicking BCP-ALL.
双重打击淋巴瘤模拟B细胞前体表型的老年人伯基特淋巴瘤/白血病
背景:在与MYC基因分析相关的免疫表型方面,伯基特淋巴瘤/白血病(BL)和双重或三重命中淋巴瘤的鉴别诊断仍然经常存在问题。在过去,bl样b细胞恶性肿瘤与b细胞前体表型(BCP-ALL)被描述。病例报告:我们在此报告一位84岁男性,有大量腹水,无浅表淋巴结病。腹腔穿刺显示乳糜(无血)腹水,主要由异常bl样细胞组成,显示cd20阴性BCP表型。然而,分子研究表明没有MYC/IGH,但可能涉及MYC/IGL和BCL6/IGH易位,这被FISH研究证实。患者被诊断为模拟BCP-ALL的双发淋巴瘤。
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