首页> 美国卫生研究院文献>Internal Medicine >Primary Chest Wall MYC/BCL6 Double-hit Lymphoma with t(3;7)(q27;p12) and t(8;14)(q24;q32) Translocations
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Primary Chest Wall MYC/BCL6 Double-hit Lymphoma with t(3;7)(q27;p12) and t(8;14)(q24;q32) Translocations

机译:t(3; 7)(q27; p12)和t(8; 14)(q24; q32)易位的原发性胸壁MYC / BCL6双重淋巴瘤

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摘要

Primary chest wall lymphoma is rare and typically associated with chronic pleural inflammation. Double-hit lymphoma (DHL), which is defined as aggressive mature B-cell lymphoma with MYC and BCL2 or BCL6 rearrangements, is a highly aggressive malignancy that tends to have extranodal involvement and is resistant to standard immunochemotherapy. We herein report a 55-year-old man with no history of chronic pleural inflammation, diagnosed with primary chest wall DHL with MYC/BCL6 rearrangement, and harboring a unique BCL6 translocation, t(3;7)(q27;p12). After six courses of intensive chemotherapy, he has achieved complete remission. To our knowledge, this is the first case report of primary chest wall DHL.
机译:原发性胸壁淋巴瘤很少见,通常与慢性胸膜炎有关。双发性淋巴瘤(DHL)被定义为具有MYC和BCL2或BCL6重排的侵袭性成熟B细胞淋巴瘤,是一种高度侵袭性恶性肿瘤,倾向于结节外累及,对标准免疫化学疗法有抵抗力。我们在此报告了一个55岁的男性,没有慢性胸膜炎的病史,诊断为原发性胸壁DHL伴有MYC / BCL6重排,并具有独特的BCL6易位,t(3; 7)(q27; p12)。经过六个疗程的强化化疗,他已完全缓解。据我们所知,这是原发性胸壁DHL的首例病例报告。

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