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首页> 外文期刊>Internal medicine. >Lymphocyte-depleted Hodgkin Lymphoma Complicating Hemophagocytic Lymphohistiocytosis as an Initial Manifestation: A Case Report and Review of the Literature
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Lymphocyte-depleted Hodgkin Lymphoma Complicating Hemophagocytic Lymphohistiocytosis as an Initial Manifestation: A Case Report and Review of the Literature

机译:淋巴细胞减少的霍奇金淋巴瘤并发吞噬性淋巴细胞组织细胞增多症为最初表现:一例病例并文献复习

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Hemophagocytic lymphohistocytosis (HLH) is commonly associated with infectious diseases or T/NK cell-lymphoma; however that with Hodgkin lymphoma (HL) was rarely reported. Herein, we describe a young male diagnosed with lymphocyte-depleted HL (LD-HL) complicated by HLH as an initial manifestation. He was given high-dose steroid therapy plus recombinant thrombomodulin, and subsequent ABVd (doxorubicin, bleomycin, vinblastine, dacarbazine) treatment. In spite of the achievement of a partial remission treated with one cycle of ABVd, he relapsed after 3 cycles. To our knowledge, the present case is very rare, and more intensive treatment might be needed for the long-term control of HLH-complicated HL.
机译:吞噬性淋巴细胞组织细胞增生症(HLH)通常与传染病或T / NK细胞淋巴瘤相关;然而,关于霍奇金淋巴瘤(HL)的报道很少。在本文中,我们描述了一名年轻男性,被诊断为伴有HLH的淋巴细胞耗竭性HL(LD-HL)作为初始表现。他接受了大剂量的类固醇疗法加重组血栓调节蛋白治疗,随后接受了ABVd(阿霉素,博来霉素,长春碱,达卡巴嗪)治疗。尽管通过一个周期的ABVd治疗可部分缓解,但他在3个周期后复发。据我们所知,本病例非常罕见,长期控制HLH并发HL可能需要更深入的治疗。

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