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以噬血细胞性淋巴组织细胞增生症为首发表现并伴有淋巴细胞消减的霍奇金淋巴瘤:一例报告及文献复习

Lymphocyte-depleted Hodgkin lymphoma complicating hemophagocytic lymphohistiocytosis as an initial manifestation: a case report and review of the literature.

作者信息

Hagihara Masao, Inoue Morihiro, Hua Jian, Iwaki Yasunobu

机构信息

Department of Hematology, Eiju General Hospital, Japan.

出版信息

Intern Med. 2012;51(21):3067-72. doi: 10.2169/internalmedicine.51.8275. Epub 2012 Nov 1.

Abstract

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.

摘要

噬血细胞性淋巴组织细胞增生症(HLH)通常与感染性疾病或T/NK细胞淋巴瘤相关;然而,与霍奇金淋巴瘤(HL)相关的情况鲜有报道。在此,我们描述了一名年轻男性,其最初表现为诊断为淋巴细胞消减型HL(LD-HL)并伴有HLH。他接受了大剂量类固醇治疗加重组血栓调节蛋白治疗,随后接受ABVd(阿霉素、博来霉素、长春花碱、达卡巴嗪)治疗。尽管经过一个周期的ABVd治疗实现了部分缓解,但他在3个周期后复发。据我们所知,本病例非常罕见,可能需要更强化的治疗来长期控制HLH合并HL。

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