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原发性CD56 +鼻型T/自然杀伤细胞皮下脂膜炎样淋巴瘤:表现为噬血细胞综合征。

Primary CD56 + nasal-type T/natural killer-cell subcutaneous panniculitic lymphoma: presentation as haemophagocytic syndrome.

作者信息

Jang K A, Choi J H, Sung K J, Moon K C, Koh J K, Kwon Y M, Chi H S

机构信息

Department of Dermatology, Asan Medical Centre, College of Medicine, University of Ulsan, Seoul, Korea.

出版信息

Br J Dermatol. 1999 Oct;141(4):706-9. doi: 10.1046/j.1365-2133.1999.03114.x.

Abstract

Natural killer (NK) cells are large granular lymphocytes that mediate cytotoxic reactions which are not restricted by the major histocompatibility complex. In recent years it has become apparent that a minor proportion of malignant lymphomas expresses an NK-cell phenotype defined by its reactivity with the CD56 antibody. Primary purely cutaneous CD56 + lymphomas have rarely been reported. They share a generally aggressive course and are highly associated with Epstein-Barr virus. We describe a patient with a primary cutaneous nasal-type T/NK-cell lymphoma that presented as a haemophagocytic syndrome and showed an aggressive clinical course.

摘要

自然杀伤(NK)细胞是大颗粒淋巴细胞,介导不受主要组织相容性复合体限制的细胞毒性反应。近年来,已明显发现一小部分恶性淋巴瘤表达由其与CD56抗体反应所定义的NK细胞表型。原发性单纯皮肤CD56 +淋巴瘤鲜有报道。它们通常病程侵袭性强,且与爱泼斯坦-巴尔病毒高度相关。我们描述了一名原发性皮肤鼻型T/NK细胞淋巴瘤患者,该患者表现为噬血细胞综合征,临床病程呈侵袭性。

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