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皮肤型里希特综合征:更好的转化部位?

Cutaneous Richter syndrome: a better place to transform?

机构信息

Skin Tumour Unit, 2nd Floor, Block C, South Wing, St. John's Institute of Dermatology, St Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, U.K.

出版信息

Br J Dermatol. 2015 Feb;172(2):513-21. doi: 10.1111/bjd.13193. Epub 2014 Dec 30.

Abstract

The development of high-grade lymphoma in patients with chronic lymphocytic leukaemia is known as Richter syndrome (RS) and is associated with a grave prognosis, with a mean survival of 8 months despite treatment. Cutaneous RS has been described in a handful of cases and may be associated with a better outcome than the more common extracutaneous variants. We review the literature with particular emphasis on pathogenesis, treatment and survival of RS. We postulate that the absence of B symptoms and a normal lactate dehydrogenase level, presumably reflecting localized or limited disease, and a lower tumour burden, may explain the apparently better survival in some patients with cutaneous RS than with extracutaneous variants.

摘要

慢性淋巴细胞白血病患者中高级别淋巴瘤的发展称为里希特综合征(RS),并与预后不良相关,尽管进行了治疗,但平均生存时间仍为 8 个月。已经描述了少数皮肤 RS 病例,并且与更常见的皮肤外变体相比,可能与更好的结果相关。我们特别强调 RS 的发病机制、治疗和生存情况来审查文献。我们推测,缺乏 B 症状和正常的乳酸脱氢酶水平(可能反映局部或局限性疾病)以及较低的肿瘤负担,可能解释了一些皮肤 RS 患者比皮肤外变体的生存时间明显更长的原因。

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