University of Pennsylvania Philadelphia, PA 19104, USA.
G Ital Dermatol Venereol. 2010 Jun;145(3):361-73.
Primary cutaneous B-cell lymphomas (PCBCL) represent a heterogeneous group of lymphoproliferative disorders characterized by clonal proliferation of neoplastic B-cells in the skin. The recent joint World Health Organization (WHO) and European Organization for the Research and Treatment of Cancer (EORTC) classification recognizes three major subgroups of PCBCL: primary cutaneous follicle center lymphoma (PCFCL), primary cutaneous marginal zone B-cell lymphoma (PCMZL) and primary cutaneous large B-cell lymphoma, leg type (PCLBCL-LT). Recent advances in the field and the availability of new methodological tools have greatly enhanced our insights into the biology of cutaneous B-cell lymphomas and allow a more precise definition of these entities. Considerable progress over the past decade has led to significantly improved diagnostic accuracy allowing earlier diagnosis, targeted strategies and improved therapeutic results in the management of primary cutaneous B-cell lymphomas. This review presents an overview of primary cutaneous B-cell lymphomas with an emphasis on the proper incorporation of current and emerging diagnostic tools into the work-up and classification of this group of unique malignancies.
原发性皮肤 B 细胞淋巴瘤(PCBCL)是一组异质性的淋巴增殖性疾病,其特征为皮肤中肿瘤性 B 细胞的克隆性增殖。最近,世界卫生组织(WHO)和欧洲癌症研究与治疗组织(EORTC)联合分类将 PCBCL 分为三个主要亚组:原发性皮肤滤泡中心淋巴瘤(PCFCL)、原发性皮肤边缘区 B 细胞淋巴瘤(PCMZL)和原发性皮肤大 B 细胞淋巴瘤,腿型(PCLBCL-LT)。该领域的最新进展和新方法学工具的出现极大地增强了我们对皮肤 B 细胞淋巴瘤生物学的认识,并能够更精确地定义这些实体。过去十年的重大进展导致诊断准确性显著提高,这使得在原发性皮肤 B 细胞淋巴瘤的管理中能够更早地诊断、采取靶向策略并获得更好的治疗效果。本文重点介绍了皮肤 B 细胞淋巴瘤的正确诊断和分类,强调了将当前和新兴的诊断工具纳入这组独特恶性肿瘤的评估和分类中。