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皮肤B细胞淋巴瘤

Cutaneous B-cell lymphoma.

作者信息

Burg G, Kaudewitz P, Klepzig K, Przybilla B, Braun-Falco O

出版信息

Dermatol Clin. 1985 Oct;3(4):689-704.

PMID:3916175
Abstract

The various morphologic and functional subtypes of nodal B-cell lymphomas can also be found in the skin. These reflect the various steps of lymphocyte differentiation including maturation from the pre-B lymphocyte to the well-differentiated B2 lymphocyte or plasma cell in the peripheral blood. The subtypes of cutaneous B-cell lymphomas have been discussed (Kiel classification); the percentages indicate the frequencies of the subtypes among a total of 736 cutaneous lymphomas of both T-cell and B-cell origin: Lymphocytic lymphoma (7 per cent). Immunoglobulin-producing lymphomas, including the rate plasmacytoma of the skin, lymphoplasmacytoid immunocytoma, which represents the largest group of cutaneous B-cell lymphoma (12 per cent), and immunoblastic lymphoma, which is the most aggressive form in this group (8 per cent). Cutaneous B-cell lymphoma arising from or related to follicular center cells, including centrocytic lymphoma (7 per cent), mantle-cell lymphoma, centroblastic/centrocytic lymphoma (6 per cent), the highly malignant centroblastic lymphoma (4 per cent), and lymphoblastic lymphoma, Burkitt type. The Ann Arbor staging system is not applicable to cutaneous B-cell lymphoma; therefore, a TNM staging system has been proposed. The diagnosis of cutaneous B-cell lymphoma is based primarily on cytomorphologic features. Differentiation of cutaneous B-cell lymphoma from pseudolymphoma of the skin cannot be based on a single criterion; a spectrum of characteristic features must be evaluated. Analysis of the infiltrating cells in cutaneous B-cell lymphoma using monoclonal antibodies demonstrates that the proliferation of the neoplastic clone is accompanied by a mixture of accessory cells of various origins, including T cells, macrophages, and dendritic reticulum cells. As in nodal B-cell lymphomas, several factors may be involved in the generation of cutaneous B-cell lymphoma, including persistent antigenic stimulation and loss of regulatory mechanisms for lymphocyte proliferation and differentiation in conjunction with environmental and other factors.

摘要

淋巴结B细胞淋巴瘤的各种形态学和功能亚型在皮肤中也可出现。这些反映了淋巴细胞分化的各个阶段,包括从前B淋巴细胞在外周血中成熟为分化良好的B2淋巴细胞或浆细胞。皮肤B细胞淋巴瘤的亚型已被讨论过(基尔分类法);百分比表示这些亚型在总共736例T细胞和B细胞起源的皮肤淋巴瘤中的发生率:淋巴细胞淋巴瘤(7%)。产生免疫球蛋白的淋巴瘤,包括皮肤浆细胞瘤、淋巴浆细胞样免疫细胞瘤(它是皮肤B细胞淋巴瘤中最大的一组,占12%)以及免疫母细胞淋巴瘤(它是该组中最具侵袭性的形式,占8%)。起源于滤泡中心细胞或与之相关的皮肤B细胞淋巴瘤,包括中心细胞性淋巴瘤(7%)、套细胞淋巴瘤、中心母细胞/中心细胞性淋巴瘤(6%)、高度恶性的中心母细胞淋巴瘤(4%)以及伯基特型淋巴母细胞淋巴瘤。安阿伯分期系统不适用于皮肤B细胞淋巴瘤;因此,有人提出了一种TNM分期系统。皮肤B细胞淋巴瘤的诊断主要基于细胞形态学特征。皮肤B细胞淋巴瘤与皮肤假性淋巴瘤的鉴别不能基于单一标准;必须评估一系列特征。使用单克隆抗体分析皮肤B细胞淋巴瘤中的浸润细胞表明,肿瘤克隆的增殖伴随着多种来源的辅助细胞的混合,包括T细胞、巨噬细胞和树突状网状细胞。与淋巴结B细胞淋巴瘤一样,皮肤B细胞淋巴瘤的发生可能涉及多种因素,包括持续的抗原刺激以及淋巴细胞增殖和分化调节机制的丧失,同时还伴有环境和其他因素。

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Cutaneous B-cell lymphoma.皮肤B细胞淋巴瘤
Dermatol Clin. 1985 Oct;3(4):689-704.

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