Dummer R, Potoczna N, Häffner A C, Zimmermann D R, Gilardi S, Burg G
Department of Dermatology, University of Zürich, Switzerland.
Arch Dermatol. 1996 May;132(5):550-3.
Cutaneous lymphomas are heterogeneous clonal lymphoproliferative disorders originating from B or T lymphocytes.
We describe a patient with a unique primary cutaneous lymphoma characterized by a bruise-like aspect of the skin lesions, a CD4+, CD43+, CD56+, CD2-, CD3-, CD8-, T-cell receptor-negative phenotype of the medium-sized to large lymphoid tumor cells and an undetermined genotype (T-cell receptor beta and immunoglobulin heavy chain in germline configuration, no clonal T-cell receptor gamma population as detected after analysis with polymerase chain reaction combined with denaturing gradient gel electrophoresis) and fast relapse after radiotherapy.
This non-B, non-T cutaneous lymphoma cannot be classified by any current lymphoma classification. It seems to represent a new disease entity with peculiar clinical, histologic, and molecular features.
皮肤淋巴瘤是起源于B或T淋巴细胞的异质性克隆性淋巴细胞增殖性疾病。
我们描述了一名患有独特原发性皮肤淋巴瘤的患者,其皮肤病变具有瘀伤样外观,中等大小至大的淋巴样肿瘤细胞具有CD4 +、CD43 +、CD56 +、CD2 -、CD3 -、CD8 -、T细胞受体阴性表型,且基因型未确定(T细胞受体β和免疫球蛋白重链处于种系构型,经聚合酶链反应结合变性梯度凝胶电泳分析后未检测到克隆性T细胞受体γ群体),放疗后快速复发。
这种非B、非T皮肤淋巴瘤无法用任何当前的淋巴瘤分类进行归类。它似乎代表了一种具有独特临床、组织学和分子特征的新疾病实体。