Smolle J, Kaudewitz P, Aberer E, Torne R, Burg G, Kerl H
Universitätsklinik für Dermatologie und Venerologie Graz.
Hautarzt. 1987 Aug;38(8):461-6.
We investigated 46 cases of cutaneous lymphoma and pseudolymphoma by immunohistochemical methods using a panel of monoclonal antibodies. Of the cutaneous T cell lymphomas, 2 did not show the classic helper phenotype but revealed a predominance of suppressor cells in one case and of immature thymocytes in the other. Cutaneous B cell lymphomas of low-grade malignancy were characterized by the presence of completely developed T zones between the B cell areas. B cell lymphomas of high-grade malignancy revealed an immunohistologically homogeneous infiltrate. Cutaneous pseudolymphomas can be classified in T cell pseudolymphomas (lymphocytic infiltration, lymphomatoid papulosis) and B cell pseudolymphomas. Lymphadenosis cutis benigna with germinal center cell differentiation was clearly distinguishable from other B cell pseudolymphomas, which are considered to comprise mainly peripheral B lymphocytes. Immunohistological methods are obviously useful in the classification of lymphoproliferative diseases of the skin and can make a contribution to increasing our understanding of them.
我们使用一组单克隆抗体,通过免疫组织化学方法对46例皮肤淋巴瘤和假性淋巴瘤进行了研究。在皮肤T细胞淋巴瘤中,有2例未表现出典型的辅助细胞表型,其中1例显示抑制细胞占优势,另一例显示未成熟胸腺细胞占优势。低级别恶性皮肤B细胞淋巴瘤的特征是在B细胞区域之间存在完全发育的T区。高级别恶性B细胞淋巴瘤显示免疫组织学上均匀的浸润。皮肤假性淋巴瘤可分为T细胞假性淋巴瘤(淋巴细胞浸润、淋巴瘤样丘疹病)和B细胞假性淋巴瘤。具有生发中心细胞分化的皮肤良性淋巴腺病与其他B细胞假性淋巴瘤明显不同,后者主要被认为由外周B淋巴细胞组成。免疫组织学方法显然有助于皮肤淋巴增殖性疾病的分类,并有助于增进我们对它们的理解。