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淋巴瘤样丘疹病。病例报告为非典型细胞的单核细胞 - 巨噬细胞起源提供证据。

Lymphomatoid papulosis. Case report providing evidence for a monocyte-macrophage origin of the atypical cells.

作者信息

Poppema S, van Voorst Vader P C, Rozeboom-Uiterwijk T, Dijkstra J W

出版信息

Cancer. 1983 Oct 1;52(7):1178-82. doi: 10.1002/1097-0142(19831001)52:7<1178::aid-cncr2820520709>3.0.co;2-j.

Abstract

A patient with "classical" lymphomatoid papulosis is described in whom self-healing tumorous lesions occurred. Histologic, immunologic, enzyme histochemical and ultrastructural studies were performed. The atypical cells were found to be of monocyte-macrophage origin. The infiltrate also contained a variable number of suppressor-cytotoxic T-lymphocytes, depending on the stage of the tumorous lesions. The number of IgA positive B-lymphocytes in the peripheral blood was increased. The findings indicate that "classical" lymphomatoid papulosis is not a cutaneous T-cell lymphoma, but is the expression of an abnormal, immune reaction in the skin.

摘要

描述了一名患有“经典型”淋巴瘤样丘疹病的患者,其出现了自愈性肿瘤性病变。进行了组织学、免疫学、酶组织化学和超微结构研究。发现非典型细胞起源于单核细胞-巨噬细胞。根据肿瘤性病变的阶段,浸润物中还含有数量不等的抑制性-细胞毒性T淋巴细胞。外周血中IgA阳性B淋巴细胞数量增加。这些发现表明,“经典型”淋巴瘤样丘疹病不是皮肤T细胞淋巴瘤,而是皮肤异常免疫反应的表现。

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