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淋巴瘤样丘疹病。对一名有鳞屑性色素沉着性皮疹患者的组织学和免疫组织化学研究。

Lymphomatoid papulosis. Histologic and immunohistochemical studies in a patient with a scaly pigmented eruption.

作者信息

Tokura Y, Takigawa M, Oku T, Yamada M

出版信息

Arch Dermatol. 1986 Dec;122(12):1400-5. doi: 10.1001/archderm.122.12.1400.

Abstract

A patient with lymphomatoid papulosis type A showed a peculiar, scaly pigmented eruption on the broad skin areas as well as papulonodular lesions. Large atypical cells characteristic of the infiltrate of the disease were observed not only in the dermal infiltrate of papular lesions, but also in the perivascular infiltrate of the scaly pigmented lesions, indicating that the latter was one of the skin manifestations of lymphomatoid papulosis. Immunohistochemical studies showed that these atypical cells expressed Ki-1 and cellular activation-associated antigens such as HLA-DR, Tac, and T9, but were not reactive with T-cell specific antibodies Leu-1, Leu-3a, and Leu-2a.

摘要

一名A型淋巴瘤样丘疹病患者在广泛的皮肤区域出现了一种奇特的、有鳞屑的色素沉着性皮疹以及丘疹结节性损害。不仅在丘疹性损害的真皮浸润中观察到了该病浸润所特有的大的非典型细胞,在鳞屑性色素沉着性损害的血管周围浸润中也观察到了这些细胞,这表明后者是淋巴瘤样丘疹病的皮肤表现之一。免疫组织化学研究显示,这些非典型细胞表达Ki-1以及细胞活化相关抗原,如HLA-DR、Tac和T9,但与T细胞特异性抗体Leu-1、Leu-3a和Leu-2a无反应。

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