蕈样真菌病
真皮
病理
紫癜(腹足类)
医学
真皮乳头状
表皮(动物学)
皮肤病科
CD8型
生物
淋巴瘤
免疫学
解剖
免疫系统
生态学
作者
Tsukasa Ugajin,Takahiro Satoh,Hiroo Yokozeki,Kiyoshi Nishioka
出处
期刊:PubMed
[National Institutes of Health]
日期:2005-11-11
卷期号:15 (6): 489-91
被引量:22
摘要
A case of pigmented purpuric eruptions evolving to mycosis fungoides during the 4-year follow-up period is described. Clinical manifestation was characterized by petechial lesions with irregular shaped, diffusely pigmented plaques partly sharing morphological similarities with chronic pigmented purpura. Histologically, lymphocytes infiltrated around the capillaries of the superficial dermis with extravasated erythrocytes as well as into the epidermis to form Pautrier microabscesses. Whereas CD4+ cells were observed in the epidermis and upper dermis, CD8+ cells tended to be distributed around the capillaries. Notably, the Rumpel-Leede test revealed extensive punctuate purpura limited to the lesional skin. The aggregation response of platelets was not impaired. Either CD4+ tumor lymphocytes or CD8+ reactive lymphocytes appeared to induce capillary damage resulting in the formation of petechial lesions. Pigmented purpuric eruptions, such as atypical chronic pigmented purpura, is thus an important initial clinical manifestation of mycosis fungoides.
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