Harder D, Kuhn A, Mahrle G
Universitäts-Hautklinik Köln.
Z Hautkr. 1989 Jul 15;64(7):593-5.
A 54-year-old female patient recurrently developed disseminated papules, red-brown in color and partly ulcerous, which spontaneously disappeared after 3-6 weeks. Histological examination revealed dense infiltration of atypical lymphocytes with epidermotropism. Immunohistological analysis showed predominantly helper T-cells (CD 4). Accordingly, we established the diagnosis of lymphomatoid papulosis. There was no evidence of malignant lymphoma.
一名54岁女性患者反复出现播散性丘疹，呈红棕色，部分有溃疡，3 - 6周后自行消失。组织学检查显示非典型淋巴细胞呈致密浸润并向表皮浸润。免疫组织学分析显示主要为辅助性T细胞（CD4）。据此，我们诊断为淋巴瘤样丘疹病。无恶性淋巴瘤的证据。
