Kwon O S, Cho K H, Song K Y
Department of Dermatology, Seoul National University, College of Medicine, Korea.
J Dermatol. 1997 Jan;24(1):54-6. doi: 10.1111/j.1346-8138.1997.tb02740.x.
A 23-year-old man with Langerhans cell histiocytosis presented with asymptomatic, purplish, slightly scaly, confluent papules of one year's duration. Histological studies of biopsy specimens revealed a dense infiltrate of histiocytic mononuclear cells beneath the epidermis; these cells reacted strongly with anti-S-100 antibodies. Extensive investigations failed to detect systemic involvement. He was treated with repeated oral 8-methoxypsoralen (8-MOP) plus ultraviolet A (PUVA) therapy three times a week for two months and then once or twice with maintenance phototherapy. The lesions did not recur during the four-month follow-up period.
一名患有朗格汉斯细胞组织细胞增多症的23岁男性,出现无症状的紫色、轻度鳞屑性、融合性丘疹,病程1年。活检标本的组织学研究显示,表皮下有密集的组织细胞单核细胞浸润;这些细胞与抗S-100抗体强烈反应。广泛检查未发现系统性受累。他接受了每周3次、持续2个月的重复口服8-甲氧基补骨脂素(8-MOP)加紫外线A(PUVA)治疗,然后进行了1至2次维持光疗。在4个月的随访期内,病变未复发。