Chun S I, Lee J S, Kim N S, Park K D
CHA General Hospital, Department of Dermatology, Yonsei University College of Medicine, Seoul, Korea.
J Dermatol. 1995 Sep;22(9):690-2. doi: 10.1111/j.1346-8138.1995.tb03900.x.
A 40-year-old man who had received long term immunosuppressive treatment for 14 years following kidney transplantation developed multiple skin lesions on both antecubital fossae, scalp, and both lower extremities. Histopathologic findings from three skin regions revealed characteristic features of epidermolytic hyperkeratosis, verruca vulgaris, and disseminated superficial porokeratosis, respectively. Although immunocompromised individuals may demonstrate verruca vulgaris or porokeratosis, disseminated epidermolytic acanthoma (DEA) has not been reported to be associated with immunosuppressed status. We suggest that immunosuppression may play a role in the pathogenesis of DEA, as shown in our case.
一名40岁男性在肾移植后接受了14年的长期免疫抑制治疗,双侧肘窝、头皮和双下肢出现多处皮肤病变。来自三个皮肤区域的组织病理学检查结果分别显示为表皮松解性角化过度、寻常疣和播散性浅表性光化性角化病的特征性表现。虽然免疫功能低下的个体可能会出现寻常疣或光化性角化病,但播散性表皮松解性棘皮瘤(DEA)尚未被报道与免疫抑制状态有关。如我们的病例所示,我们认为免疫抑制可能在DEA的发病机制中起作用。