Fernandez Kristen H, Rady Peter, Tyring Steven, Stone Mary S
Department of Dermatology, University of Iowa, Iowa City, IowaUniversity of Texas Medical School at Houston, Houston, Texas.
Pediatr Dermatol. 2014 May-Jun;31(3):400-2. doi: 10.1111/j.1525-1470.2012.01822.x. Epub 2012 Sep 3.
A 4-year-old girl with an established diagnosis of atopic dermatitis, previously severe and treated with cyclosporine, developed widespread papules that demonstrated changes consistent with epidermodysplasia verruciformis on biopsy. Human papilloma virus (HPV) typing was performed and was consistent with epidermodysplasia verruciformis-type HPV (type 5). These lesions rapidly resolved with a 2-week course of imiquimod. Rapid resolution and no family history of epidermodysplasia verruciformis make this most consistent with acquired epidermodysplasia verruciformis. This case is the first reported case of acquired epidermodysplasia verruciformis in a child without the human immunodeficiency virus and may be linked to cyclosporine use, which also has never been previously reported.
一名4岁女童,已确诊患有特应性皮炎,此前病情严重,曾用环孢素治疗,现出现广泛丘疹,活检显示病变与疣状表皮发育不良一致。进行了人乳头瘤病毒(HPV)分型,结果与疣状表皮发育不良型HPV(5型)相符。这些皮损在使用咪喹莫特治疗2周后迅速消退。迅速消退且无疣状表皮发育不良家族史,这最符合获得性疣状表皮发育不良。该病例是首例报道的无人类免疫缺陷病毒的儿童获得性疣状表皮发育不良病例,可能与环孢素的使用有关,此前也从未有过相关报道。