Dendorfer Markus, Oppel Tilmann, Wollenberg Andreas, Prinz Jörg Christoph
Department of Dermatology and Allergology, Ludwig-Maximilians-University, Frauenlobstr. 9-11, D-80337 Munich, Germany.
Eur J Dermatol. 2003 Jan-Feb;13(1):80-2.
Keratoacanthoma (KA) is a rapidly growing tumour histologically resembling squamous cell carcinoma. Although it may regress spontaneously, KA is routinely treated by excision or radiation therapy. Here we report on the successful therapeutic use of imiquimod for the treatment of KA. Four patients with a one to six week history of facial KA were treated with imiquimod cream 5 % every second day for four to 12 weeks. In each patient, KA fully regressed under topical treatment with imiquimod. In three of the patients, KA had disappeared within four to six weeks. In two patients, disappearance was confirmed histologically. No recurrence occurred during a four- to six-month follow-up-period. Our observations indicate that topical immunostimulation with imiquimod may induce or promote immune defence mechanisms leading to KA regression. Imiquimod might therefore prove to be an effective non-invasive treatment modality for KA that warrants more extensive evaluation by clinical studies.
角化棘皮瘤(KA)是一种组织学上类似于鳞状细胞癌的快速生长肿瘤。尽管KA可能会自发消退,但通常通过手术切除或放射治疗。在此,我们报告咪喹莫特成功用于治疗KA。4例有1至6周面部KA病史的患者,每隔一天外用5%咪喹莫特乳膏,持续4至12周。每位患者的KA在咪喹莫特局部治疗下完全消退。其中3例患者的KA在4至6周内消失。2例患者经组织学证实病变消失。在4至6个月的随访期内未发生复发。我们的观察结果表明,咪喹莫特局部免疫刺激可能诱导或促进免疫防御机制,导致KA消退。因此,咪喹莫特可能是一种有效的KA非侵入性治疗方式,值得通过临床研究进行更广泛的评估。