Patel M J, Stockfleth E
Department of Dermatology, Skin Cancer Center Charité, University Hospital of Berlin, Berlin, Germany.
Br J Dermatol. 2007 May;156 Suppl 3:53-6. doi: 10.1111/j.1365-2133.2007.07859.x.
Progression from actinic keratosis (AK) and Bowen's disease (BD) to invasive disease involves a complex cascade of events. The preparation of diclofenac 3% gel (Solaraze; Shire Pharmaceuticals) has been shown to be efficacious and well tolerated in AK. The inhibition of the COX enzymes results in a decrease in downstream by-products of arachidonic acid metabolism. These metabolites have been shown to play a pivotal role in promoting epithelial tumour growth. Given its mechanism of action, we hypothosize that diclofenac 3% gel may have potential to halt the progression of actinic keratoses (AKs) in the setting of field cancerisation and BD. We report a series of five patients with BD, all treated with diclofenac 3% gel with clinical and histological clearance.
从光化性角化病(AK)和鲍恩病(BD)发展为浸润性疾病涉及一系列复杂的事件。已证明3%双氯芬酸凝胶(Solaraze;夏尔制药公司)制剂对AK有效且耐受性良好。COX酶的抑制导致花生四烯酸代谢的下游副产物减少。这些代谢产物已被证明在促进上皮肿瘤生长中起关键作用。鉴于其作用机制,我们推测3%双氯芬酸凝胶可能有潜力在皮肤原位癌和BD的背景下阻止光化性角化病(AK)的进展。我们报告了一系列五例BD患者,均接受3%双氯芬酸凝胶治疗,获得了临床和组织学清除。