Manni E, Barachini P
Int J Immunopathol Pharmacol. 2009 Jul-Sep;22(3):841-4. doi: 10.1177/039463200902200331.
We describe the case of a 30-year-old female with no family history of psoriasis and suffering from Crohn's disease successfully treated with infliximab at the dosage of 5 mg/kg. On the 15th week from the start of therapy, the patient developed a palmoplantar pustular psoriasis, which spread to the arms, trunk and scalp with erythematosquamous plaques. Deeming the dermatitis onset due to the anti-TNF-alpha, we decided to discontinue infliximab, while starting with a topical therapy with emollients and corticosteroids and a systemic therapy with cyclosporine. These treatments achieved a clear improvement of psoriasis after 2 months and a complete regression of skin lesions after 4 months. Several cases have been reported of psoriasis induced by anti-TNF-alpha, which have shown to exert an effective therapeutic action on this disease. The pathogenic mechanism of such a paradoxical effect has not yet been explained, though a number of hypotheses were proposed, among which one of the most intriguing is that the rapid and strong blockade of TNF-alpha could result in an enhancement of INF-alpha activity with consequent induction of psoriasis.
我们描述了一名30岁女性的病例,她没有银屑病家族史,患有克罗恩病,以5mg/kg的剂量接受英夫利昔单抗治疗,治疗成功。在治疗开始后的第15周,患者出现掌跖脓疱型银屑病,其蔓延至手臂、躯干和头皮,伴有红斑鳞屑性斑块。考虑到皮疹发作是由抗TNF-α引起的,我们决定停用英夫利昔单抗,同时开始使用润肤剂和皮质类固醇进行局部治疗以及使用环孢素进行全身治疗。这些治疗在2个月后使银屑病明显改善,4个月后皮肤病变完全消退。已有多例抗TNF-α诱导的银屑病病例报道,这些病例已显示出对该疾病发挥有效的治疗作用。尽管提出了一些假设,但这种矛盾效应的致病机制尚未得到解释,其中最引人关注的一个假设是,TNF-α的快速和强烈阻断可能导致INF-α活性增强,从而引发银屑病。