Millak Laura, Hahn Matthias, Fischer Judith, Volc Sebastian
Department of Dermatology, University Hospital Tuebingen, Tuebingen, Germany.
Institute of Human Genetics, Medical Center, University of Freiburg, Freiburg, Germany.
Front Med (Lausanne). 2025 Jul 22;12:1637045. doi: 10.3389/fmed.2025.1637045. eCollection 2025.
Pityriasis rubra pilaris is a rare inflammatory papulosquamous skin disease without any approved treatment options. Variants in the (caspase recruitment domain family member 14) gene have been identified to play a role in the pathophysiology of atypical juvenile PRP by activating the IL-23/IL-17A cytokine axis, highlighting this pathway as a potential target of therapy. Here, we present a case of successful treatment with ixekizumab, a humanized monoclonal anti-IL-17A antibody, in an atypical juvenile PRP (type V) patient with a novel variant of mutation.
红皮病型毛发红糠疹是一种罕见的炎症性丘疹鳞屑性皮肤病,目前尚无任何获批的治疗方案。已确定(半胱天冬酶募集结构域家族成员14)基因的变异通过激活IL-23/IL-17A细胞因子轴在非典型青少年毛发红糠疹的病理生理学中发挥作用,这突出表明该途径是一个潜在的治疗靶点。在此,我们报告一例非典型青少年毛发红糠疹(V型)患者,其携带一种新的 突变,使用人源化抗IL-17A单克隆抗体司库奇尤单抗治疗成功的病例。