Yu Keyi, Bao Huaye, Wu Xingang
Department of Dermatology, Hangzhou Third Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, Zhejiang, People's Republic of China.
Department of Dermatology, Hangzhou Third People's Hospital, Hangzhou, Zhejiang, People's Republic of China.
Clin Cosmet Investig Dermatol. 2025 Jan 16;18:105-108. doi: 10.2147/CCID.S493665. eCollection 2025.
Generalized Pustular Psoriasis (GPP) is a rare, severe, life-threatening form of psoriasis and often resistant to conventional systemic therapy. It can be induced by deficiency of interleukin (IL)-36 receptor antagonist. Treatment of patients with GPP is often difficult, and there is no consensus on the best options available to date. However, multiple biologics approved for use in plaque-type psoriasis have also been used in GPP. Here, we report a 6-year-old boy with GPP who was misdiagnosed with AGEP and was treated with corticosteroids but did not respond well. He showed significant improvement following secukinumab treatment. Our case report indicates that IL-17A inhibition as a promising therapeutic option for pediatric GPP without combination with other systemic agents.
泛发性脓疱型银屑病(GPP)是一种罕见、严重且危及生命的银屑病类型,通常对传统的全身治疗耐药。它可由白细胞介素(IL)-36受体拮抗剂缺乏引起。GPP患者的治疗往往很困难,目前对于最佳治疗方案尚无共识。然而,多种已获批用于斑块型银屑病的生物制剂也被用于GPP治疗。在此,我们报告一名6岁的GPP男孩,他曾被误诊为急性泛发性发疹性脓疱病(AGEP)并接受了皮质类固醇治疗,但效果不佳。他在接受司库奇尤单抗治疗后有显著改善。我们的病例报告表明,抑制IL-17A作为儿科GPP的一种有前景的治疗选择,无需联合其他全身用药。