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伴有库欣综合征的泛发性脓疱型银屑病:司库奇尤单抗治疗有效的病例

Generalized Pustular Psoriasis with Cushing's Syndrome: A Case of Effective Spesolimab Treatment.

作者信息

Peng Guoyao, Zhang Yun, Zhang Shuang, Li You, Luo Liping, Luo Jiaxin, Nie Xinyi, Zhang Hongwei, Liao Chengcheng

机构信息

Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan Province, People's Republic of China.

出版信息

Biologics. 2025 May 10;19:321-329. doi: 10.2147/BTT.S521363. eCollection 2025.

Abstract

Generalized pustular psoriasis (GPP) is a rare neutrophilic skin disease characterized by persistent symptoms and sudden onset of painful, sterile pustules. These pustules may be accompanied by systemic inflammation and can be life-threatening in severe cases. Presently, there is an absence of standardized guidelines for treatment, and the majority of conventional treatments employed by clinicians are predicated on the utilization of glucocorticosteroids, immunosuppressants, and retinoids to attain anti-inflammatory and immune-suppressing effects. However, the therapeutic effect is often unsatisfactory and patients are prone to side effects. The IL-36 receptor monoclonal antibody, Spesolimab, signifies a novel therapeutic modality that has received approval from both the National Drug Administration (NMPA) of China and the US Food and Drug Administration (FDA) for the management of acute exacerbations of GPP. We report a case of a 40-year-old male patient diagnosed with GPP who had no significant improvement in symptoms and development of Cushing's syndrome after up to six months of treatment with glucocorticoids, immunosuppressants, and retinoids. The patient was treated with Spesolimab, a monoclonal antibody, resulting in a substantial improvement in symptoms. This development offers novel treatment options and provides a reference for clinical medication for patients with this particular type of GPP.

摘要

泛发性脓疱型银屑病(GPP)是一种罕见的嗜中性皮肤病,其特征为症状持续且突然出现疼痛的无菌脓疱。这些脓疱可能伴有全身炎症,严重时可危及生命。目前,缺乏标准化的治疗指南,临床医生采用的大多数传统治疗方法基于使用糖皮质激素、免疫抑制剂和维甲酸来达到抗炎和免疫抑制效果。然而,治疗效果往往不尽人意,患者容易出现副作用。白细胞介素-36受体单克隆抗体司库奇尤单抗(Spesolimab)代表了一种新型治疗方式,已获得中国国家药品监督管理局(NMPA)和美国食品药品监督管理局(FDA)批准用于治疗GPP急性加重期。我们报告一例40岁男性患者,诊断为GPP,在接受糖皮质激素、免疫抑制剂和维甲酸治疗长达六个月后症状无明显改善且出现库欣综合征。该患者接受单克隆抗体司库奇尤单抗治疗后症状大幅改善。这一进展提供了新的治疗选择,并为这类GPP患者的临床用药提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccde/12077406/fd70f357dcc0/BTT-19-321-g0001.jpg

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