Zafiriou Efterpi, Karampinis Emmanouil, Giannoulis George, Gravani Agoritsa, Gampeta Stella, Zachou Kalliopi
Department of Dermatology, Faculty of Medicine, School of Health Sciences, University General Hospital of Larissa, University of Thessaly, Larissa, GRC.
Department of Internal Medicine, Faculty of Medicine, School of Health Sciences, University General Hospital of Larissa, University of Thessaly, Larissa, GRC.
Cureus. 2024 Jul 13;16(7):e64474. doi: 10.7759/cureus.64474. eCollection 2024 Jul.
Generalized pustular psoriasis (GPP) presents as a severe variant of psoriasis featuring painful, sterile pustules on red skin and can lead to life-threatening complications if left untreated. The disease course is typically unpredictable, with periods of improvement, followed by relapses over extended periods. Managing GPP flares is challenging due to their potential to endanger the patient's life, underscoring the need for treatments that are both fast-acting and highly effective in the case of severe and systematically ill GPP patients. We present a case of a 48-year-old man with an extensive and severe GPP flare (GPP Physician Global Assessment score = 4), experiencing an extensive pustular rash on an erythematous base, intense skin exfoliation, and inflammation as well as systemic symptoms such as fever, hypotension, and general weakness. During the disease course, he developed comorbidities such as depression occurrence and an episode of an acute pulmonary embolism. Initial treatment attempts with acitretin and anakinra were not proved successful. Due to IL-36's significant role in GPP pathophysiology, the patient received treatment involving an IL-36 receptor antagonist (two infusions of 900 mg spesolimab administered one week apart), alongside continued acitretin therapy. This approach led to swift improvement, resolving pustules and skin inflammation and resulting in the patient's gradual recovery. This case highlights spesolimab's potential as a targeted therapy for severe GPP flares resistant to conventional treatments. However, further research is needed to establish its long-term safety and efficacy in managing GPP and related IL-36-mediated diseases.
泛发性脓疱型银屑病(GPP)是银屑病的一种严重变体,其特征为红色皮肤上出现疼痛的无菌脓疱,若不治疗可导致危及生命的并发症。该病病程通常不可预测,有病情改善期,随后会长期复发。由于GPP发作有可能危及患者生命,因此控制GPP发作具有挑战性,这凸显了对于重症和全身不适的GPP患者而言,需要快速起效且高效的治疗方法。我们报告一例48岁男性患者,其患有广泛且严重的GPP发作(GPP医师整体评估评分为4分),出现以红斑为基底的广泛脓疱疹、严重的皮肤脱屑和炎症以及发热、低血压和全身无力等全身症状。在病程中,他出现了诸如抑郁症发作和一次急性肺栓塞等合并症。最初使用阿维A和阿那白滞素的治疗尝试未获成功。由于白细胞介素-36(IL-36)在GPP病理生理学中起重要作用,该患者接受了包含IL-36受体拮抗剂的治疗(分两次输注900毫克司帕索利单抗,间隔一周),同时继续使用阿维A治疗。这种方法带来了迅速改善,脓疱和皮肤炎症消退,患者逐渐康复。该病例突出了司帕索利单抗作为针对常规治疗耐药的严重GPP发作的靶向治疗的潜力。然而,需要进一步研究以确定其在治疗GPP及相关IL-36介导疾病方面的长期安全性和有效性。