All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a healthcare professional.
Introducing
Now you can personalise
your PsOPsA Hub experience!
Bookmark content to read later
Select your specific areas of interest
View content recommended for you
Find out moreThe PsOPsA Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the PsOPsA Hub cannot guarantee the accuracy of translated content. The PsOPsA Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The PsOPsA Hub is supported by educational grants. All educational content is developed independently by SES in collaboration with our expert steering committee, with no input or influence from financial supporters. We would like to express our gratitude to the following companies for their support: • UCB: For website development, launch, and ongoing maintenance. • UCB: For educational content and news updates.
GPP is a rare, severe type of psoriasis that can cause recurrent erythema, pustules, and systemic inflammation. Li et al. published the case of a 52-year-old female with recurrent GPP for 2 years in Anais Brasileiros de Dermatologia. Symptoms included widespread erythema, sterile pustules, pain, generalized fatigue, and limb swelling. After discontinuing oral medications, symptoms were exacerbated. Previous treatments included oral acitretin, prednisone, and ixekizumab for 12 weeks, which proved ineffective. The IL-36 receptor inhibitor spesolimab was administered, with outcomes summarized here. |
Key learnings |
On admission, findings included diffuse erythema, numerous pustules, tenderness, elevated skin temperature, severe disease scores (GPPGA: 11; GPPASI: 38.3), and laboratory abnormalities (elevated WBC count, neutrophils, CRP, and decreased albumin). Skin biopsy confirmed a diagnosis of GPP. |
Spesolimab was administered as a single 900 mg IV dose over 90 minutes after pre-biologic screening. Within 24 hours, pustules cleared almost entirely, and erythema began resolving (GPPGA: 5; GPPASI: 11.7). |
After 5 days, minimal desquamation and no new lesions were observed (GPPGA: 2; GPPASI: 5) and laboratory values normalized. The patient maintained remission with topical corticosteroids at 3-month follow-up. |
In this case study, spesolimab effectively managed acute GPP when conventional treatments failed. This highlights the role of the IL-36 pathway in GPP pathogenesis and suggests that spesolimab can be an effective option for refractory cases. |
Abbreviations: CRP, C-reactive protein; GPP, generalized pustular psoriasis; GPPASI, Generalized Pustular Psoriasis Area and Severity Index; GPPGA, Generalized Pustular Psoriasis Physician Global Assessment; IL, interleukin; IV, intravenous; WBC, white blood cell.
Subscribe to get the best content related to Psoriasis and Psoriatic Arthritis delivered to your inbox