Living with GPP - Make the most out of your doctor's appointments
Understanding GPP
If you or someone you know has been diagnosed with Generalised Pustular Psoriasis (GPP), it’s important to know what GPP is.
GPP is a rare type of psoriasis.1 It is a lifelong, persistent autoinflammatory disease which unfortunately may be life-threatening.2 If left untreated, it can lead to complications including sepsis (infection), kidney failure, heart failure and acute respiratory distress syndrome (fluid in the lungs).3
Supporting your GPP diagnosis
GPP flares include the eruption of pustules that can appear suddenly and cover large areas of the skin.4 Pustules are inflamed, blister-like sores (lesions) that are filled with pus that appear on the skin’s surface, which can be scaly, flaky or itchy and can also be painful.10,11 You may experience (systemic) symptoms such as fever, joint pain, and muscle weakness.
Living with GPP
There is more than you see
When living with GPP, recognising what triggers your flares is a big part of managing your disease.
GPP Community
Hear from people living with GPP
Psychological support
Caregiver support
Centres of Excellence
Did you know that Centres of Excellence can support with your diagnosis and disease
management?
More information
Understanding GPP and all its aspects can help with your overall disease journey. Download our informational materials and learn more about this rare disease and how it can be managed.
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- Strober B, et al. Unmet medical needs in the treatment and management of generalized pustular psoriasis flares: evidence from a survey of Corrona registry dermatologists. Dermatol Ther (Heidelb). 2021;11(2):529-541. doi:10.1007/s13555-021-00493-0
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- Global Commission to End the Diagnostic Odyssey for Children with a Rare Disease [Internet]. Global Commission. 2022 [cited 4 March 2022]. Available from: https://www.globalrarediseasecommission.com/report
- Strober B, Leman J, Mockenhaupt M, Nakano de Melo J, Nassar A, Prajapati VH, Romanelli P, Seneschal J, Tsianakas A, Wei LY, Yasuda M, Yu N, Hernandez Daly AC, Okubo Y. Unmet Educational Needs and Clinical Practice Gaps in the Management of Generalized Pustular Psoriasis: Global Perspectives from the Front Line. Dermatol Ther (Heidelb). 2022;12(2):381-393. doi: 10.1007/s13555-021-00661-2
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- Sampogna F, et al. IDI Multipurpose Psoriasis Research on Vital Experiences (IMPROVE) investigators. Measuring quality of life of patients with different clinical types of psoriasis using the SF-36. Br J Dermatol. 2006;154(5):844-9. doi: 10.1111/j
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- Johnston A, et al. IL-1 and IL-36 are dominant cytokines in generalized pustular psoriasis. J Allergy Clin Immunol. 2017;140(1):109-120. doi: 10.1016/j.jaci.2016.08.056
- Robinson A, et al. Treatment of pustular psoriasis: From the Medical Board of the National Psoriasis Foundation. Journal of the American Academy of Dermatology. 2012;67(2):279-288. doi: 10.1016/j.jaad.2011.01.032
- Liang Y, et al. Psoriasis: a mixed autoimmune and autoinflammatory disease. Curr Opin Immunol. 2017;49:1-8. doi:10.1016/j.coi.2017.07.007
- Benjegerdes K, et al. Pustular psoriasis: pathophysiology and current treatment perspectives. Psoriasis: Targets and Therapy. 2016;6:131-144. doi: 10.2147/PTT.S98954
- Choon SE, et al. Clinical Course and Characteristics of Generalized Pustular Psoriasis. Am J Clin Dermatol. 2022;23(Suppl 1):21-29. doi: 10.1007/s40257-021-00654-z
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- Pustular Psoriasis [Internet]. eMedicineHealth. 2022 [cited 4 March 2022]. Available from: https://www.emedicinehealth.com/pustular_psoriasis/article_em.htm
- ClinicalTrials.gov. [Internet] A 5-year Study to Test BI 655130 in Patients With Generalized Pustular Psoriasis Who Took Part in Previous Studies With BI 655130 - Full Text View - Clinicaltrials.gov. 2022 [cited 5 April 2022]. Available from: https://www.clinicaltrials.gov/ct2/show/NCT03886246?cond=Generalised+Pustular+Psoriasis&draw=2&rank=5
- Sampogna F, et al. Measuring quality of life of patients with different clinical types of psoriasis using the SF-36. British Journal of Dermatology. 2006;154(5):844-849. doi: 10.1111/j.1365-2133.2005.07071.x
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