Paradoxical psoriasis in pediatric patients: A systematic review
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Updated: Oct 23, 2025

The Goeckerman Regimen for the Treatment of Moderate to Severe Psoriasis
Published on: July 11, 2013
Benoit M Cyrenne1, Alyssa S Parpia2, Cathryn Sibbald1,3
1Division of Dermatology, Department of Medicine, University of Toronto, Toronto, ON, Canada.
Insights
Paradoxical psoriasis is a common side effect in children treated with TNF-α inhibitors. Most cases can be managed with continued therapy and topical treatments, but switching to another TNF-α inhibitor is often ineffective.
Area of Science:
- Dermatology
- Pediatric Rheumatology
- Immunology
Background:
- Paradoxical psoriasis is an emerging adverse effect in pediatric patients treated with biologic agents.
- The clinical presentation and management of these cases are not well-established.
Purpose of the Study:
- To determine the incidence, clinical characteristics, and treatment outcomes of psoriasis induced by TNF-α inhibitors in pediatric patients.
Main Methods:
- A systematic review of published literature, including case reports and cohort studies, focusing on paradoxical psoriasis linked to TNF-α inhibitor use.
Main Results:
- 4.6% of pediatric patients (210/4564) treated with TNF-α inhibitors developed paradoxical psoriasis.
- Infliximab (8.3%) and adalimumab (3.3%) were most frequently implicated.
- Scalp and ear involvement were common; 63.3% continued TNF-α inhibitor therapy.
- Switching to a non-TNF-α inhibitor resulted in 81% clearance, while switching to another TNF-α inhibitor yielded only 32% clearance.
Conclusions:
- TNF-α inhibitor-induced psoriasis is a notable adverse event in pediatric populations.
- Management often involves continuing the original TNF-α inhibitor with adjunctive topical or systemic therapies.
- Discontinuation of TNF-α inhibitors necessitates careful consideration, as switching to a different agent in the same class is less effective for resolution.
Background:
Paradoxical psoriasis occurs in pediatric patients following treatment with biologic agents. These presentations are not well described, and optimal treatment strategies have not been established.
Objective:
To describe the reported rates, demographic characteristics, clinical presentation, and treatment options for TNF-α inhibitor-induced psoriasis.
Methods:
Systematic review of published cases and cohort studies of paradoxical psoriasis induced by biologic agents, with specific reference to TNF-α inhibitors.
Results:
We identified 4564 pediatric patients treated with TNF-α inhibitors, of whom 210 (4.6%) developed paradoxical psoriasis. Infliximab was the drug most likely to induce psoriasis (8.3%), followed by adalimumab (3.3%). Individual-level data were acquired from 129 individuals with a mean age of 13.6 years (SD: 4.0); 45.0% were male. The scalp was the most commonly affected area (47.5%), followed by the ears (30.8%). Most (63.3%) patients were continued on TNF-α inhibitor therapy. Among those who switched TNF-α inhibitors, only 32.0% had complete clearance of their skin lesions. Among patients who were switched to a non-TNF-α inhibitor, 81% had complete clearance of their paradoxical psoriasis.
Limitations:
Data were acquired from retrospective studies including case reports and case series.
Conclusion:
TNF-α inhibitor-induced psoriasis is a common adverse effect; however, most patients can continue their original therapy and be managed with skin-directed topical or systemic medications. If a patient requires medication discontinuation, switching to a new TNF-α inhibitor is unlikely to lead to resolution of their skin lesions.
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