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Published on: December 15, 2011
Paradoxic eczema in infants after heart transplantation
Stephanie R Jackson Cullison1, Elaine C Siegfried2
1Department of Dermatology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Insights
New-onset eczema, analogous to psoriasis, can occur in children after cardiac transplants treated with systemic tacrolimus. Reducing tacrolimus dosage may improve skin conditions.
Area of Science:
- Dermatology
- Immunology
- Transplantation
Background:
- Tumor necrosis factor inhibitors are known to cause new-onset psoriasis.
- Systemic tacrolimus is a calcineurin inhibitor used for immunosuppression post-transplant and topically for eczema.
Observation:
- Three pediatric cardiac transplant recipients developed a paradoxical eczema.
- Eczema onset occurred 2-48 months after initiating systemic tacrolimus therapy.
Findings:
- The observed eczema is analogous to drug-induced psoriasis seen with other immunosuppressants.
- Anecdotal evidence suggests that tapering tacrolimus and switching to alternative immunosuppressants may resolve the skin condition.
Implications:
- This paradoxical eczema highlights a potential adverse effect of systemic tacrolimus in transplant patients.
- Management strategies should focus on optimizing skin barrier, minimizing triggers, and careful selection of immunosuppressive regimens.
- Further research is needed to understand the mechanism and refine treatment protocols for tacrolimus-induced eczema.
Abstract:
New-onset psoriasis in patients receiving tumor necrosis factor inhibitors is well recognized in children and adults. We describe three children who underwent cardiac transplantation and developed an analogous form of paradoxic eczema occurring 2-48 months after starting systemic tacrolimus, a drug widely used topically to treat eczema. Anecdotal reports and our experience suggest that tacrolimus taper with alternative systemic antirejection immunosuppressant may lead to skin clearance. Pending additional insight, treatment should include optimizing skin barrier function, minimizing microbial and allergic triggers, and coordinating care to choose the best-tolerated systemic immunosuppressant regimen at the lowest effective dose.
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