Abstract

Background and Objectives: Immunosuppressed individuals are at particularly increased risk for human papilloma virus-related infections. The primary objective of our study is to determine if there are any adverse effects associated with high-dose cimetidine treatment. A secondary objective is to report our experience with cimetidine in the treatment of cutaneous warts in pediatric heart transplant recipients. Methods and Results: This was a retrospective observational study. A total of 8 pediatric heart transplant recipients diagnosed with multiple recalcitrant warts were the subject of the study. All patients were treated with cimetidine (30–40 mg/kg/day) in two divided doses for 3 to 6 month durations. All patients had complete resolution of their lesions except 1 patient who had no clinical improvement. Of these 8 patients, one had recurrence of warts at one year follow-up, which resolved with restarting cimetidine therapy. One patient who had only 3 months of cimetidine therapy had immediate relapse after cimetidine was stopped. None of them had significant change in their tacrolimus trough, serum creatinine, and alanine transaminase levels. No adverse events were reported except one patient experienced mild gynecomastia. Conclusion: Cimetidine can be a safe and alternative treatment option for multiple warts in pediatric heart transplant recipients.

Highlights

  • Cutaneous warts are caused by human papilloma virus (HPV), a double-strandedDNA papovavirus, which commonly affect children and adolescents and can be functionally and cosmetically disabling

  • DNA extraction from cutaneous warts showed that warts in solid organ transplant patients carried similar HPV types as the general population [4]

  • We reviewed the tacrolimus drug levels, renal and liver function results pre- and post-cimetidine therapy

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Summary

Introduction

Cutaneous warts (verrucae) are caused by human papilloma virus (HPV), a double-strandedDNA papovavirus, which commonly affect children and adolescents and can be functionally and cosmetically disabling. HPV 27, 57, 2, and 1 are the most prevalent HPV types in cutaneous warts in general population [1]. The prevalence for warts is 24.4% in 217 consecutive pediatric solid-organ transplant patients [3]. DNA extraction from cutaneous warts showed that warts in solid organ transplant patients carried similar HPV types as the general population [4]. A secondary objective is to report our experience with cimetidine in the treatment of cutaneous warts in pediatric heart transplant recipients. All patients had complete resolution of their lesions except 1 patient who had no clinical improvement Of these 8 patients, one had recurrence of warts at one year follow-up, which resolved with restarting cimetidine therapy. Conclusion: Cimetidine can be a safe and alternative treatment option for multiple warts in pediatric heart transplant recipients

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