Acquired epidermodysplasia verruciformis in a renal transplant recipient - Case report

• Main Authors: Alena Darwich Mendes (Author), Maraya de Jesus Semblano Bittencourt (Author), Emanuella Rosyane Duarte Moure (Author), Camila Maria D'Macedo (Author), Igor Nagai Yamaki (Author), Dyandra Moreira de Araujo (Author)
• Format: Book
• Published: Sociedade Brasileira de Dermatologia, 2014-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 0365-0596; 10.1590/abd1806-4841.20142803
• Keywords: Epidermodysplasia verruciformis; Immunosuppression; Kidney transplantation; Dermatology; RL1-803
• Source: Anais Brasileiros de Dermatologia, Vol 89, Iss 1, Pp 144-146 (2014)

A 24-year-old male patient, who underwent kidney transplant six years ago due to Lupus nephritis, for the last two years presented asymptomatic erythematous scaly plaques on the abdomen and areas exposed to light. Post-transplantation immunosuppressive medications included prednisone, mycophenolate sodium and sirolimus. The histopathologic features were typical for epidermodysplasia verruciformis. Epidermodysplasia verruciformis is a rare autosomal recessive genodermatosis with increased susceptibility to specific strains of cutaneous human papilloma virus. The term ''acquired epidermodysplasia verruciformis'' was recently introduced to the literature and describes epidermodysplasia verruciformis occurring in patients with impaired cell-mediated immunity. We report an additional case associated to immunosuppression after kidney transplantation.