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http://dx.doi.org/10.23736/S2784-8671.23.07642-9DOI Listing

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Acquired epidermodysplasia verruciformis is a rare condition, secondary to a state of acquired immunosuppression and is characterized by a susceptibility to infection by human papillomavirus of the beta genus, which carries an increased risk of developing non-melanoma skin cancer. We report the case of a 39-year-old woman receiving a kidney transplant, treated with prednisone and tacrolimus, who after starting immunosuppressive therapy developed papules and warty plaques in the inguinal region. A skin biopsy was performed that was consistent with epidermodysplasia verruciformis, so it was decided to adjust immunosuppressive therapy to everolimus, which achieved a reduction in lesions.

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  • * A systematic review identified 80 relevant studies out of 126 searched, highlighting that the diagnosis of AEV can take an average of 7 years and lesions remain unchanged with standard HIV treatments, making management challenging.
  • * Current treatments for AEV, such as glycolic acid and imiquimod, show limited effectiveness, and while the risk of certain skin cancers is lower in A
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Article Synopsis
  • Most tumors result from genetic changes, but some are linked to viral infections like HPV, which can lead to specific skin conditions.
  • Epidermodysplasia verruciformis (EDV) is a rare HPV infection characterized by unique histological features and specific HPV subtypes.
  • The study discusses a particular type of EDV-related tumor found in two patients, highlighting consistent features and suggesting it could be a unique, reproducible form of skin tumor.
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