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J Clin Med. 2015 Jun 03;4(6):1229-39. doi: 10.3390/jcm4061229.

Cutaneous Squamous Cell Carcinomas in Organ Transplant Recipients.

Journal of clinical medicine

Ramya Chockalingam, Christopher Downing, Stephen K Tyring

Affiliations

  1. Medical School, the University of Texas Health Science Center at Houston, 6431 Fannin, Houston, TX 77030, USA. [email protected].
  2. Center for Clinical Studies, 1401 Binz, Suite 200, Houston, TX 77004, USA. [email protected].
  3. Center for Clinical Studies, 1401 Binz, Suite 200, Houston, TX 77004, USA. [email protected].
  4. Department of Dermatology, University of Texas Health Science Center at Houston, Houston, TX 77030, USA. [email protected].

PMID: 26239556 PMCID: PMC4484997 DOI: 10.3390/jcm4061229

Abstract

Non-melanoma skin cancers represent a major cause of morbidity after organ transplantation. Squamous cell carcinomas (SCC) are the most common cutaneous malignancies seen in this population, with a 65-100 fold greater incidence in organ transplant recipients compared to the general population. In recent years, human papillomaviruses (HPV) of the beta genus have been implicated in the pathogenesis of post-transplant SCCs. The underlying mechanism of carcinogenesis has been attributed to the E6 and E7 proteins of HPV. Specific immunosuppressive medications, such as the calcineurin inhibitors and azathioprine, are associated with a higher incidence of post-transplant SCCs compared to other immunosuppressive agents. Compared to other immunosuppressives, mTOR inhibitors and mycophenolate mofetil have been associated with a decreased risk of developing post-transplant non-melanoma skin cancers. As a result, they may represent ideal immunosuppressive medications in organ transplant recipients. Treatment options for post-transplant SCCs include surgical excision, Mohs micrographic surgery, systemic retinoid therapy, adjunct topical therapy, electrodessication and curettage, and radiation therapy. This review will discuss the epidemiology, risk factors, and management options of post-transplant SCCs. In addition, the underlying mechanisms of beta-HPV mediated carcinogenesis will be discussed.

Keywords: human papillomavirus (HPV); organ transplant; skin cancer; squamous cell carcinoma

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