2013
DOI: 10.1159/000350757
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Skin Cancer in Organ Transplant Recipients

Abstract: Organ transplant recipients (OTR) are at a significantly increased risk for developing a wide variety of skin cancers, particularly epithelial skin cancer, Merkel cell carcinoma and Kaposi's sarcoma. Melanoma, skin adnexal neoplasm and cutaneous lymphomas are also more common in OTR and may differ in their clinicopathologic presentation from tumors in immunocompetent patients. The accuracy of clinical diagnosis of suspected premalignant and malignant skin lesions in OTR is modest. Therefore, histopathological … Show more

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Cited by 60 publications
(36 citation statements)
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“…The majority of pediatric PTLD cases represent B‐cell lymphoproliferative disease with only 6% to 14% demonstrating the T‐cell phenotype . However, roughly 70% of primary cutaneous lymphoproliferative disease in the post‐transplant setting is of T‐cell origin . The overall 5‐year survival rate of PTLD in pediatric patients is better than in adults, reported to be between 60% and 70% …”
Section: Discussionmentioning
confidence: 99%
“…The majority of pediatric PTLD cases represent B‐cell lymphoproliferative disease with only 6% to 14% demonstrating the T‐cell phenotype . However, roughly 70% of primary cutaneous lymphoproliferative disease in the post‐transplant setting is of T‐cell origin . The overall 5‐year survival rate of PTLD in pediatric patients is better than in adults, reported to be between 60% and 70% …”
Section: Discussionmentioning
confidence: 99%
“…The incidence of MCC is generally higher in men than in women. Risk group includes the elderly people with immunosuppression from organ transplant and HIV infection [27,30]. MCC presents as a firm, painless, red-violet, rapidly enlarging, cutaneous nodule ( Figure 4) [25,27,31].…”
Section: Merkel Cell Carcinoma [Mcc]mentioning
confidence: 99%
“…Immunosuppression was identified as a risk factor for MCC following case reports for organ transplant recipients (Kempf et al, 2013) and HIV/AIDS patients (Engels et al, 2002). The subsequent discovery of MCPyV has led to a greater understanding of the pathogenesis of MCC, but the exact processes involved are yet to be determined, such as how the virus invades Merkel cells (Bhatia et al, 2011;Chang and Moore, 2012).…”
Section: Dr Youlden Et Almentioning
confidence: 99%