Clinical risk factors associated with nonmelanoma skin cancer in renal transplant recipients

被引:172
|
作者
Ramsay, HM
Fryer, AA
Reece, S
Smith, AG
Harden, PN
机构
[1] Keele Univ, N Staffordshire Hosp, Directorate Renal Med, Dept Dermatol, Stoke On Trent, Staffs, England
[2] Keele Univ, N Staffordshire Hosp, Dept Renal Med, Stoke On Trent, Staffs, England
[3] Keele Univ, N Staffordshire Hosp, Ctr Cell & Mol Med, Postgrad Med Sch, Stoke On Trent, Staffs, England
关键词
renal transplantation; skin cancer; kidney graft; immunosuppression;
D O I
10.1053/ajkd.2000.8290
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
A single-center, cross-sectional, longitudinal study was conducted to determine the prevalence, annual incidence, and clinical risk factors for skin cancer in a white renal transplant population. One hundred eighty-two white patients (95% of population) with functioning allografts, a mean age at transplantation of 38.9 +/- 15.6 (SD) years, and a mean follow-up of 8.5 +/- 6.3 years were interviewed and examined between May 1997 and June 1999. All case notes were carefully reviewed. Since transplantation, 16.5% of the patients had developed nonmelanoma skin cancer; 15.4%, actinic keratoses (AK); 53%, viral warts; and 1.6%, lentigo maligna melanoma (n = 3). Thirty-nine percent of the tumors were detected as a consequence of this study and 20% of these occurred on covered body sites. The squamous cell (SCC)-basal cell carcinoma (BCC) ratio was 3.8:1, Eighty-two percent of the patients were examined a second time 12 months after the initial assessment. Using these data to identify new lesions, the annual incidence was calculated at 6.5%, increasing to 10.5% at more than 10 years posttransplantation. Duration of Immunosuppression, older age at transplantation, presence of AK, male sex, and outdoor occupation were significantly associated with both SCC and BCC; SCC alone was associated with a history of having smoked tobacco. Early identification of those at greatest risk using a clinical risk profile may allow the development of more structured preventative and surveillance strategies than currently exist. (C) 2000 by the National Kidney Foundation, Inc.
引用
收藏
页码:167 / 176
页数:10
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