## BACKGROUND. The frequency of in situ melanoma is increasing, and it is often diagnosed fortuitously by histology. ## METHODS. We retrospectively reviewed 121 melanomas in situ in 113 patients with the aim of identifylng the clinical features of, and optimal surgical treatment for this cutaneou
Cancer risk in patients with earlier diagnosis of cutaneous melanoma In situ
✍ Scribed by Cecilia Wassberg; Magnus Thörn; Jonathan Yuen; Timo Hakulinen; Ulrik Ringborg
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- French
- Weight
- 92 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
We calculated the short-term and long-term risks of developing cancer among 3,766 patients with a diagnosis of cutaneous melanoma in situ in Sweden from 1958 to 1992. In total, 393 patients developed a primary cancer at any site compared with an expected number of 177 [standardized incidence ratio (SIR) ؍ 2.2, 95% confidence interval (CI) ؍ 2.0-2.4]. Patients below 60 years of age at diagnosis had the highest SIR (2.7, 95% CI ؍ 2.3-3.2). The overall risks were similar between men and women. The highest risk was seen during the first year of follow-up, though the risk remained elevated also after 15 or more years of follow-up. For specific sites, the highest SIR was found for developing invasive cutaneous malignant melanoma (SIR ؍ 22.2). The risk of subsequent primary non-melanoma skin cancer was elevated 8-fold in men and almost 7-fold in women. An elevated risk was also found for female breast cancer (SIR ؍ 1.4). Especially among women, other sites with increased cancer risk (though not significant) were non-Hodgkin's lymphoma (SIR ؍ 1.9), multiple myeloma (3.2) and cancers of the colon (1.6) and pancreas (1.6). In conclusion, patients with melanoma in situ run a generally increased risk of developing primary cancers, especially cutaneous malignant melanoma and non-melanoma skin cancer. The increased long-term risk of cancer after diagnosis of melanoma in situ may be due to continuing carcinogenic exposure or to intrinsic tumor susceptibility. Int.
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