Abstract
The dysplastic nevus (DN) is a special kind of atypical melanocytic nevus with clinical and histologic features suggestive of an intermediate form between the common acquired melanocytic nevus and melanoma (1). Dysplastic nevi are important markers for both familial and nonfamilial melanoma. About 50% of patients with “sporadic” melanoma have been observed to have dysplastic nevi (2–5). Patients with dysplastic nevus syndrome (DNS) may also be at increased risk of conjunctival and intraocular melanoma (6). The incidence of DN in the general population has been estimated to be 1.8–7% (7–9) and possibly as high as 20% (10).
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Crutcher, W.A., Cohen, P.J. (1988). The Dysplastic Nevus Syndrome. In: Skin Cancer. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-3790-7_11
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DOI: https://doi.org/10.1007/978-1-4612-3790-7_11
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