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References 1. Elder DE, Goldman LI, Goldman SC, Greene MH, Clark WH Jr: The
dysplastic nevus syndrome: a phenotypic association of sporadic cutaneous
melanoma. Cancer 1980; 46: 1787-1794.
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The concept of "dysplastic nevus" has been proposed at the end of the 70's, as a particular nevus, identifiable clinically and histologically, playing the role of melanoma precursor and of risk marker [1]. Such a concept exploded in the scene of melanocytic lesions pathology, raising a large and hard controversy on several aspects of the problem. Although strongly contrasted, the concept of dysplastic nevus began to be accepted and used by many clinicians and pathologists. Examining the specific literature, however, it appears that authors, although they refer to the same concept, have deeply different opinions about primary aspects of the lesion (clinical and histological features, the precursor role, risk marker role)[2,3,4]. Particularly, at the beginning of 90's, it emerged that in dysplastic nevi clinical features do not constantly correspond to histological ones, showing that the lesion, as defined, can be hardly considered a true clinicopathological entity [5]. It also emerged that the histological border between dysplastic nevus and common nevus is not well defined, because many nevi showing intermediate characteristics do exist; under this light, it also appears hard that dysplastic nevus can be considered a real distinct histologic entity [6]. In fact, if nevi are investigated for the histological features considered to be specific of dysplastic nevi, rather than two distinct classes of lesions, they form a contiunuous spectrum of lesions showing an increasing incidence of atypical festures [7]. These results invite to reflect and seem to indicate, on one hand, that the concept of dysplastic nevus, as defined, cannot be used, and, in the other hand, that a new different approach to the nevi diagnosis is opportune. page 10
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page 13: Merkel cell carcinoma page 14: Basal cell carcinoma page 15: Melanoma in paediatric age |