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      Stardust Pattern as Evolution of Pigmented Spitz Nevi During Childhood

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          Abstract

          Introduction

          Spitz nevi (SN) are benign melanocytic proliferations frequently occurring in children. Some pigmented SN with a starburst pattern evolve into the “stardust” one, which is characterized by a central, black to gray, hyperpigmented area and remnants of a brown network at the periphery. These dermoscopy changes are often the first alert to induce excision.

          Objectives

          The aim of this study is to enlarge the case series of stardust SN in children, in order to increase confidence with this new dermoscopic pattern and reduce unnecessary excisions.

          Methods

          This retrospective observational study was conducted with SN cases received from IDS members. The inclusion criteria were: clinical and/or histopathologic diagnosis of Spitz naevus with starburst appearance in children <12 years old, availability of a dermoscopic image at baseline and after follow-up of at least 1 year, availability of patient data. The dermoscopic images and their changes over time were assessed by three evaluators in consensus.

          Results

          38 SN were enrolled, with a median age of 7 years and a median FUP duration of 15,5 months. Comparing the evolution with time of FUP, no significant differences were found between growing and involuting lesions in terms of patient age and sex, location and palpability of lesions.

          Conclusions

          The long follow-up reported in our study could really support the concept of benignity of changing SN. A conservative approach is acceptable for nevi showing the stardust pattern, because it may be considered a physiological evolution of pigmented Spitz nevus, and urgent surgeries could be avoided.

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          Most cited references13

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          Genetics of melanocytic nevi.

          Melanocytic nevi are a benign clonal proliferation of cells expressing the melanocytic phenotype, with heterogeneous clinical and molecular characteristics. In this review, we discuss the genetics of nevi by salient nevi subtypes: congenital melanocytic nevi, acquired melanocytic nevi, blue nevi, and Spitz nevi. While the molecular etiology of nevi has been less thoroughly studied than melanoma, it is clear that nevi and melanoma share common driver mutations. Acquired melanocytic nevi harbor oncogenic mutations in BRAF, which is the predominant oncogene associated with melanoma. Congenital melanocytic nevi and blue nevi frequently harbor NRAS mutations and GNAQ mutations, respectively, while Spitz and atypical Spitz tumors often exhibit HRAS and kinase rearrangements. These initial 'driver' mutations are thought to trigger the establishment of benign nevi. After this initial phase of the cell proliferation, a senescence program is executed, causing termination of nevi growth. Only upon the emergence of additional tumorigenic alterations, which may provide an escape from oncogene-induced senescence, can malignant progression occur. Here, we review the current literature on the pathobiology and genetics of nevi in the hope that additional studies of nevi promise to inform our understanding of the transition from benign neoplasm to malignancy.
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            Melanomas of childhood.

            S M Spitz (1948)
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              Update on dermoscopy of Spitz/Reed naevi and management guidelines by the International Dermoscopy Society.

              Spitzoid lesions represent a challenging and controversial group of tumours, in terms of clinical recognition, biological behaviour and management strategies. Although Spitz naevi are considered benign tumours, their clinical and dermoscopic morphological overlap with spitzoid melanoma renders the management of spitzoid lesions particularly difficult. The controversy deepens because of the existence of tumours that cannot be safely histopathologically diagnosed as naevi or melanomas (atypical Spitz tumours). The dual objective of the present study was to provide an updated classification on dermoscopy of Spitz naevi, and management recommendations of spitzoid-looking lesions based on a consensus among experts in the field. After a detailed search of the literature for eligible studies, a data synthesis was performed from 15 studies on dermoscopy of Spitz naevi. Dermoscopically, Spitz naevi are typified by three main patterns: starburst pattern (51%), a pattern of regularly distributed dotted vessels (19%) and globular pattern with reticular depigmentation (17%). A consensus-based algorithm for the management of spitzoid lesions is proposed. According to it, dermoscopically asymmetric lesions with spitzoid features (both flat/raised and nodular) should be excised to rule out melanoma. Dermoscopically symmetric spitzoid nodules should also be excised or closely monitored, irrespective of age, to rule out atypical Spitz tumours. Dermoscopically symmetric, flat spitzoid lesions should be managed according to the age of the patient. Finally, the histopathological diagnosis of atypical Spitz tumour should warrant wide excision but not a sentinel lymph-node biopsy.
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                Author and article information

                Journal
                Dermatol Pract Concept
                Dermatol Pract Concept
                DP
                Dermatology Practical & Conceptual
                Mattioli 1885
                2160-9381
                January 2023
                01 January 2023
                : 13
                : 1
                : e2023041
                Affiliations
                [1 ]Ospedale Santa Maria della Speranza, Battipaglia, Italy
                [2 ]Dermatology Unit, University of Campania, Naples, Italy
                [3 ]Dermatology Section- Instituto de Investigaciones Médicas Universidad de Buenos Aires, Argentina
                [4 ]Dermatology Unit, University “Federico II”, Naples, Italy
                [5 ]AORN Santobono – Pausilipon, Naples, Italy
                [6 ]Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Skin Cancer Unit, Meldola (FC), Italy
                [7 ]Department of Dermatology Centre Hospitalier Lyon Sud, France
                [8 ]Lyons cancer research center UMR INSERM U1052 - CNRS5286 - UCBL1, France
                [9 ]Lyon 1 University, France
                Author notes
                Corresponding Author: Gabriella Brancaccio, MD, Dermatology Unit, University of Campania, Via Pansini 5, 80131, Napoli, Italy. E-mail: gabri.brancaccio@ 123456gmail.com
                Article
                2547dp1301a41
                10.5826/dpc.1301a41
                9946083
                8ba777b3-8dd3-4e33-a05c-680e26c3bd05
                ©2023 Brunetti et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (BY-NC-4.0), https://creativecommons.org/licenses/by-nc/4.0/, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original authors and source are credited.

                History
                : 04 July 2022
                Categories
                Original Article

                spitz nevus,starburst,stardust
                spitz nevus, starburst, stardust

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