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      Agminated Acquired Melanocytic Nevi of the Common and Dysplastic Type

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          Abstract

          Dear Editor: 'Agminated' refers to circumscribed grouping of lesions confined to a localized area of the body. Pigmented lesions that have been described as agminated includes melanocytic nevi1, Spitz nevi2, nevi spilus3, blue nevi4, and multiple lentigines5. However, the presence of acquired common and dysplastic nevi (ACDN) arranged in an agminated pattern has not been well-established. Herein, we describe a patient with multiple agminated acquired melanocytic nevi, several of that were histologically characterized as dysplastic nevi. A 16-years-old female presented with multiple irregular moles on her right inguinal area (Fig. 1A). Her parents reported that this cluster of nevi developed at the age of 6 years, and continuously increased in numbers and sizes. No family history of melanoma or multiple moles was present. Physical examinations revealed more than 40 melanocytic nevi clustered in a 5×5 cm skin area on her right inguinal area, where several of these nevi were irregular with variegation of color and a diameter greater than 5 mm (Fig. 1A). No background pigmentation within or surrounding the cluster was noted clinically or even with Wood's light examination. Dermoscopy of the clustered nevi revealed a diffuse patchy reticulation (Fig. 1B). A biopsy from a clinically atypical nevus demonstrated a lentiginous, compound-melanocytic nevus with architectural disorder in the epidermis. In the dermoepidermal junction, the nests of nevus cells were profused in the tips and sides of elongated rete ridges. In the center of the nevus, nests of melanocytes are present in the papillary dermis (Fig. 2A). There were scattered single cells in a lentiginous array without continuous proliferations (Fig. 2A). A few atypical melanocytes with large, irregularly shaped, hyperchromatic nuclei lay individually or within a small group (Fig. 2B). The diagnosis of dysplastic nevi was confirmed by the presence of an architectural disorders and cytologic atypia. Several nevi within the cluster had clinical, dermoscopic, and histologic features which are commonly attributed to dysplastic nevi. Dysplastic nevi have been the subject of ongoing controversy regarding its definition and use of more than 20 years6. It is argued that dysplastic nevi are both acquired and common, and they should be regarded as nothing but common nevi. However, when considering a review article from Elder6, theses lesions have been only significant in relation to melanoma, as stimulants of melanoma, as markers of risks for melanoma, and as potential and occasional actual precursors of melanoma. Therefore, clinical and histological classifications of nevi have the most important purpose of categorizing these lesions so that dysplastic nevi can be distinguished, clinically and histologically, from melanoma. In our patient, the diagnosis of dysplastic nevi was based on the clinical, dermoscopic and histologic features. Agminated dysplastic lesions, similar to our case should be distinguished from other forms of dysplastic nevi, which show a segmental distribution without a definite clustering. Two cases of dysplastic nevi with segmental distributions have been previously reported in the literature7,8. Both of the cases are not being described as agminated, because multiple dysplastic nevi were distributed throughout the patients' upper left quadrant. One thing that deserves the attention of clinicians is that malignant melanoma developed within the lesions of both cases. There still exists much controversy about the presence of agminated ACDN. Marghoob et al.9 and Bragg et al.10 previously reported 5 cases of agminated ACDN. Unlike our case, however, agminated lesions were superimposed on an underlying dysplastic nevus syndrome phenotype in 4 out of 5 cases. In the 2 cases of the 5 reported as agminated ACDN, malignant melanoma did not developed within the agminated lesion, but within the underlying dysplastic nevus syndrome phenotype. The authors believed that agminated ACDN were a new, previously not described, clinical variant of dysplastic nevi. In conclusion, the uncertainty in the biological behaviors of agminated ACDN suggests a strict follow-up for this unusual entity.

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          Most cited references8

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          Dysplastic naevi: an update.

          Dysplastic naevi are clinically atypical and histologically are characterized by architectural disorder and cytological atypia. Their diagnosis is reproducible if criteria and thresholds are agreed upon. They are significant only in relation to melanoma, as simulants of melanoma, as markers of individuals at increased risk of developing melanoma, and as potential and occasional actual precursors of melanoma. Morphologically and biologically, they are intermediate between common naevi and melanoma. Individuals with dysplastic naevi may have deficient DNA repair, and dysplastic naevi lesions are associated with overexpression of pheomelanin, which may lead to increased oxidative damage and increased potential for DNA damage and tumour progression.
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            Agminated Spitz nevi: report of a child with a unique dermatomal distribution.

            Spitz nevi most commonly present as solitary lesions. Multiple agminated Spitz nevi are a rare presentation, with 38 reported cases in the English language literature. We report a 2-year-old girl who presented with multiple Spitz nevi in a unique, dermatome-like distribution and review the English-language literature on agminated Spitz nevi.
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              A case of malignant melanoma arising from an acquired agminated melanocytic naevus.

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                Author and article information

                Journal
                Ann Dermatol
                Ann Dermatol
                AD
                Annals of Dermatology
                Korean Dermatological Association; The Korean Society for Investigative Dermatology
                1013-9087
                2005-3894
                August 2013
                13 August 2013
                : 25
                : 3
                : 380-382
                Affiliations
                Department of Dermatology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
                Author notes
                Corresponding author: Young Min Park, Department of Dermatology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 137-701, Korea. Tel: 82-2-2258-6223, Fax: 82-2-599-9950, yymmpark6301@ 123456hotmail.com
                Article
                10.5021/ad.2013.25.3.380
                3756211
                24003289
                803e29a4-047e-4086-88de-0bdafa88f85b
                Copyright © 2013 The Korean Dermatological Association and The Korean Society for Investigative Dermatology

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 July 2012
                : 26 September 2012
                : 14 October 2012
                Categories
                Letter to the Editor

                Dermatology
                Dermatology

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