Non-multiple medium-sized congenital melanocytic nevi: to excise or to follow up?

IF 1.4 4区 医学 Q3 ALLERGY Postepy Dermatologii I Alergologii Pub Date : 2023-08-01 DOI:10.5114/ada.2023.128718
Mateusz K Mateuszczyk, Karolina Świerczyńska-Mróz, Iwona Chlebicka, Jacek C Szepietowski
{"title":"Non-multiple medium-sized congenital melanocytic nevi: to excise or to follow up?","authors":"Mateusz K Mateuszczyk,&nbsp;Karolina Świerczyńska-Mróz,&nbsp;Iwona Chlebicka,&nbsp;Jacek C Szepietowski","doi":"10.5114/ada.2023.128718","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Congenital melanocytic nevi (CMN) are benign lesions composed of clonal proliferations of melanocytes. Although medium-sized CMN are common and generally remain benign throughout a person's lifetime, they may be precursors of melanoma. There is a limited number of studies focused on the risk of melanoma in solitary, medium-sized, congenital melanocytic nevus; therefore, the incidence of malignant transformation and guidelines for treatment are not well established.</p><p><strong>Aim: </strong>Prompted by the limited data, we conducted this study to gather more information about medium-sized CMN, to optimize clinical care. We share our analysis of surgically removed medium-sized CMN.</p><p><strong>Material and methods: </strong>A total of 10 patients with non-multiple, medium-sized, congenital melanocytic nevus were included in this study. Lesions were removed using surgical procedures.</p><p><strong>Results: </strong>In most of the cases the reason for excision of the medium-sized CMN was evolution of the lesion or aesthetic considerations reported by the patients. In 2 cases, due to the large size of the lesions, serial excisions were performed, while other CMN were removed surgically using simple excision technique. Eight of 10 medium-sized CMN were histologically described as benign, and 2 cases of malignant transformations were reported.</p><p><strong>Conclusions: </strong>According to our clinical experience and knowledge, we recommend managing patients on an individual basis, taking into consideration multiple clinical attributes. In our opinion, long-lasting observation is the management of choice, and if there is need of surgery, we recommend total simple or staged excision depending on nevus size.</p>","PeriodicalId":54595,"journal":{"name":"Postepy Dermatologii I Alergologii","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3e/5f/PDIA-40-50865.PMC10485756.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Postepy Dermatologii I Alergologii","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5114/ada.2023.128718","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Congenital melanocytic nevi (CMN) are benign lesions composed of clonal proliferations of melanocytes. Although medium-sized CMN are common and generally remain benign throughout a person's lifetime, they may be precursors of melanoma. There is a limited number of studies focused on the risk of melanoma in solitary, medium-sized, congenital melanocytic nevus; therefore, the incidence of malignant transformation and guidelines for treatment are not well established.

Aim: Prompted by the limited data, we conducted this study to gather more information about medium-sized CMN, to optimize clinical care. We share our analysis of surgically removed medium-sized CMN.

Material and methods: A total of 10 patients with non-multiple, medium-sized, congenital melanocytic nevus were included in this study. Lesions were removed using surgical procedures.

Results: In most of the cases the reason for excision of the medium-sized CMN was evolution of the lesion or aesthetic considerations reported by the patients. In 2 cases, due to the large size of the lesions, serial excisions were performed, while other CMN were removed surgically using simple excision technique. Eight of 10 medium-sized CMN were histologically described as benign, and 2 cases of malignant transformations were reported.

Conclusions: According to our clinical experience and knowledge, we recommend managing patients on an individual basis, taking into consideration multiple clinical attributes. In our opinion, long-lasting observation is the management of choice, and if there is need of surgery, we recommend total simple or staged excision depending on nevus size.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
非多发中型先天性黑素细胞痣:切除还是随访?
简介:先天性黑素细胞痣(CMN)是由黑素细胞克隆性增生组成的良性病变。虽然中等大小的CMN很常见,并且在人的一生中通常是良性的,但它们可能是黑色素瘤的前兆。有有限数量的研究集中在孤立的,中等大小的,先天性黑素细胞痣的黑色素瘤的风险;因此,恶性转化的发生率和治疗指南尚未很好地确定。目的:由于资料有限,本研究旨在收集更多关于中型CMN的信息,以优化临床护理。我们分享我们对手术切除的中型CMN的分析。材料和方法:本研究共纳入10例非多发、中等大小的先天性黑素细胞痣。病变通过外科手术切除。结果:在大多数病例中,切除中型CMN的原因是病变的演变或患者报告的美学考虑。2例因病变较大,行连续切除,其余CMN均行单纯切除。10个中型CMN中有8个在组织学上被描述为良性,2例被报道为恶性转化。结论:根据我们的临床经验和知识,我们建议对患者进行个体化管理,考虑多种临床属性。我们认为,长期观察是治疗的选择,如果需要手术,我们建议根据痣的大小进行简单或分期切除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
2.60
自引率
7.10%
发文量
107
审稿时长
6-12 weeks
期刊介绍: Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii is a bimonthly aimed at allergologists and dermatologists.
期刊最新文献
Association between single nucleotide polymorphisms of interleukin-35 genes and atopic dermatitis. Cannabidiol modulation of immune cell function: in vitro insights and therapeutic implications for atopic dermatitis. Delayed drug hypersensitivity to anti-tuberculosis drug: a new desensitization scheme. Dermatophagoides pteronyssinus proteins and their role in the diagnostics and management of house dust mite allergy: exploring allergenic components. Hidradenitis suppurativa: a new therapeutic approach for an old disease.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1