Reviewing Challenges in the Diagnosis and Treatment of Lentigo Maligna and Lentigo-Maligna Melanoma.

Rare cancers and therapy Pub Date : 2015-01-01 Epub Date: 2015-10-15 DOI:10.1007/s40487-015-0012-9
Margit L W Juhász, Ellen S Marmur
{"title":"Reviewing Challenges in the Diagnosis and Treatment of Lentigo Maligna and Lentigo-Maligna Melanoma.","authors":"Margit L W Juhász,&nbsp;Ellen S Marmur","doi":"10.1007/s40487-015-0012-9","DOIUrl":null,"url":null,"abstract":"<p><p>Lentigo maligna (LM) and lentigo-maligna melanoma (LMM) are pigmented skin lesions that may exist on a continuous clinical and pathological spectrum of melanocytic skin cancer. LM is often described as a \"benign\" lesion and is accepted as a melanoma in situ; LM can undergo malignant transformation to particularly aggressive melanoma. LMM is an invasive melanoma that shares properties of LM, as well as exhibiting the metastatic potential of malignant melanoma. Unfortunately, LM/LMM diagnosis based on dermoscopy is rather ambiguous, and these lesions are often mistaken for junctional dysplastic nevi over sun-damaged skin, pigmented actinic keratosis, solar lentigo, or seborrheic keratosis. Diagnosis must be made on biopsy using distinct dermatopathologic features. These include a pagetoid appearance of melanocytes, melanocyte atypia, non-uniform pigmentation/distribution of melanocytes, and increased melanocyte density in a background of extensive photodamage. Advancements in immunohistochemical staining techniques, including soluble adenylyl cyclase (antibody R21), makes diagnosis easier and allows the definition of borders down to a single cell. After a pathologic diagnosis, there are a variety of treatment options, both surgical and non-surgical. Although surgical removal with a wide excision border is the preferred treatment due to decreased recurrence rates, experimental combination therapies are gaining popularity. However, no matter the treatment, LM/LMM carries a high recurrence rate, and patients must be monitored rigorously for recurrence as well as the appearance of additional skin lesions/cancers.</p>","PeriodicalId":91604,"journal":{"name":"Rare cancers and therapy","volume":"3 ","pages":"133-145"},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s40487-015-0012-9","citationCount":"21","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare cancers and therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s40487-015-0012-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/10/15 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 21

Abstract

Lentigo maligna (LM) and lentigo-maligna melanoma (LMM) are pigmented skin lesions that may exist on a continuous clinical and pathological spectrum of melanocytic skin cancer. LM is often described as a "benign" lesion and is accepted as a melanoma in situ; LM can undergo malignant transformation to particularly aggressive melanoma. LMM is an invasive melanoma that shares properties of LM, as well as exhibiting the metastatic potential of malignant melanoma. Unfortunately, LM/LMM diagnosis based on dermoscopy is rather ambiguous, and these lesions are often mistaken for junctional dysplastic nevi over sun-damaged skin, pigmented actinic keratosis, solar lentigo, or seborrheic keratosis. Diagnosis must be made on biopsy using distinct dermatopathologic features. These include a pagetoid appearance of melanocytes, melanocyte atypia, non-uniform pigmentation/distribution of melanocytes, and increased melanocyte density in a background of extensive photodamage. Advancements in immunohistochemical staining techniques, including soluble adenylyl cyclase (antibody R21), makes diagnosis easier and allows the definition of borders down to a single cell. After a pathologic diagnosis, there are a variety of treatment options, both surgical and non-surgical. Although surgical removal with a wide excision border is the preferred treatment due to decreased recurrence rates, experimental combination therapies are gaining popularity. However, no matter the treatment, LM/LMM carries a high recurrence rate, and patients must be monitored rigorously for recurrence as well as the appearance of additional skin lesions/cancers.

Abstract Image

Abstract Image

Abstract Image

恶性慢斑痣和恶性慢斑痣黑色素瘤的诊断和治疗的挑战。
恶性Lentigo (LM)和Lentigo -恶性黑色素瘤(LMM)是色素沉着的皮肤病变,可能存在于黑色素细胞皮肤癌的连续临床和病理谱上。LM通常被描述为“良性”病变,被认为是原位黑色素瘤;LM可恶性转化为特别具有侵袭性的黑色素瘤。LMM是一种侵袭性黑色素瘤,具有LM的特性,同时也表现出恶性黑色素瘤的转移潜力。不幸的是,基于皮肤镜的LM/LMM诊断是相当模糊的,这些病变经常被误认为是太阳损伤皮肤上的连接发育不良痣、色素光化性角化病、太阳色素体或脂溢性角化病。诊断必须在活检中使用明确的皮肤病理特征。这些包括黑素细胞的页样外观,黑素细胞异型性,黑素细胞不均匀的色素沉着/分布,以及在广泛的光损伤背景下黑素细胞密度增加。免疫组织化学染色技术的进步,包括可溶性腺苷酸环化酶(抗体R21),使诊断更容易,并允许边界定义到单个细胞。病理诊断后,有多种治疗选择,包括手术和非手术。尽管由于复发率降低,广泛切除边界的手术切除是首选的治疗方法,但实验性联合治疗也越来越受欢迎。然而,无论采用何种治疗方法,LM/LMM的复发率都很高,必须严格监测患者的复发情况以及其他皮肤病变/癌症的出现。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信