Parallel pigmented network in lentigo maligna: a case series and correlation with in vivo reflectance confocal microscopy

恶性痣 医学 共焦 共焦显微镜 皮肤病科 反射率 体内 显微镜 病理 光学 黑色素瘤 生物 癌症研究 物理 生物技术
作者
Giulia Greta Dradi,R. Gamo,María Uxmal Floristán Murzubal,Fernando Pinedo,C. Sarró-Fuente,J.L. López‐Estebaranz
出处
期刊:European Journal of Dermatology [John Libbey Eurotext]
卷期号:34 (5): 490-496
标识
DOI:10.1684/ejd.2024.4747
摘要

Lentigo maligna (LM) often poses a diagnostic challenge due to its clinical and dermoscopic mimicry of benign lesions, leading to delayed diagnosis. Focal areas of reticular disruption have been described as one of the earliest dermoscopic signs observed. To describe a novel dermoscopic sign in LM, namely the presence of a parallel pigmented network. Case series of 22 histopathologically-proven LM and lentigo maligna melanoma (LMM), diagnosed between 2018 and 2023, at a tertiary centre. All lesions showed a parallel network upon dermoscopy, in the form of parallel reticular lines, light or dark brown in colour, not emanating from the follicle, with an asymmetrical distribution. Reflectance confocal microscopy (RCM) images were reviewed to correlate these areas. The median age of patients was 73 years old. The majority of lesions were in situ (91%) and extrafacial (82%). Lesions showed minimal signs of atypia other than a parallel network and mostly focal erased areas (100%), followed by perifollicular linear projections (18%) and asymmetrical follicular pigmentation (18%). On RCM, focally areas correlated with atypical junctional thickenings distributed in a parallel fashion (100%) and mitochondria-like structures (23%). Most cases (88%) showed atypical cells in the epidermis, mostly in the form of isolated dendritic cells (41%). Parallel network emerges as a potential dermoscopic sign associated with LM. We hypothesize that in early stages of LM transformation, disruption of the reticular network manifests as parallel lines and/or radial perifollicular lines. Validation with larger studies is warranted.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
建议保存本图,每天支付宝扫一扫(相册选取)领红包
实时播报
zyx发布了新的文献求助10
刚刚
JD完成签到 ,获得积分10
1秒前
今后应助Someone采纳,获得10
1秒前
Lili完成签到,获得积分10
1秒前
琪琪完成签到,获得积分10
1秒前
酷波er应助橘子屿布丁采纳,获得80
1秒前
凌兰完成签到 ,获得积分10
2秒前
学习中的呜哩哇啦完成签到,获得积分10
2秒前
乐天儿发布了新的文献求助10
2秒前
ZJH完成签到 ,获得积分10
2秒前
小张z完成签到,获得积分10
3秒前
111完成签到,获得积分20
3秒前
酷波er应助Xin宇采纳,获得10
4秒前
Hipchengi完成签到,获得积分10
5秒前
AuB发布了新的文献求助10
5秒前
wzy完成签到 ,获得积分10
6秒前
safeheart完成签到,获得积分10
6秒前
6秒前
ahgihnb发布了新的文献求助10
6秒前
超级Huan完成签到,获得积分10
7秒前
7秒前
慕青应助zhanghao采纳,获得30
8秒前
8秒前
柠檬不萌完成签到,获得积分10
9秒前
kk完成签到,获得积分20
9秒前
10秒前
三点半发布了新的文献求助10
10秒前
11秒前
11秒前
Robin完成签到,获得积分10
11秒前
Recho完成签到 ,获得积分10
12秒前
12秒前
keyanrubbish完成签到,获得积分10
12秒前
文光完成签到,获得积分10
13秒前
糊涂的麦片完成签到,获得积分10
13秒前
991256发布了新的文献求助10
14秒前
艾欧勾勾完成签到 ,获得积分10
14秒前
xx-xxx发布了新的文献求助10
16秒前
Akim应助小鱼采纳,获得10
16秒前
wqa1472完成签到,获得积分10
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
List of 1,091 Public Pension Profiles by Region 1041
Mentoring for Wellbeing in Schools 1000
Binary Alloy Phase Diagrams, 2nd Edition 600
Atlas of Liver Pathology: A Pattern-Based Approach 500
A Technologist’s Guide to Performing Sleep Studies 500
EEG in Childhood Epilepsy: Initial Presentation & Long-Term Follow-Up 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5494790
求助须知:如何正确求助?哪些是违规求助? 4592530
关于积分的说明 14437544
捐赠科研通 4525391
什么是DOI,文献DOI怎么找? 2479374
邀请新用户注册赠送积分活动 1464191
关于科研通互助平台的介绍 1437185