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用于评估光化性角化病严重程度的临床、皮肤镜及共聚焦显微镜检查评分的比较分析

Comparative Analysis of Clinical, Dermoscopic, and Confocal Microscopy Scores for Assessing Severity of Actinic Keratosis.

作者信息

Soare Cristina, Cozma Elena Codruța, Giurcăneanu Călin, Voiculescu Vlad Mihai

机构信息

Department of Dermato-Oncology, Faculty of Medicine, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.

Department of Dermatology, "Elias" University Emergency Hospital, 011461 Bucharest, Romania.

出版信息

Cancers (Basel). 2025 Sep 3;17(17):2899. doi: 10.3390/cancers17172899.

DOI:10.3390/cancers17172899
PMID:40940996
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12428301/
Abstract

: Actinic keratosis (AK) is a common UV-induced intraepidermal neoplasm and a precursor to cutaneous squamous cell carcinoma (cSCC). Accurate, non-invasive assessment of AK severity is crucial for early intervention and risk stratification. Objective: To evaluate the relationship between clinical severity of AK, as defined by the Olsen grading scale, and predefined dermoscopic and reflectance confocal microscopy (RCM) features. : This cross-sectional study enrolled 50 patients with clinically diagnosed AK at a tertiary dermatology center between April 2024 and July 2025. Each lesion was assessed clinically using the Olsen scale (grades 1-3), dermoscopically (five features scored 0-3; total score 0-15), and via RCM (five RCM parameters scored 0-3; total score 0-15). Statistical correlations between clinical grade and imaging features were analyzed using Pearson's χ test with effect size metrics. : Diffuse erythema ( < 0.001), micro-erosions ( = 0.002), strawberry pattern ( = 0.038), and scales ( = 0.012) correlated significantly with Olsen grade, whereas vessels ( = 0.566) did not. All five RCM parameters showed strong associations with clinical severity. Composite dermoscopic and RCM scores correlated with Olsen grade (both < 0.001). Abnormal honeycomb pattern, parakeratosis, inflammation, and solar elastosis were the best RCM predictors of high dermoscopic severity (all < 0.001); conversely, erosions, erythema, and scales were the strongest dermoscopic predictors of high RCM severity (all < 0.001). : This study demonstrates strong, statistically significant associations between clinical, dermoscopic, and confocal features of AK. This supports the integration of multimodal scoring into unified AK severity frameworks.

摘要

光化性角化病(AK)是一种常见的紫外线诱导的表皮内肿瘤,也是皮肤鳞状细胞癌(cSCC)的前驱病变。准确、无创地评估AK的严重程度对于早期干预和风险分层至关重要。目的:评估由奥尔森分级量表定义的AK临床严重程度与预先定义的皮肤镜和反射式共聚焦显微镜(RCM)特征之间的关系。:这项横断面研究于2024年4月至2025年7月在一家三级皮肤科中心纳入了50例临床诊断为AK的患者。每个病变均使用奥尔森量表(1 - 3级)进行临床评估,通过皮肤镜(五个特征评分为0 - 3分;总分0 - 15分)以及通过RCM(五个RCM参数评分为0 - 3分;总分0 - 15分)进行评估。使用Pearson卡方检验及效应量指标分析临床分级与影像特征之间的统计相关性。:弥漫性红斑(<0.001)、微糜烂(=0.002)、草莓样图案(=0.038)和鳞屑(=0.012)与奥尔森分级显著相关,而血管(=0.566)则无相关性。所有五个RCM参数均与临床严重程度显示出强关联。综合皮肤镜和RCM评分与奥尔森分级相关(均<0.001)。异常蜂巢样图案、角化不全、炎症和日光性弹力纤维变性是皮肤镜高严重程度的最佳RCM预测指标(均<0.001);相反,糜烂、红斑和鳞屑是RCM高严重程度最强的皮肤镜预测指标(均<0.001)。:本研究证明了AK的临床、皮肤镜和共聚焦特征之间存在强的、具有统计学意义的关联。这支持将多模式评分整合到统一的AK严重程度框架中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a18/12428301/a5e29b59ee61/cancers-17-02899-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a18/12428301/a5bd5a717f34/cancers-17-02899-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a18/12428301/9b86b0fc3628/cancers-17-02899-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a18/12428301/a5e29b59ee61/cancers-17-02899-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a18/12428301/a5bd5a717f34/cancers-17-02899-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a18/12428301/9b86b0fc3628/cancers-17-02899-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a18/12428301/a5e29b59ee61/cancers-17-02899-g004.jpg

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本文引用的文献

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Clin Cosmet Investig Dermatol. 2025 Jun 3;18:1359-1373. doi: 10.2147/CCID.S521416. eCollection 2025.
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The clinical value of reflectance confocal microscopy in monitoring treatment of actinic keratosis: A systematic review.反射式共聚焦显微镜在光化性角化病治疗监测中的临床价值:一项系统评价。
Photodiagnosis Photodyn Ther. 2025 Jun;53:104539. doi: 10.1016/j.pdpdt.2025.104539. Epub 2025 Mar 1.
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riSCC: A personalized risk model for the development of poor outcomes in cutaneous squamous cell carcinoma.
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