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治疗抵抗性光化性角化病的特征为明显的临床和组织学特征。

Treatment-resistant actinic keratoses are characterized by distinct clinical and histological features.

机构信息

Department of Dermatology, Venereology and Allergology, Ruhr-University, Bochum, Germany -

Institute of Dermatopathology, MVZ Corius DermPathBonn, Bonn, Germany -

出版信息

Ital J Dermatol Venerol. 2021 Apr;156(2):213-219. doi: 10.23736/S2784-8671.21.06892-9.

Abstract

BACKGROUND

Actinic keratoses (AK) are generally treated to reduce the risk of progression into invasive cutaneous squamous cell carcinoma (cSCC). However, this risk of transformation is low, and rather than focusing on these lesions, current treatment studies report on complete clearance of AKs in an entire field. This study aimed to investigate treatment-resistant AKs (trAK) after field therapy compared to randomly chosen AKs prior to treatment.

METHODS

AKs were clinically assessed according to the grade of hyperkeratosis and pain on palpation, prior to treatment. TrAKs were biopsied and compared to AKs which were biopsied prior to any treatment. AKs were evaluated regarding histological severity (AKI-III), their basal growth grading (PROI-III), acantholysis, elastosis, follicular extension of atypical keratinocytes and accompanying infiltrate.

RESULTS

Two hundred eleven AKs in 171 patients were identified. TrAKs (N.=79) were significantly more painful (64.6% vs. 22.0%; P<0.0001), showing acantholysis (57.0% vs. 33.3%; P=0.0007); and with distinct basal proliferation (PROIII) (64.4% vs. 46.2%; P=0.0099) compared to the control group (N.=132). In a multivariate analysis using logistic regression, pain and PRO III graded lesions were significant independent (P<0.0001 and P=0.0179) predictors for trAKs. Focusing on individual histological features in the trAK group, AKs with grade AKIII, PROIII or follicular extension reaching the sebaceous gland were the most common findings with 51.9%, 64.6%, and 59.5% AKs demonstrating this, respectively.

CONCLUSIONS

TrAKs are often painful, showing a distinct basal proliferation (PROIII) and acantholysis. As these features are also seen in invasive cSCCs, trAKs may represent a subgroup of AKs and, for this reason, it requires further evaluations.

摘要

背景

光化性角化病(AK)通常通过治疗来降低进展为侵袭性皮肤鳞状细胞癌(cSCC)的风险。然而,这种转化风险较低,与其专注于这些病变,不如将当前的治疗研究报告集中在整个病灶中 AK 的完全清除上。本研究旨在调查与治疗前随机选择的 AK 相比,在病灶治疗后出现的治疗抵抗性 AK(trAK)。

方法

在治疗前,根据角化过度和触诊疼痛程度对 AK 进行临床评估。对 trAK 进行活检,并与任何治疗前活检的 AK 进行比较。评估 AK 的组织学严重程度(AKI-III)、基底生长分级(PROI-III)、棘层松解、弹性组织变性、异常角质形成细胞的毛囊延伸和伴随的浸润。

结果

在 171 名患者中发现了 211 个 AK。trAK(n=79)明显更痛(64.6%比 22.0%;P<0.0001),表现出棘层松解(57.0%比 33.3%;P=0.0007)和明显的基底增殖(PROIII)(64.4%比 46.2%;P=0.0099),与对照组(n=132)相比。在使用逻辑回归的多变量分析中,疼痛和 PRO III 分级病变是 trAK 的显著独立预测因子(P<0.0001 和 P=0.0179)。在 trAK 组中,关注个别组织学特征,具有 AKIII、PROIII 或延伸至皮脂腺的毛囊分级的 AK 最常见,分别有 51.9%、64.6%和 59.5%的 AK 表现出这种特征。

结论

trAK 通常是疼痛的,表现出明显的基底增殖(PROIII)和棘层松解。由于这些特征也见于侵袭性 cSCC,trAK 可能代表 AK 的一个亚组,因此需要进一步评估。

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