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光化性角化病的组织学局灶内异质性与癌化域有关。

Histological intralesional heterogeneity of actinic keratoses relates to field cancerization.

机构信息

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

CentroDerm Clinic, Heinz-Fangman-Strasse 57, Wuppertal, Germany.

出版信息

J Dtsch Dermatol Ges. 2018 Oct;16(10):1211-1217. doi: 10.1111/ddg.13658. Epub 2018 Sep 24.

Abstract

BACKGROUND/OBJECTIVES: Histological heterogeneity within distinct actinic keratosis (AK) lesions has been described and might serve as an additional feature of AKs. We aimed to investigate and quantify the histological heterogeneity of AKs regarding different grading systems.

METHODS AND MATERIAL

We assessed the histology of 3 mm biopsies of AK lesions located on the scalp or face. We documented basal proliferation (PRO I-III), histological grade (AK I-III) and determined the overall classification of each lesion.

RESULTS

Of the 305 lesions included, 48 (15.7 %) lesions were classified as AK I, 152 (49.8 %) as AK II and 105 (34.4 %) as AK III. 33 AKs (10.8 %) showed no basal proliferation, 94 (30.8 %) were graded as PRO I, 99 (32.5 %) as PRO II and 79 (25.9 %) as PRO III. One histological grade and basal growth pattern per lesion was observed in 94 (30.8 %) and 104 (34.1 %) cases respectively, two grades in 170 (55.7 %) and 168 (55.1 %) cases, and three grades in 41 (13.4 %) and 33 (10.8 %) cases (Chi-squared test, p < 0.0001).

CONCLUSIONS

By analogy with the clinical heterogeneity of field cancerization, AKs show a high histological grade heterogeneity even within small lesions. Variations in AK grading reflect the heterogeneity of the cancerization field and might serve as additional feature.

摘要

背景/目的:已描述不同光化性角化病(AK)病变内的组织学异质性,且其可能是 AK 的另一个特征。我们旨在针对不同分级系统,研究和量化 AK 的组织学异质性。

方法和材料

我们评估了头皮或面部 AK 病变 3mm 活检的组织学。我们记录了基底细胞增生(PRO I-III)、组织学分级(AK I-III),并确定了每个病变的整体分类。

结果

在纳入的 305 个病变中,48 个(15.7%)病变被归类为 AK I,152 个(49.8%)为 AK II,105 个(34.4%)为 AK III。33 个 AK(10.8%)无基底细胞增生,94 个(30.8%)分级为 PRO I,99 个(32.5%)为 PRO II,79 个(25.9%)为 PRO III。每个病变分别观察到一个组织学分级和基底生长模式(分别为 94 个[30.8%]和 104 个[34.1%])、两个分级(分别为 170 个[55.7%]和 168 个[55.1%])和三个分级(分别为 41 个[13.4%]和 33 个[10.8%])(卡方检验,p<0.0001)。

结论

与临床的“癌化领域”异质性类似,AK 即使在小病变中也表现出很高的组织学分级异质性。AK 分级的变化反映了癌化领域的异质性,且其可能是另一个特征。

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