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光化性角化病的诊断与治疗。

Diagnosis and therapy of actinic keratosis.

机构信息

Department of Dermatology and Allergology, University Hospital Augsburg, Augsburg, Germany.

出版信息

J Dtsch Dermatol Ges. 2024 May;22(5):675-690. doi: 10.1111/ddg.15288. Epub 2024 Mar 8.

Abstract

Actinic keratosis (AK) is considered a chronic and recurring in situ skin neoplasia, with a possible transformation into invasive squamous cell carcinoma (SCC). Among others, predominant risk factors for development of AK are UV-light exposure and immunosuppression. Basal epidermal keratinocyte atypia (AK I) and proliferation (PRO score) seem to drive malignant transformation, rather than clinical appearance of AK (Olsen I-III). Due to the invasiveness of punch biopsy, those histological criteria are not regularly assessed. Non-invasive imaging techniques, such as optical coherence tomography (OCT), reflectance confocal microscopy (RCM) and line-field confocal OCT (LC-OCT) are helpful to distinguish complex cases of AK, Bowen's disease, and SCC. Moreover, LC-OCT can visualize the epidermis and the papillary dermis at cellular resolution, allowing real-time PRO score assessment. The decision-making for implementation of therapy is still based on clinical risk factors, ranging from lesion- to field-targeted and ablative to non-ablative regimens, but in approximately 85% of the cases a recurrence of AK can be observed after a 1-year follow-up. The possible beneficial use of imaging techniques for a non-invasive follow-up of AK to detect recurrence or invasive progression early on should be subject to critical evaluation in further studies.

摘要

光化性角化病(AK)被认为是一种慢性、复发性原位皮肤肿瘤,有向侵袭性鳞状细胞癌(SCC)转化的可能。紫外线暴露和免疫抑制是 AK 发展的主要危险因素。基底表皮角质形成细胞异型性(AK I)和增殖(PRO 评分)似乎驱动了恶性转化,而不是 AK 的临床表现(Olsen I-III)。由于钻孔活检的侵袭性,这些组织学标准并不经常评估。非侵入性成像技术,如光学相干断层扫描(OCT)、反射共聚焦显微镜(RCM)和线阵共聚焦 OCT(LC-OCT)有助于区分 AK、鲍恩病和 SCC 的复杂病例。此外,LC-OCT 可以以细胞分辨率可视化表皮和乳头真皮,允许实时 PRO 评分评估。治疗方案的决策仍然基于临床危险因素,从病变到区域靶向以及消融性和非消融性方案不等,但在大约 85%的病例中,在 1 年的随访后可观察到 AK 的复发。在进一步的研究中,应批判性地评估成像技术在非侵入性随访 AK 中以早期发现复发或侵袭性进展的可能有益作用。

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