模拟鳞状细胞癌的头皮糜烂性脓疱性皮肤病:皮肤镜检查有帮助吗?

IF 2.5 4区 医学 Q2 DERMATOLOGY
Camila Scharf, Aleksandra A Stefaniak, Mario Vaccaro, Francesco Borgia, Federico Vaccaro, Fabrizio Chirico, Andrea Battisti, Valentino Valentini, Giuseppe Argenziano
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摘要

简介:头皮糜烂性脓疱性皮肤病(EPDS)是一种罕见且具有挑战性的皮肤疾病,其特征是头皮上的糜烂,脓疱和结痂病变。诊断EPDS是复杂的,通常会模仿其他皮肤病,如光化性角化病(AK)、基底细胞癌(BCC)或鳞状细胞癌(SCC)。治疗挑战来自EPDS的慢性、复发性,需要长期治疗。目的:本研究旨在鉴别和比较EPDS模拟头皮鳞状细胞癌的皮肤镜特征,以提高诊断准确性和支持无创鉴别。方法:一项回顾性描述性研究,于2017年至2023年在意大利两个皮肤科中心进行,包括43例最初诊断为头皮SCC的患者,随后通过组织学或临床评估和随访确认为EPDS。评估临床和皮肤镜标准。将皮肤镜标准与相同数量的头皮鳞状细胞癌进行比较。结果:共纳入43例患者,以男性为主(42:1)。65%的病例出现雄激素性脱发,主要发生在顶骨区(44%)。发夹状和点状血管,以及白色和混合病变颜色,与SCC密切相关,而多形性和支状血管,橙色色调和靶样毛囊在EPDS中占主导地位。结论:EPDS由于其独特的特点和难以捉摸的病因,给诊断和治疗带来了挑战。区分SCC和EPDS是避免不必要治疗的关键;在这个过程中,皮肤镜可以作为一种工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Erosive Pustular Dermatosis of the Scalp Mimicking Squamous Cell Carcinoma: Can Dermoscopy Be Helpful?

Introduction: Erosive pustular dermatosis of the scalp (EPDS) presents as a rare and challenging skin disorder marked by erosions, pustules, and crusted lesions on the scalp. Diagnosing EPDS is complex, often mimicking other dermatological conditions like actinic keratosis (AK), basal cell carcinoma (BCC), or squamous cell carcinoma (SCC). Therapeutic challenges arise from EPDS's chronic, relapsing nature, which requires long-term management.

Objective: This study aimed to identify and compare dermoscopic features of EPDS mimicking SCC of the scalp to improve diagnostic accuracy and support non-invasive differentiation.

Methods: A retrospective descriptive study, conducted in two Italian dermatological centers from 2017 to 2023, included 43 patients initially diagnosed with SCC of the scalp that was afterwards confirmed as EPDS through either histology or clinical evaluation and follow-up. Clinical and dermoscopic criteria were evaluated. A comparison of dermoscopical criteria with the same number of confirmed SCC of the scalp was performed.

Results: A total of 43 patients were included, predominantly male (42:1). Androgenetic alopecia was present in 65% of cases, predominantly in the parietal area (44%). Hairpin and dotted vessels, along with white and combined lesion colors, were strongly associated with SCC, while polymorphic and branched vessels, orange tones, and targetoid hair follicles predominated in EPDS.

Conclusions: EPDS poses diagnostic and therapeutic challenges due to its unique features and elusive etiology. Distinguishing SCC from EPDS is crucial to avoid unnecessary treatments; dermoscopy can serve as an instrument in this process.

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