面部色素皮损的皮肤镜特征。

ISRN Dermatology Pub Date : 2013-01-01 Epub Date: 2013-02-03 DOI:10.1155/2013/546813
Yana Goncharova, Enas A S Attia, Khawla Souid, Inna V Vasilenko
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引用次数: 34

摘要

四种类型的面部色素皮损(FPSLs)构成了皮肤科医生的诊断挑战;早期脂溢性角化病(SK)、色素光化性角化病(AK)、恶性黄斑(LM)和太阳性黄斑(SL)。回顾性分析64例经组织病理学诊断具有临床挑战性的扁平FPSLs的皮肤镜图像,以确定SK、色素AK、LM和SL各自对应的皮肤镜结果。评估四个主要的皮肤镜特征:清晰的界限、色素模式、滤泡/表皮模式和血管模式。在SK,最具体的皮肤镜特征是滤泡/表皮型(脑状型;100%病变,粟粒样囊肿;50%,粉刺样开口;37.50%),边界分明(54.17%)。AK和LM分别在41.18%和25%的病变中表现为复合特征模式,称为“草莓模式”,其特征为背景红斑和红色伪网络,伴有突出的滤泡开口,周围有白色晕。然而,在LM中,“草莓纹”被假网(87.5%)、均匀无结构色素沉着(75%)和其他维管纹广泛覆盖。在SL中,所有病变均可见无结构的均匀色素沉着(100%)。根据上述数据,我们开发了一种算法来指导FPSLs的皮肤镜特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dermoscopic features of facial pigmented skin lesions.

Dermoscopic features of facial pigmented skin lesions.

Dermoscopic features of facial pigmented skin lesions.

Dermoscopic features of facial pigmented skin lesions.

Four types of facial pigmented skin lesions (FPSLs) constitute diagnostic challenge to dermatologists; early seborrheic keratosis (SK), pigmented actinic keratosis (AK), lentigo maligna (LM), and solar lentigo (SL). A retrospective analysis of dermoscopic images of histopathologically diagnosed clinically-challenging 64 flat FPSLs was conducted to establish the dermoscopic findings corresponding to each of SK, pigmented AK, LM, and SL. Four main dermoscopic features were evaluated: sharp demarcation, pigment pattern, follicular/epidermal pattern, and vascular pattern. In SK, the most specific dermoscopic features are follicular/epidermal pattern (cerebriform pattern; 100% of lesions, milia-like cysts; 50%, and comedo-like openings; 37.50%), and sharp demarcation (54.17%). AK and LM showed a composite characteristic pattern named "strawberry pattern" in 41.18% and 25% of lesions respectively, characterized by a background erythema and red pseudo-network, associated with prominent follicular openings surrounded by a white halo. However, in LM "strawberry pattern" is widely covered by psewdonetwork (87.5%), homogenous structureless pigmentation (75%) and other vascular patterns. In SL, structureless homogenous pigmentation was recognized in all lesions (100%). From the above mentioned data, we developed an algorithm to guide in dermoscopic features of FPSLs.

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