Clinical and Dermoscopic Studying of Palmoplantar Keratodermas

Atul Rajeendran, M. M. Shenoy, Malcolm Pinto, Vishal B Amin, S. Hegde, Amina Asfiya, A. Razak
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Abstract

Background: Palmoplantar keratodermas (PPK) represents a group of skin disorders characterized by excessive epidermal thickening of palms and soles. They are classically divided into inherited and acquired groups. Dermoscopy is a non-invasive procedure that can aid in the clinical diagnosis of PPK. Objectives: To study the clinical features and dermoscopic patterns of PPK caused by various dermatological conditions. Methods: Ninety-eight patients with various types of PPK were included in this cross-sectional observational study after obtaining informed consent. Symptoms, general systemic findings, and dermatological manifestations were recorded. The dermoscopic examination was performed by a single observer using Heine Delta 20+ and FotoFinder Medicam 1000. Diagnostically challenging cases were biopsied for histopathological examination. SPSS (Statistical Package for Social Sciences) version 20 [IBM SPSS statistics (IBM Corp. Armonk, NY, USA released 2011)] was used to perform statistical analyses. The chi-square test was applied to examine statistical associations between qualitative variables. The level of significance was set at 5%. Results: Out of 98 cases with PPK, 93 were acquired, and 5 were inherited. The commonest dermoscopy pattern included palmoplantar psoriasis (n = 48), showing a background light red color with yellow diffused white scales with regular dotted and glomerular vessels, followed by palmoplantar eczema (n = 39) (light red color with yellow patchy white background, yellow scales, and patchy dotted vessels). Light red/dull red background with diffuse white scaling and regular linear, dotted, or glomerular vessels were significantly in favor of palmoplantar psoriasis, while a yellow background, diffuse yellow scaling, patchy dotted vessels, and yellow crust were more in favor of palmoplantar dermatitis. Pityriasis rubra pilaris (PRP) (n = 3) showed a light red background, diffused white scales, and dotted and linear vessels with patchy distribution. Lichen planus (n = 2) revealed a light red color with a yellow background, diffused and peripheral white scales, and irregular linear (radial) and dotted vessels. Wickham’s striae were found on palms. Tinea manuum with pedis (n = 1) showed a dull red background and diffused white and yellow scales with the localization of the scales in the skin furrows. PPK secondary to ichthyosis vulgaris (n = 3) revealed a light red background with diffused white and yellow patchy scaling and regular linear and patchy glomerular vessels. Greither’s disease showed a light red color with a yellow background, a diffused white scale pattern, and multiple dotted vessels arranged in an irregular pattern. Erythrokeratodermia variabilis showed a background color of light red and diffused white scales in a crisscross pattern. Conclusions: Dermoscopy can reveal characteristic but not pathognomonic dermoscopic patterns that can be useful in the clinical diagnosis of various types of PPK. More studies with larger sample sizes may help validate these findings and identify new patterns.
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掌跖角化病的临床和皮肤镜研究
背景:掌跖角化病(PPK)是一组以手掌和足底表皮过度增厚为特征的皮肤病。它们通常分为遗传性和获得性两类。皮肤镜检查是一种非侵入性检查方法,有助于 PPK 的临床诊断。研究目的研究各种皮肤病引起的 PPK 的临床特征和皮肤镜模式。方法在获得知情同意后,98 名患有各种类型 PPK 的患者被纳入这项横断面观察性研究。研究记录了患者的症状、全身检查结果和皮肤病表现。皮肤镜检查由一名观察者使用 Heine Delta 20+ 和 FotoFinder Medicam 1000 进行。对诊断困难的病例进行活组织病理学检查。使用 SPSS(社会科学统计软件包)第 20 版[IBM SPSS statistics (IBM Corp. Armonk, NY, USA released 2011)]进行统计分析。定性变量之间的统计关联采用卡方检验。显著性水平设定为 5%。结果在 98 例 PPK 患者中,93 例为获得性,5 例为遗传性。最常见的皮肤镜检查模式包括掌跖银屑病(48 例),表现为浅红色背景,黄色弥漫性白色鳞屑,有规则的点状和团状血管,其次是掌跖湿疹(39 例)(浅红色背景,黄色斑块状白色背景,黄色鳞屑,斑块状点状血管)。浅红色/暗红色背景,伴有弥漫性白色鳞屑和规则的线状、点状或肾小球状血管的人明显更倾向于掌跖银屑病,而黄色背景、弥漫性黄色鳞屑、斑点状点状血管和黄色结痂的人更倾向于掌跖皮炎。掌跖红皮病(PRP)(n = 3)表现为浅红色背景、弥漫性白色鳞屑、点状和线状血管斑块分布。扁平苔藓(n = 2)呈淡红色,黄底,弥漫性和周边白色鳞屑,不规则的线状(放射状)和点状血管。手掌上有威克姆条纹。足癣(n = 1)表现为暗红色背景、弥漫性白色和黄色鳞屑,鳞屑位于皮肤沟内。继发于寻常型鱼鳞病的 PPK(3 例)表现为淡红色背景,弥漫性白色和黄色斑片状鳞屑,以及规则的线状和斑片状肾小球血管。格雷氏病表现为淡红色,黄底,弥漫性白色鳞屑,多条点状血管排列不规则。变异性红斑角化症的皮肤底色为淡红色,弥漫性白色鳞屑呈纵横交错状。结论:皮肤镜检查可以显示出特征性的皮肤镜模式,但不是病理诊断模式,可用于各种类型的 PPK 的临床诊断。更多样本量更大的研究可能有助于验证这些发现并找出新的模式。
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