Department of Dermatology, Autoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Medicine Faculty, Department of Dermatology, Ankara University, Ankara, Turkey.
Australas J Dermatol. 2021 Feb;62(1):e55-e61. doi: 10.1111/ajd.13455. Epub 2020 Nov 17.
BACKGROUND/OBJECTIVE: The clinical and dermatoscopic features of lichen planus-like keratosis have been described but the characteristics of this entity in a West-Asian population are not known.
We retrospectively analysed 82 histopathologically verified cases of lichen planus-like keratosis from 81 patients from Iran and Turkey.
The majority of lichen planus-like keratoses were macules (61% n = 50), clinically pigmented (67.1% n = 55) and dermatoscopically multi-coloured (91.5% n = 75). The majority (63.4%) had a single dermatoscopic pattern, most frequently: structureless (35.4%), dots (14.6%) and angulated lines (8.5%). Of the lesions with more than one pattern (n = 30), the majority (n = 21) had asymmetry of pattern, the most common combinations being structureless plus dots (n = 8) and structureless plus angulated lines (n = 5). The most common structure was pigmented dots, most frequently grey and present in 70.7% of cases. Vessels were seen in 30.5% of lesions, being significantly more prevalent in non-pigmented, than pigmented, lichen planus-like keratoses (83.3% vs. 21.4% P < 0.001). When we compared lichen planus-like keratosis in the current study to that entity in a large North American study, the statistically significant differences in a West-Asian population included a greater frequency of pigmented variants, a lower incidence in females and a lower prevalence on the torso, in favour of the face.
Lichen planus-like keratosis in a West-Asian population has clinical and dermatoscopic similarities to that entity in another studied population. The significant differences in gender association and anatomical site may be secondary to cultural factors.
背景/目的:已描述扁平苔藓样角化病的临床和皮肤镜特征,但在西亚人群中这种疾病的特征尚不清楚。
我们回顾性分析了来自伊朗和土耳其的 81 例患者 82 例经组织病理学证实的扁平苔藓样角化病病例。
大多数扁平苔藓样角化病为斑疹(61%,n=50),临床上色素沉着(67.1%,n=55),皮肤镜下多色(91.5%,n=75)。大多数(63.4%)具有单一的皮肤镜模式,最常见的是:无结构(35.4%)、点状(14.6%)和角状线(8.5%)。在具有多种模式的病变中(n=30),大多数(n=21)的模式不对称,最常见的组合是无结构加点状(n=8)和无结构加角状线(n=5)。最常见的结构是色素点状,最常见的是灰色,见于 70.7%的病例。血管见于 30.5%的病变,在非色素性、而非色素性扁平苔藓样角化病中更为常见(83.3%比 21.4%,P<0.001)。当我们将当前研究中的扁平苔藓样角化病与北美大型研究中的这种疾病进行比较时,在西亚人群中,统计学上有意义的差异包括色素性变异的频率更高、女性发病率更低以及躯干上的发病率较低,而面部发病率较高。
西亚人群中的扁平苔藓样角化病在临床和皮肤镜特征上与另一项研究人群中的扁平苔藓样角化病相似。在性别关联和解剖部位上的显著差异可能是文化因素造成的。