不稳定性白癜风病灶周围皮肤的皮肤镜特征:一项横断面研究

C. Chanana, Niti Khunger
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摘要

皮肤镜检查是确定白癜风稳定性的一种非常有用的工具。不稳定型白癜风的皮肤镜特征为三色、彗星尾、星爆、变形虫样、星云样、木薯西米样和毛囊周围色素沉着。大多数研究都是在确定白癜风病变的特征;然而,对正常皮肤的皮肤镜检查却缺乏研究。这将深入了解疾病过程的程度,超越皮肤损伤的边界。我们对100例不稳定白癜风病变进行了研究,并研究了其病灶周围皮肤的皮肤镜特征。本研究的目的是观察不稳定白癜风患者表面正常的皮损周围皮肤的皮肤镜特征。在新德里的一家三级保健中心进行了横断面研究。我们对100例不稳定白癜风病变的病灶周围皮肤进行了1年的评估。病灶周围皮肤被定义为病灶周围5厘米内的区域。皮肤镜使用10倍放大的DERMLITE 4皮肤镜,内置白光和偏振光。偏振光被用来研究色素网络和其他模式的变化。我们寻找诸如色素网络、毛囊周围色素沉着、白斑、微koebner现象和病灶周围皮肤的卫星病变等特征。该研究共包括100个不稳定病变。大多数患者年龄在18 ~ 30岁之间。女性数量超过男性(1.8:1)。所有病例均为进行性疾病,平均病程为12.07±10。85年。白癜风的皮肤镜特征在56%的患者中被观察到,即使是在看起来正常的病灶周围皮肤。最常见的皮肤镜发现是色素网络减少,在33%的病例中可见。毛囊周围色素减退23处,脱色2处,白斑病10处。8个站点出现了微koebners现象。在不稳定的白癜风病例中,病灶周围明显正常的皮肤也显示出疾病活动的迹象。因此,病灶周围的皮肤也应该用皮肤镜仔细检查,局部治疗和有针对性的光疗也应该覆盖看起来正常的病灶周围皮肤,至少在皮肤病变边界5厘米内。重要的是,手术前也应该检查病灶周围的皮肤。
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Dermoscopic Features of Perilesional Skin of Unstable Vitiligo: A Cross-Sectional Study
Dermoscopy is a very useful tool in determining stability in vitiligo. Dermoscopic features of unstable vitiligo are trichrome appearance, comet tail appearance, star burst appearance, amoeboid pattern, nebular pattern, tapioca sago pattern and perifollicular hypopigmentation. Most studies are done on determining features of vitiligo lesions; however, there is lack of studies on dermoscopy in normal appearing perilesional skin. This would give an insight into the extent of the disease process, beyond the borders of skin lesions. We conducted a study on 100 unstable lesions of vitiligo and studied dermoscopic features in its perilesional skin. The objective of this study was to observe dermoscopic features of apparently normal perilesional skin in patients of unstable vitiligo. A cross-sectional study was conducted in a tertiary care centre in New Delhi. We evaluated perilesional skin of 100 unstable vitiligo lesions over a span of 1 year. The perilesional skin has been defined as area within 5 cm of the lesion. Dermoscopy was performed using DERMLITE 4 Dermoscope at 10X magnification with inbuilt white light and polarised light. Polarised light was used to study changes in the pigmentary network and other patterns. We looked for features such as pigment network, perifollicular pigmentation, presence of leukotrichia, microkoebner phenomenon and satellite lesions in the perilesional skin. The study included a total of 100 unstable lesions. Majority of patients belonged to the age group of 18−30 years. Females outnumbered males (1.8:1). All cases had progressive disease and mean duration of disease was 12.07 ± 10. 85 years. Dermoscopic features of vitiligo were observed in 56% of patients even in normal appearing perilesional skin. The most common dermoscopic finding observed was reduced pigment network which was seen in 33% of cases. Perifollicular hypopigmentation and depigmentation were observed in 23 and two sites, respectively, while leukotrichia was seen at ten sites. Eight sites showed microkoebners phenomenon. The perilesional apparently normal skin also shows signs of disease activity in cases of unstable vitiligo. Hence, perilesional skin should also be examined carefully with the dermoscope and topical treatment and targeted phototherapy should aim at covering the normal looking perilesional skin as well, at least within 5 cm of the borders of the skin lesions. Importantly, the perilesional skin should also be examined before surgery.
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