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[白癜风样色素脱失与重度特应性皮炎。附4例报告]

[Vitiligoid achromias and severe atopic dermatitis. Apropos of 4 cases].

作者信息

Larrègue M, Martin J, Bressieux J M, Canuel C, De Giacomoni P, Ramdenée P, Babin P

出版信息

Ann Dermatol Venereol. 1985;112(8):589-600.

PMID:4096464
Abstract

Four patients with important and disabling atopic dermatitis persisting during adulthood have presented leucodermia in certain areas of eczema. As melanosomes and melanocytes have totally disappeared in these regions, this depigmentation corresponds thus to an achromia. Clinically, we noted macular achromia with hyperpigmented border of special topography since touching pleat regions initially present eczema lesions: anterior face of wrists and footnecks. Slight lichenification is noted in achromic regions. In spite of many analogies with vitiligo, we differentiate this achromia from vitiligo on the basis of absence of familial post-history and absence of new localisations after 5 to 6 years cause. A review of depigmentations described during atopic dermatitis does not show similar facts. Depigmentation induced by local steroid therapy does not give such clinical and ultrastructural aspects. In 3 patients, there was no local application of depigmenting agent. In one case, 8-oxyquinoleine was applied transiently. Vitiliginous achromias of pleat regions initially presenting important atopic dermatitis are probably due to multifactorial factors: possible factors are inflammation and secondary epidermal modification due to local steroid therapy and may be some excipients. Being a rare situation in atopy, we have registered it only 14 times in 860 followed atopic dermatitis. The study of series of atopic dermatitis followed on a long-term basis should allow to evaluate the frequency of such incidents and the respective role of aetiological factors with we suspect.

摘要

4例成年期持续存在严重且致残性特应性皮炎的患者在湿疹的某些区域出现了白斑。由于这些区域的黑素小体和黑素细胞已完全消失,因此这种色素脱失相当于色素缺乏症。临床上,我们注意到在最初出现湿疹病变的接触褶皱区域(手腕前侧和足颈)有特殊形态的边界色素沉着的斑状色素缺乏。在色素缺乏区域有轻微苔藓化。尽管与白癜风有许多相似之处,但基于无家族病史以及发病5至6年后无新的色素脱失部位,我们将这种色素缺乏症与白癜风区分开来。对特应性皮炎期间描述的色素脱失的回顾未显示类似情况。局部类固醇治疗引起的色素脱失不会出现这样的临床和超微结构表现。3例患者未局部应用色素脱失剂。1例患者曾短暂应用过8-羟基喹啉。最初表现为严重特应性皮炎的褶皱区域的白癜风样色素缺乏可能是多因素导致的:可能的因素包括炎症、局部类固醇治疗引起的继发性表皮改变以及可能的一些辅料。作为特应性疾病中的罕见情况,在860例随访的特应性皮炎患者中我们仅记录到14例。对长期随访的特应性皮炎系列病例的研究应能评估此类事件的发生率以及我们怀疑的病因因素各自的作用。

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