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泰国色素异常性红斑、扁平苔藓色素沉着和色素性接触性皮炎所致色素沉着患者的斑贴试验和组织病理学检查。

Patch testing and histopathology in Thai patients with hyperpigmentation due to Erythema dyschromicum perstans, Lichen planus pigmentosus, and pigmented contact dermatitis.

机构信息

Institue of Dermatology-Ministry of Public Health, Bangkok, Thailand.

出版信息

Asian Pac J Allergy Immunol. 2014 Jun;32(2):185-92. doi: 10.12932/AP0376.32.2.2013.

DOI:10.12932/AP0376.32.2.2013
PMID:25003734
Abstract

BACKGROUND

Erythema dyschromicum perstans (EDP)/Ashy dermatosis (AD), Lichen planus pigmentosus (LPP) and Pigmented contact dermatitis (PCD) are common skin diseases featuring abnormal pigmentation which have overlapping clinical features.

OBJECTIVE

To search for differences in the natural history, clinical features, histopathology and relevant contact allergens in patients those were clinically diagnosed as AD, LPP and PCD in our outpatient clinic.

METHOD

43 patients were enrolled into the study. Patients' demographic details, histological findings, DIF staining, provisional and histology diagnosis were recorded. Closed patch tests with standard fragrance and cosmetic series allergens were performed in all patients.

RESULT

36 of the patients were female and all of them had dark skin complexions (Fitzpatrick's skin type IV-V), as normally found in AD and LPP. The most common histological finding was pigmentary alteration followed by lichenoid infiltration. DIF staining was positive in 6 out of 21 cases, the most common pattern being IgM colloid bodies. Patients with a provisional diagnosis of AD and LPP had positive patch tests in 40 and 36.36% of cases, respectively.

CONCLUSION

We have found some similarities and differences between these 3 clinically and histologically overlapping pigmentary disorder. Clinical history, histopathology and DIF are necessary together for making the diagnosis. Patch testing should be conducted in all cases that present with AD or LPP.

摘要

背景

持久性色素异常性红斑(EDP)/灰泥性皮炎(AD)、色素性扁平苔藓(LPP)和色素性接触性皮炎(PCD)是常见的皮肤疾病,具有异常色素沉着的特征,其临床表现有重叠。

目的

在我们的门诊诊所,对临床诊断为 AD、LPP 和 PCD 的患者,寻找其自然病史、临床特征、组织病理学和相关接触过敏原方面的差异。

方法

共纳入 43 名患者。记录患者的人口统计学资料、组织学发现、DIF 染色、临时和组织学诊断。所有患者均进行标准香料和化妆品系列过敏原的封闭斑贴试验。

结果

36 名患者为女性,均为深色皮肤(Fitzpatrick 皮肤类型 IV-V),这在 AD 和 LPP 中很常见。最常见的组织学发现是色素改变,其次是苔藓样浸润。21 例中有 6 例 DIF 染色阳性,最常见的模式是 IgM 胶体体。临床诊断为 AD 和 LPP 的患者中,分别有 40%和 36.36%的患者斑贴试验阳性。

结论

我们发现这 3 种临床上和组织学上重叠的色素性疾病之间存在一些相似和不同之处。临床病史、组织病理学和 DIF 对于做出诊断是必要的。对于出现 AD 或 LPP 的所有病例,都应进行斑贴试验。

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