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特发性斑疹性色素沉着症:一例报告并文献复习

Pigmentatio maculosa eruptiva idiopathica: a case report and review of the literature.

作者信息

Stinco Giuseppe, Favot Francesca, Scott Cathryn Anne, Patrone Pasquale

机构信息

Institute of Dermatology, Department of Clinical and Experimental Pathology and Medicine, University of Udine School of Medicine, Udine, Italy.

出版信息

Int J Dermatol. 2007 Dec;46(12):1267-70. doi: 10.1111/j.1365-4632.2007.03422.x.

Abstract

BACKGROUND

Pigmentatio maculosa eruptiva idiopathica is a rare pediatric disease characterized by asymptomatic, brownish macules involving the neck and trunk with no preceding inflammatory process or history of drug exposure.

METHODS

A 9-year-old girl presented with brown-gray, nonconfluent, asymptomatic macules on the trunk, neck, and limbs, ranging from 5 to 30 mm in diameter. The macules appeared suddenly with no lesions preceding their occurrence. Histopathologic examination showed basal cell layer hyperpigmentation, and abundant melanophages with a mild perivascular lymphohistiocytic infiltrate in the papillary dermis.

RESULTS

The lesions disappeared spontaneously 1.5 years later with no therapy. No relapse occurred.

CONCLUSION

Pigmentatio maculosa eruptiva idiopathica must be differentiated from other skin disorders with hyperpigmentation in pediatric practice in order to avoid unnecessary treatment, as spontaneous resolution is expected. Following a literature review, we underline the importance of spontaneous regression as an additional clinical feature for this disease.

摘要

背景

特发性斑疹性色素沉着病是一种罕见的儿科疾病,其特征为颈部和躯干出现无症状的褐色斑疹,无前驱炎症过程或药物接触史。

方法

一名9岁女孩躯干、颈部和四肢出现棕灰色、不融合的无症状斑疹,直径5至30毫米。斑疹突然出现,出现前无皮损。组织病理学检查显示基底细胞层色素沉着,真皮乳头层有大量噬黑素细胞及轻度血管周围淋巴细胞和组织细胞浸润。

结果

1.5年后未经治疗皮损自行消退,未复发。

结论

在儿科临床实践中,特发性斑疹性色素沉着病必须与其他色素沉着性皮肤病相鉴别,以免进行不必要的治疗,因为预期会自行消退。文献复习后,我们强调自行消退作为该疾病的一项附加临床特征的重要性。

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