一名 11 岁男孩出现特发性爆发性黄斑色素沉着

Q4 Medicine
Pavel N. Trofimov, Khairutdinov R. Vladislav, Maria A. Fedotova, Irena E. Belousova
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引用次数: 0

摘要

一例儿童特发性爆发性黄斑色素沉着显示了一种病因不明的皮肤色素沉着变异。我们描述了一名 11 岁男孩的病例,他的躯干和四肢出现浅褐色斑点,其背景是正常皮肤,没有确定的诱发因素。经检查发现,该病是在一年内发病的。起初,皮疹局限于肘部皱褶和腋窝部位,后来皮疹扩散到躯干、颈部和四肢。皮疹基底未见炎症变化。对患者进行了检查,以确定是否存在可能导致皮肤表现的疾病,并进行了组织学检查以核实诊断。由于现有的文献资料表明这种病症会自行消退,而且现有的皮肤病治疗方案效果不佳,因此确诊为特发性爆发性黄斑色素沉着症后,患者的治疗选择了观望态度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of idiopathic eruptive macular pigmentation in an 11-year-old boy
A case of idiopathic eruptive macular pigmentation in a child demonstrates a variant of skin hyperpigmentation of uncertain etiology. We described an 11-year-old boy with light brown spots in the torso and limbs that developed against the background of normal skin without an established provoking factor. On examination, it was found that the disease had developed within one year. Initially, the process was localized to the elbow folds and axillary areas, but later the rash spread to the trunk, neck and extremities. No inflammatory changes were observed at the base of the rash elements. The patient was examined for the presence of diseases that could underlie the skin manifestations, and histological examination was performed to verify the diagnosis. The established diagnosis of idiopathic eruptive macular pigmentation made it possible to choose a wait-and-see approach in treating the patient, due to the available literature data on the self-resolution of this pathology and ineffectiveness of the available dermatosis treatment options.
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
40
审稿时长
8 weeks
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