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色素异常性皮肤淀粉样变1例 被引量:1

A Case of Amyloidosis Cutis Dyschromica
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摘要 患儿女,6岁。全身皮肤泛发色素减退斑2年。全身皮肤弥漫性分布粟粒至绿豆大色素减退斑,以腰背部和双小腿伸侧为著,手、足均无受累,触诊有充实、小结节状感觉。皮损组织病理示:表皮角化过度,真皮乳头层见块状嗜酸性样物质沉积,刚果红染色(+)。诊断:色素异常性皮肤淀粉样变。 A 6-year-old girl was referred to our out-patient elinie with /he chief complaint of hypopigmented macules o- ver her whole body for 2 years. Clinical examination showed diffuse, millet-tu green bean-sized, hypopig- mented maeules over the whole body except hands and feet. Palpation felt solid nodules. Histopathologic examination showed epidermal hyperkeratosis and deposition eosinophilic substance in the dermal papillary lay- er. Congu red staining was positive. Diagnosis was dyschrumiea culls amyloidosis.
作者 杨婷 蒋献
出处 《中国皮肤性病学杂志》 CAS CSCD 北大核心 2015年第6期617-618,共2页 The Chinese Journal of Dermatovenereology
关键词 皮肤淀粉样变 色素异常 Amyloidosis Cutis Dyschromica Dyschromica
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参考文献9

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