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首页> 外文期刊>Indian Dermatology Online Journal >Nonfamilial acrokeratosis verruciformis of Hopf
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Nonfamilial acrokeratosis verruciformis of Hopf

机译:霍普夫氏非家族性角化病

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摘要

Acrokeratosis verruciformis (AKV) of Hopf is an autosomal dominant genodermatosis with unknown etiology. It is characterized by multiple flat-topped keratotic papules resembling planar warts located mainly on the dorsum of hands and feet. Superficial ablation is the treatment of choice. A 41-year-old female presented with multiple hyperpigmented, hyperkeratotic papules and plaques over flexor aspect of both forearms, extensors of both legs and dorsum of the feet. Histopathology showed changes of AKV. Patient was treated with a combination of topical corticosteroids and cryotherapy with no visible improvement.Keywords: Acrokeratosis, church spires, Darier's disease
机译:Hopf的疣状角化病(AKV)是一种常染色体显性遗传皮肤病,病因不明。它的特征是多个平顶的角化丘疹,类似于平面疣,主要位于手和脚的背部。浅表消融是治疗的选择。一名41岁的女性在前臂,双腿的伸肌和脚背的屈肌方面表现出多个色素沉着,角化过度的丘疹和斑块。组织病理学显示AKV的改变。该患者接受了局部皮质类固醇激素和冷冻疗法的联合治疗,但无明显改善。关键词:肢端角化病,教堂尖顶,Darier病

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