医学
棘皮病
皮肤病科
无症状的
角化过度
头皮
表皮松解性角化过度
角膜溶解
病理
作者
Julie K Sracic,R. S. Krishnan,Janna Nunez‐Gussman,Ida Orengo,Sylvia Hsu
摘要
Hereditary papulotranslucent acrokeratoderma is a rare autosomal-dominant syndrome of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis. Histopathologically, focal hyperkeratosis, hypergranulosis, and acanthosis of the epidermis are seen. We present a case of hereditary papulotranslucent acrokeratoderma in a young adult woman. The literature of this unusual condition is reviewed, and its relationship to acquired papulotranslucent acrokeratoderma is discussed.
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