The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.
临床理表现及家族史都符合掌蹠表皮松解
角化症的诊断。
The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.
临床理表现及家族史都符合掌蹠表皮松解
角化症的诊断。
Treatment: milium, syringgoma, xanthoma of eyelid, benignpapilloma, sudoriceratosis, facial explosive powder thesaurismosis,helosis, leucoderma, acne rosacea, and encapsulated acne,etc.
9、治疗:栗丘疹、汗管瘤、睑黄瘤、良乳头状瘤、汗管角化症、爆炸
(爆炸粉粒沉着症)、鸡眼、胼底、白癜风、酒渣鼻、包裹
粉刺等。
Dyskeratosis congenita (DKC) is a rare inherited disease characterized by the triad of abnormal skin pigmentation, nail dystrophy, and mucosal leukoplakia.
先天角化不良症(DKC)为一少见之遗传
,
项主要特徵为皮肤色素
常、 指甲生长
常及黏膜白斑症。
This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.
本文报告了一例罕见的遗传掌跖皮肤角化
—遗传
残毁
角化瘤,并与各种掌跖皮肤角化症、断肢症的鉴别进行了讨论。
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