The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病理表现及家族史都符合掌蹠表皮松解症的诊断。

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、睑黄、良乳头状、汗管症、爆炸伤异物（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.

先天不良症（DKC）为一少见之遗传疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

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.

本文报告了一罕见的遗传掌跖皮肤病—遗传残毁,并与各种掌跖皮肤症、断肢症的鉴别进行了讨论。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病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、爆炸伤异物（爆炸着症）、鸡眼、胼底、白癜风、酒渣鼻、包裹刺等。

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）为一少传疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

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.

本文报告了一例罕的传掌跖皮肤角化病—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。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病理表现及家族史都符合掌蹠表皮松解化症的诊断。

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、汗管化症、爆炸伤异物（爆炸粉粒沉着症）、鸡眼、胼底、白、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.

先化不良症（DKC）为一少见之遗传疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

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化病—遗传残毁化瘤,并与各种掌跖皮肤化症、断肢症的鉴别进行了讨论。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病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、爆炸伤异物（爆炸粒沉着症）、鸡眼、胼底、白癜风、酒渣、。

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）为一少见之遗传疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

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病—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。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病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、爆炸伤异物（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）为一少见之遗传疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

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病—遗传残毁角化瘤,种掌跖皮肤角化症、断肢症的鉴别进行了讨论。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病理表现及家族史都符合掌蹠表皮松解角化的诊断。

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、乳头状瘤、汗管角化、爆炸伤异物（爆炸粉粒沉着）、、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（DKC）一少见之遗传疾病，三项主要特徵皮肤色素异常、 指甲生长异常及黏膜白斑。

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病—遗传残毁角化瘤,并与各种掌跖皮肤角化、断肢的鉴别进行了讨论。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病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、爆炸伤异物（爆炸粉粒沉着症）、鸡眼、胼底、白癜风、酒、裹粉。

Dyskeratosis congenita (DKC) is a rare inherited disease characterized by the triad of abnormal skin pigmentation, nail dystrophy, and mucosal leukoplakia.

天角化不良症（DKC）为一少见之遗传疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

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病—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。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病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、爆炸伤异物（爆炸粒沉着症）、鸡眼、胼底、白癜风、酒渣、。

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）为一少见之遗传疾病，三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。

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病—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。

The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.

临床病理现及家族史都符合掌松解角化症诊断。

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、爆炸伤异物（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）为一少见之疾病，三项主要特徵为肤色素异常、 指甲生长异常及黏膜白斑症。

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掌跖肤角化病—残毁角化瘤,并与各种掌跖肤角化症、断肢症鉴别进行了讨论。