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、、良乳头状、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,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蹠表松解角化症的诊断。

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肤角化病—遗传残毁角化瘤,并与各种肤角化症、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角化病—遗传残毁角化瘤,并与各种掌角化症、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.

先天化不良症（DKC）为一少见之遗传疾病，三项主要特徵为色素异常、 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化病—遗传残毁化瘤,并与各种掌跖化症、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皮肤角化病—遗传残毁角化瘤,并与各皮肤角化症、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、伤异（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掌跖皮肤角化病—遗残毁角化瘤,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、汗瘤、睑黄瘤、良乳头状瘤、汗症、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）一少见之遗传疾病，三项主要皮肤色素异常、 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病—遗传残毁瘤,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跖皮肤角化病—遗传残毁角化瘤,并与跖皮肤角化症、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）、鸡、、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（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。

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。