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、良乳头状瘤、汗管角化、爆炸伤异物（爆炸粉粒）、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（DKC）为之遗传疾病，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.

本文报告了例罕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、睑黄、良乳、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角化病—遗传残毁角化,并与各种掌跖皮角化症、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、炸伤异物（炸粉粒沉着）、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.

先天角不良（DKC）为一少见之遗传疾病，三项徵为皮肤色素异常、 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病—遗传残毁角瘤,并与各种掌跖皮肤角、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、良瘤、汗管角化症、爆炸伤物（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、爆伤异物（爆沉着症）、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）为一少见疾病，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掌跖皮肤角化病—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、汗管瘤、睑黄瘤、良乳头状瘤、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病—遗传残毁瘤,并与各种掌跖皮症、断肢症的鉴别进行了讨论。