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：、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、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、、睑黄、良乳头状、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）一少见之遗传疾病，三项主要特徵色素异常、 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角化病—遗传残毁角化,并与各种掌跖角化症、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.

临床理家族史都符合掌蹠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）为一少见之疾，三项主要特徵为皮肤色素异常、 指甲生长异常黏膜白斑症。

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—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.

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、管瘤、睑黄瘤、良乳头状瘤、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。