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弥漫性非表皮松解性掌跖角化病1例 被引量:1

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摘要 1病历摘要 患者女,42岁。闲双侧掌跖角化40余年,于2006年9月来我院就诊。患者自婴儿期起无明显诱凶双手掌出现对称性片状红斑,角化,形状不规则.受累皮肤粗糙增厚,同时累及双足和甲板,指(趾)甲增厚、浑浊,呈灰黄色。皮损逐渐向周同扩展,至青春期时已经累及双手整个掌侧、腕部及于背的大部分,双足跖和足背亦呈弥漫性角化过度,跖部较重,皮损呈对称性,
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2007年第12期783-784,共2页 Journal of Clinical Dermatology
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  • 1STEVENS liP, KELSELL DP, BRYANT SP, et al. Linkage of an American pedigree with palmoplantar keratoderma and malignancy ( palmoplantar ectodermal dysplasia type Ⅲ) to 17q24. Literature survey and proposed updated classification of the keratodermas[J].Arch Dermatol, 1996,132(6) :640-651.

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