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掌跖角化病及伴有唇部皮肤角的口腔白斑病。

Palmoplantar keratoderma and oral leucoplakia with cutaneous horn of the lips.

作者信息

Baykal C, Savci N, Kavak A, Kurul S

机构信息

Department of Dermatology and Oncology Institute, Medical School, Istanbul University, 34390 Istanbul, Turkey.

出版信息

Br J Dermatol. 2002 Apr;146(4):680-3. doi: 10.1046/j.1365-2133.2002.04595.x.

Abstract

The inherited palmoplantar keratodermas (PPK) may be associated with a wide variety of other ectodermal abnormalities. The coexistence of PPK and leucoplakia may indicate the increased risk of oesophageal carcinoma in adult life. Cutaneous horn may develop over benign, precancerous, as well as malignant lesions, and frequently may be associated with actinic keratoses and Bowen's disease. On the other hand, the relationship of cutaneous horn and leucoplakia has been the subject of only a single case report. We present a case of PPK and diffuse oral leucokeratosis associated with relapsing cutaneous horn of the lips.

摘要

遗传性掌跖角化病(PPK)可能与多种其他外胚层异常相关。PPK与黏膜白斑并存可能表明成年后患食管癌的风险增加。皮肤角可发生于良性、癌前以及恶性病变之上,且常与光化性角化病和鲍温病相关。另一方面,皮肤角与黏膜白斑的关系仅有一篇病例报告。我们报告一例伴有复发性唇部皮肤角的PPK和弥漫性口腔黏膜白斑病。

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