Cowden syndrome

被引：0

作者：

Cannavo, SP

Lagreca, S

Nucifora, G

Guarneri, B

机构：

[1] GARIBALDI HOSP,DERMATOL SERV,CATANIA,ITALY

[2] SANTO BAMBINO HOSP,DIV HUMAN PATHOL,CATANIA,ITALY

来源：

EUROPEAN JOURNAL OF DERMATOLOGY | 1996年 / 6卷 / 04期

关键词：

D O I：

暂无

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Cowden's disease (CD) is a rare syndrome (little more than 100 cases reported in the literature) [1], inherited as an autosomal dominant trait with an incomplete penetrance and variable expressivity [2] and characterized by multiple hamartomas and neoplasms of ectodermal, mesodermal and endodermal origin, predominantly localized to skin, breast, thyroid gland and gastrointestinal tract. On this subject we describe a case of a patient with oral papillomatosis, acral keratoses, intestinal polyps and goiter.

引用

页码：292 / 293

页数：2

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