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
收藏
页码：292 / 293
页数：2
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