Mørk C, Gabrielsen T O
Hudavdelingen, Rikshospitalet, Oslo.
Tidsskr Nor Laegeforen. 1991 Aug 20;111(19):2432-4.
We describe a patient with Cowden's disease, a rare genodermatosis characterized by multiple hamartomas and neoplasms of ectodermal, mesodermal and endodermal origin. The most characteristic findings are mucocutaneous lesions, including facial trichilemmomas, oral papillomatosis, and acral and palmoplantar keratoses. It is important to recognize these markers because of the high incidence of internal malignancy, the most common being breast cancer. Multiple extracutaneous hamartomas are described as being predominantly localized to breasts, thyroid gland, and gastrointestinal tract. Associated anomalies in multiple organs are frequently found.
我们描述了一名患有考登病的患者,考登病是一种罕见的遗传性皮肤病,其特征为外胚层、中胚层和内胚层来源的多发性错构瘤和肿瘤。最具特征性的表现是皮肤黏膜病变,包括面部毛发上皮瘤、口腔乳头瘤病以及手足角化病。认识到这些标志物很重要,因为内部恶性肿瘤的发病率很高,最常见的是乳腺癌。多发性皮肤外错构瘤主要见于乳房、甲状腺和胃肠道。多个器官常伴有异常。