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考登综合征的口腔表现。4例报告。

Oral manifestations in Cowden's syndrome. Report of four cases.

作者信息

Swart J G, Lekkas C, Allard R H

出版信息

Oral Surg Oral Med Oral Pathol. 1985 Mar;59(3):264-8. doi: 10.1016/0030-4220(85)90164-1.

Abstract

Cowden's syndrome or multiple hamartoma and neoplasia syndrome is a hereditary disorder combining multiple hamartomas of many organs. These hamartomas are derived from ectodermal, mesodermal, and endodermal tissues and may undergo spontaneous malignant changes. Small papular cutaneous lesions and papillomatous outgrowth and papular lesions of the oral mucosa are the most predominant features of the syndrome. Since the orocutaneous lesions often precede the associated malignant degenerations, they may serve as a diagnostic signal for the probably developing neoplasia in other organs. The presence of extensive papillomatous and papular lesions in the oral mucosa combined with skin lesions should therefore alert the clinician to suspect the presence of Cowden's syndrome, the early diagnosis of which is important in order that the concomitant malignant changes might be discovered at the earliest possible moment. Four cases of Cowden's disease are presented, with emphasis on the oral manifestations of this syndrome.

摘要

考登综合征或多发性错构瘤及肿瘤形成综合征是一种遗传性疾病,合并多个器官的多发性错构瘤。这些错构瘤源自外胚层、中胚层和内胚层组织,可能会发生自发性恶性变化。小丘疹性皮肤损害、乳头状赘生物及口腔黏膜的丘疹性损害是该综合征最主要的特征。由于口皮肤损害常常先于相关的恶性退变出现,它们可能作为其他器官可能发生肿瘤形成的诊断信号。因此,口腔黏膜广泛存在乳头状和丘疹性损害并伴有皮肤损害,应提醒临床医生怀疑考登综合征的存在,早期诊断该病很重要,以便能尽早发现伴随的恶性变化。本文报告4例考登病,重点介绍该综合征的口腔表现。

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