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The importance of the dentist in the diagnosis of Cowden syndrome: case report
Author(s) -
Camila Feier Viegas,
Tulio de Lucena Pires,
Paulo Tadeu de Souza Figueiredo,
André Ferreira Leite,
Clemes Alves Mesquita
Publication year - 2016
Publication title -
brazilian dental science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.153
H-Index - 6
ISSN - 2178-6011
DOI - 10.14295/bds.2016.v19i3.1262
Subject(s) - cowden syndrome , medicine , dermatology , hamartoma , thyroid , pediatrics , pathology , pten , apoptosis , biochemistry , chemistry , pi3k/akt/mtor pathway
Cowden Syndrome is an autosomal dominant disorder characterized by the development of several hamartomas in a variety of tissues, including the skin, gastrointestinal tract, adipose tissue, and bone and connective tissues. This syndrome is associated with a high risk of developing malignancies, especially breast, thyroid and endometrium cancers. This report presents a case of a 53-year-old patient who sought assistance at the Dentistry Department of the University Hospital of Brasilia (HUB) to receive basic dental treatment. The current and past medical history and oral and facial manifestations led to the diagnosis of Cowden syndrome . This case report aims to highlight the importance of a dental surgeon in the diagnosis of this syndrome, based on the observation of oral manifestations and medical history. Keywords Cowden Syndrome; Multiple Hamartoma Syndrome.

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