Oral manifestations of Cowden’s diseasepresentation of a clinical case
- Rafael Segura Saint Gerons 1
- Alejandro Ceballos Salobreña 2
- Mariano Toro Rojas 3
- José Manuel Gándara Rey 4
- 1 Centro de Salud Peñarroya. Córdoba
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2
Universidad de Granada
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3
Universidad de Córdoba
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4
Universidade de Santiago de Compostela
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ISSN: 1698-6946
Año de publicación: 2006
Volumen: 11
Número: 5
Páginas: 7
Tipo: Artículo
Otras publicaciones en: Medicina oral, patología oral y cirugía bucal. Ed. inglesa
Resumen
Cowden’s disease, or multiple hamartoma syndrome, is an autosomal dominant genodermatosis, characterized by the presence of multiple cutaneous hamartomas, oral fibromas and benign acral keratosis. It affects multiple organs (breast, thyroids, stomach, colon), with the strong possibility of malignant neoplasia developing in these organs. We present a case of this rare syndrome, highlighting the presentation of some clinical characteristics that, in suspected cases, can help to establish an early diagnosis of this disease, this being of great importance given the high frequency of tumors in people with this clinical picture.