SciELO - Scientific Electronic Library Online

 
vol.10 número5Hiperplasia multifocal del epitelio: Reporte de nueve casos índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Artigo

Indicadores

Links relacionados

  • Em processo de indexaçãoCitado por Google
  • Não possue artigos similaresSimilares em SciELO
  • Em processo de indexaçãoSimilares em Google

Compartilhar


Medicina Oral, Patología Oral y Cirugía Bucal (Ed. impresa)

versão impressa ISSN 1698-4447

Resumo

CHIMENOS-KUSTNER, Eduardo; PASCUAL, Montserrat; BLANCO, Ignacio  e  FINESTRES, Fernando. Hereditary familial polyposis and Gardner's syndrome: Contribution of the odonto-stomatology examination in its diagnosis and a case description. Med. oral patol. oral cir. bucal (Ed.impr.) [online]. 2005, vol.10, n.5, pp.402-409. ISSN 1698-4447.

Familial adenomatous polyposis (FAP) and its phenotype variant, Gardner's syndrome, constitute a rare autosomal dominant inherited disorder. They are characterised by the development, generally during the second and third decades of life, of multiple adenomatous polyps in the colon and rectum. These polyps have a high risk of subsequently becoming malignant, which normally occurs in the third and fourth decades of life. The phenotypical features of FAP can be very variable. As well as colorectal polyps, these individuals can present with extra-colonic symptoms, among which are particularly: gastro-duodenal polyps, dermoid and epidermoid cysts, desmoid tumours, congenital hypertrophy of the retinal pigment epithelium, disorders of the maxillary and skeletal bones and dental anomalies. In this paper the most important aspects of this syndrome are reviewed, showing an example based on a well documented clinical case. The importance of odonto-stomatological examinations should be pointed out, among others, as a means of reaching a presumptive diagnosis, whose confirmation is vital to the patient.

Palavras-chave : Hereditary familial polyposis; Gardner's syndrome; osteomas; diagnostic markers.

        · resumo em Espanhol     · texto em Espanhol | Inglês     · Inglês ( pdf ) | Espanhol ( pdf )

 

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons