Síndrome de Gardner

Three patients, sisters of e. 12 and 14 years of age with a diagnosis of Gardner's Syndrome are reported The family history indicated that their mather died of a carcinoma of the intestine at "the age of 30. This Syndrome, which is of dominant autosomic interi tance, can be seen in aur cit...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: de Hidalgo, Perla K., Aimar de Irazuzta, Vilma, Tramunt, Bibiana
Formato: Artículo revista
Lenguaje:Español
Publicado: Facultad de Odontología 2018
Materias:
Gardner Syndrome
Case Studies
Síndrome de Gardner
Estudios de Casos
Acceso en línea:https://revistas.unc.edu.ar/index.php/RevFacOdonto/article/view/20684
Aporte de:
Revista de la Facultad de Odontología de Universidad Nacional de Córdoba
id I10-R335-article-20684
record_format ojs
spelling I10-R335-article-206842019-10-22T13:40:45Z Síndrome de Gardner Síndrome de Gardner de Hidalgo, Perla K. Aimar de Irazuzta, Vilma Tramunt, Bibiana Gardner Syndrome Case Studies Síndrome de Gardner Estudios de Casos Three patients, sisters of e. 12 and 14 years of age with a diagnosis of Gardner's Syndrome are reported The family history indicated that their mather died of a carcinoma of the intestine at "the age of 30. This Syndrome, which is of dominant autosomic interi tance, can be seen in aur city. with EO heterogeneous hereditary features. Oentists must know the oral cavity characteristics of this disease [odontomas. cementomas, cysts, supernumerary teeth) that accompany ga~trie. intestinal, skeletal and tissular disturbances an of other organs [polyps, osteomas, cysts. adenomas), being intestinal poliposis of the colon the most important .feat~re that becbmes an "Adenocarcinoma", in the third ald fourth decade in a 100% of the cases. Its incidence in our city is real. The proper diagnosis is made when the clinical study is completed andthe dentist may be the first ene to watch this syndrome' s feature in the oral cavity. A proper medica! diagnosis would allow a preventive procedure and a patient's control until the "total surgery of the colon". which ia the appropiate therapeutic procedure. is achieved; although there are controversias as regards the time to be carried out. Se presentan tres pacientes de sexo femenino, hermanas. de 8, 12 y 14 años de edad con diagnóstico de Síndrome de Gardner, Su rasgo heredita río familiar provenía de su madre fallecida a los 30 años de edad de Fibromatosis retroperitoneal. En nuestro medio, con características hereditarias tan heterogéneas. Puede manifestarse este Síndrome que es hereditário y utosómico domina~te. El Odontólogo debe conocer las manifestaciones bucales de esta enfermedad [odontomas. cementomas, quistes, dientes supernumerarios) que a7compañan a trastornos gastrointestinales, esqueléticos, tisulares y de otros órganos [pólipos, osteomas, quistes, adenomas): siendo el rasgo más importante la "poliposis colónica" que evoluciona a "Adenocarcinoma" entre la tercera y cuarta década en un 100% de los casos. Creemos que la posibilidad de su incidencia en nuestro medio es una realidad. El diagnóstico correcto se realiza al completar el estudio médico-sistémico y, el odontólogo puede ser el primer observador de las manifest~cienes de este Síndrome a nivel de la cavidad bucal. El lograr un correcto diagnóstico médico. permitiría una conducta pr~ ventiva expectante y de control de estos pacientes, hasta llegar a la "colectomía-total" que es el procedimiento terapéutico adecuado, aunque existen controversias en cuanto al momento en que ésta debe efectuarse Facultad de Odontología 2018-07-27 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion application/pdf https://revistas.unc.edu.ar/index.php/RevFacOdonto/article/view/20684 Revista de la Facultad de Odontología; Vol. 17. Enero - Diciembre (1989); 31-41 2545-7594 0325-1071 spa https://revistas.unc.edu.ar/index.php/RevFacOdonto/article/view/20684/27694
institution Universidad Nacional de Córdoba
institution_str I-10
repository_str R-335
container_title_str Revista de la Facultad de Odontología
language Español
format Artículo revista
topic Gardner Syndrome
Case Studies
Síndrome de Gardner
Estudios de Casos
spellingShingle Gardner Syndrome
Case Studies
Síndrome de Gardner
Estudios de Casos
de Hidalgo, Perla K.
Aimar de Irazuzta, Vilma
Tramunt, Bibiana
Síndrome de Gardner
topic_facet Gardner Syndrome
Case Studies
Síndrome de Gardner
Estudios de Casos
author de Hidalgo, Perla K.
Aimar de Irazuzta, Vilma
Tramunt, Bibiana
author_facet de Hidalgo, Perla K.
Aimar de Irazuzta, Vilma
Tramunt, Bibiana
author_sort de Hidalgo, Perla K.
title Síndrome de Gardner
title_short Síndrome de Gardner
title_full Síndrome de Gardner
title_fullStr Síndrome de Gardner
title_full_unstemmed Síndrome de Gardner
title_sort síndrome de gardner
description Three patients, sisters of e. 12 and 14 years of age with a diagnosis of Gardner's Syndrome are reported The family history indicated that their mather died of a carcinoma of the intestine at "the age of 30. This Syndrome, which is of dominant autosomic interi tance, can be seen in aur city. with EO heterogeneous hereditary features. Oentists must know the oral cavity characteristics of this disease [odontomas. cementomas, cysts, supernumerary teeth) that accompany ga~trie. intestinal, skeletal and tissular disturbances an of other organs [polyps, osteomas, cysts. adenomas), being intestinal poliposis of the colon the most important .feat~re that becbmes an "Adenocarcinoma", in the third ald fourth decade in a 100% of the cases. Its incidence in our city is real. The proper diagnosis is made when the clinical study is completed andthe dentist may be the first ene to watch this syndrome' s feature in the oral cavity. A proper medica! diagnosis would allow a preventive procedure and a patient's control until the "total surgery of the colon". which ia the appropiate therapeutic procedure. is achieved; although there are controversias as regards the time to be carried out.
publisher Facultad de Odontología
publishDate 2018
url https://revistas.unc.edu.ar/index.php/RevFacOdonto/article/view/20684
work_keys_str_mv AT dehidalgoperlak sindromedegardner
AT aimardeirazuztavilma sindromedegardner
AT tramuntbibiana sindromedegardner
first_indexed 2024-09-03T21:15:13Z
last_indexed 2024-09-03T21:15:13Z
_version_ 1809211051810488320

Ejemplares similares