Familial Polyposis Coli / 대한소화기내시경학회지
Korean Journal of Gastrointestinal Endoscopy
;
: 395-399, 1993.
Article
Dans Coréen
| WPRIM
| ID: wpr-47652
ABSTRACT
Familial adenomatous polyposis(FAP) is the most oommon of the polyposis syndromes. It is characterized by multiple colorectal adenoma and a high occurrence rate of associated colonic adenocarcinoma in all untreated cases. FPC is inherited as antosomal dominant trait. During 20 years after diagnosis, adenocarcinoma occurs in more than 50% of patients. Clinically, surgical resection should be advised at the time of diagnosis in almost all cases, and acquainted with the potential risks to their children and advised to seek genetic counselling. we report three cases with familial adenomatous polyposis in family.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Adénocarcinome
/
Adénomes
/
Côlon
/
Polypose adénomateuse colique
/
Diagnostic
Type d'étude:
Etude diagnostique
Limites du sujet:
Enfant
/
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Gastrointestinal Endoscopy
Année:
1993
Type:
Article
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS