Familial Polyposis Coli / 대한소화기내시경학회지
Korean Journal of Gastrointestinal Endoscopy
;
: 395-399, 1993.
Artículo
en Coreano
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Adenocarcinoma
/
Adenoma
/
Colon
/
Poliposis Adenomatosa del Colon
/
Diagnóstico
Tipo de estudio:
Estudio diagnóstico
Límite:
Niño
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Gastrointestinal Endoscopy
Año:
1993
Tipo del documento:
Artículo
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