KMID : 0359019930130020395
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Korean Journal of Gastrointestinal Endoscopy 1993 Volume.13 No. 2 p.395 ~ p.400
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Familial Polyposis Coli
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Abstract
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Familial adenomatous polyposis(FAP) is the most common of the polyposis syndromes. It is characterized by multiple colorectal adenoma and a high occurrence rate of associated colonic adenocarcinoma in all untreated cases.
EPC 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.
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KEYWORD
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