Korean Journal of Gastrointestinal Endoscopy 1993;13(2): 395-399.
가족성 다발성 대장용종증 3예 ( Familial Polyposis Coli )
박강서, 박찬권, 박성규, 백상현, 이현상, 정경태, 유석준, 조병석, 최덕례, 최호순 (Kang Seo Park, Chan Kwon Park, Seong Kyw Park, Sang Heyun Paik, Hyun Sang Lee, Kyung Tae Jung, Seok Joon Yoo, Byung Seok Cho, Duck Reii Choi and Ho Soon Choi)
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.
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