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Familial Adenomatous Polyposis with Gallbladder Polyps

대한대장항문학회지 1997년 13권 3호 p.535 ~ 540
배진한 ( Bae Jin-Han ) - 삼척의료원 일반외과

황창선 ( Hwang Chang-Sun ) - 삼척의료원 일반외과
최영희 ( Choi Young-Hee ) - 한림대학교 의과대학 병리학교실


Familial adenomatous polyposis(FAP) is an inherited autosomal dominant disorder characterized by the appearance in early life of numerous adenomas of colon and rectum. According to the recent studies, familial polypolis is a disease which produces polypoid lesions not only in the large intestine but also in the stomach duodenum, ileum and jejunum. The natural course of extracolonic lesions is variable, but the colonic polyps are associated with high incidence of cancer. The risk of malignant change is virtually 100% if untreated. The authors report a case of FAP in a 36-year-old-female who
presented colorectal polyposis with multiple adenomas of the gallbladder. A review of literature with emphasis on the association of adenoma of the gallbladder was made.


Familial Adenomatous Polyposis(FAP)
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