KMID : 0371319920430010137
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Journal of the Korean Surgical Society 1992 Volume.43 No. 1 p.137 ~ p.145
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Report of One Case of Malignant Familial Polyposis Which was Recurred Postoperative Remmant Rectum
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Abstract
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Familial polyposis which is characterized by the appearance, early in life, of large numbers of adenomatous polyps of the colon and rectum is a rare inheritary disease which is transmitted as a Mendelian dominant, non-sex linked trait. The polyps
usually appear at puberty and cause bleeding from the rectum, diarrhea, tenesmus or less commonly intestinal obstruction. The most serious complication is malignant change in the polyps if not treated. Most of untreated patients die before the
age
of 50
from carcinoma of the colon. Therefore, early recognition and management of this disease is warranted. Treatment consists of total colectomy and permenant ileostomy or ileoanal anastomosis with removal of rectal mucosa.
We experienced one case of malignant familial polyposis on 34 year old male patient which was recurred postoperative remmant rectum and report with review of literatures.
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KEYWORD
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