نتایج جستجو برای: familial polyps

تعداد نتایج: 66728  

Journal: :Oncology 1991
D G Jagelman

Familial adenomatous polyposis (FAP) is a genetic disease created by an abnormality of chromosome number five resulting in a generalized cellular growth disorder. The growth abnormality created by the genetic defect dictates the development of benign and malignant lesions in different organs of the body. Even the term familial adenomatous polyposis does not fully describe the defect because les...

2014

Gardner syndrome (GS) is a group of diseases manifested as familial adenomatous polyposis accompanied by characteristic jaw lesions. The documented prevalence of Gardner syndrome varies from 1: 8,300 to 1: 16,000 live births in varying literatures [1]. The syndrome associated intestinal polyps have a 100% risk of malignant transformation [2]. Early identification and surgical intervention of th...

Journal: :Gut 1979
H Itoh K Ohsato T Yao M Iida H Watanabe

Two sisters with Turcot's syndrome, in which malignant cerebral neoplasms are associated with colonic polyposis, are presented. Cases reported in the literature, including some familial cases, have also been analysed. In familial cases, sex was unrelated to the occurrence of this disease and it was found only among siblings of the same parents and not in other members of the family. There was c...

2008
S. A. R. COOKE

the inherited polyposis syndromes and colorectal carcinoma. Four patients are reported, to illustrate the wide spectrum of colonic polyps which may occur in multiple form in adults. Included are unusual cases of metaplastic and-juvenile polyposis. The subject is reviewed, and the need for accurate histological diagnosis is stressed. The possibility that the difference between familial adenomato...

Journal: :Cancer research 1997
D J Marsh S Roth K L Lunetta A Hemminki P L Dahia P Sistonen Z Zheng S Caron N J van Orsouw W F Bodmer S E Cottrell M G Dunlop D Eccles S V Hodgson H Järvinen I Kellokumpu D Markie K Neale R Phillips P Rozen S Syngal J Vijg I P Tomlinson L A Aaltonen C Eng

Juvenile polyposis syndrome (JPS; MIM 174900) is an autosomal dominant condition with incomplete penetrance characterized by hamartomatous polyps of the gastrointestinal tract and a risk of gastrointestinal cancer. Gastrointestinal hamartomatous polyps are also present in Cowden syndrome (CS; MIM 158350) and Bannayan-Zonana syndrome (BZS; also called Ruvalcaba-Myhre-Smith syndrome; MIM 153480)....

Journal: :Archives of surgery 2002
Juan M Sarmiento Geoffrey B Thompson David M Nagorney John H Donohue Michael B Farnell

HYPOTHESIS Pancreas-sparing duodenectomy (PSD) is a safe and effective operative procedure for patients with nonmalignant duodenal polyps. DESIGN Retrospective analysis of outcomes in patients undergoing PSD. SETTING A tertiary referral center. PATIENTS All patients undergoing PSD at the Mayo Clinic, Rochester, Minn. Indications were the presence of numerous duodenal polyps or large, soli...

Journal: :Journal of the Canadian Association of Gastroenterology 2020

Journal: :Facta Universitatis, Series: Medicine and Biology 2018

Journal: :Gut 2002
W-M Wong N Mandir R A Goodlad B C Y Wong S B Garcia S-K Lam N A Wright

BACKGROUND The histogenesis of human colorectal hyperplastic polyps and colorectal adenomas is poorly understood even now. METHOD Human colorectal adenomas, hyperplastic polyps, and normal colorectal mucosae (patients with familial adenomatous polyposis and hereditary non-polyposis colorectal carcinoma were excluded) were obtained during colonoscopy and microdissected into individual crypts. ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید