نتایج جستجو برای: sclerosing cholangitis

تعداد نتایج: 8177  

2004
Erkan PARLAK Sedef ÖZDAL KURAN Selçuk DİŞİBEYAZ Bahattin ÇİÇEK Dilek OĞUZ Burhan ŞAHİN

Background/Aims: Dominant stricture of an extrahepatic bile duct is responsible for symptoms and an exacerbation of cholestasis in 15-20% of patients with primary sclerosing cholangitis. The aim of this study was to evaluate the efficacy and safety of endoscopic treatment in this selected patient group. Methods: Retrospectively, we evaluated 16 patients who were treated endoscopically due to el...

Journal: :Current Opinion in Gastroenterology 2017

Journal: :Gut 1997
P Kelly S Patchett D McCloskey E Alstead M Farthing P Fairclough

BACKGROUND Primary sclerosing cholangitis develops in 3-10% of patients with ulcerative colitis, and may be associated with an increased cancer risk. Ulcerative colitis is probably less common in people of African origin than in populations of European descent. AIMS AND METHODS To review the records of all patients under regular follow up for ulcerative colitis at St Bartholomew's Hospital (L...

Journal: :Gut 1993
W J Sandborn R H Wiesner W J Tremaine N F Larusso

Thirty five adult patients with precirrhotic primary sclerosing cholangitis were randomly allocated to treatment for at least one year with low dose (4.1 mg/kg/day) cyclosporin or placebo in a double blind trial. Thirty patients had coexisting ulcerative colitis, including three who had previously undergone colectomy and one who discontinued treatment after three months. Of the remaining 26 pat...

2017
Jianchun Xiao Guanqiao Li Gang Yang Congwei Jia Binglu Li

RATIONALE IgG4-related disease is a newly recognized fibroinflammatory disorder, characterized by tumefactive lesions, storiform fibrosis and IgG4-positive plasma cells infiltration. IgG4-related sclerosing cholangitis (IgG4-SC) is the most common extrapancreatic manifestation of IgG4-related disease, but it is frequently associated with autoimmune pancreatitis(AIP). Only few case was reported ...

Journal: :Journal of pediatric gastroenterology and nutrition 2014
Pengyun Wang Haibin Su James Underhill Laura J Blackmore Maria Serena Longhi Tassos Grammatikopoulos Elizabeth Veronica Okokon Edward T Davies Diego Vergani Giorgina Mieli-Vergani Yun Ma

OBJECTIVE Familial clustering of juvenile autoimmune liver disease (AILD), including autoimmune hepatitis and autoimmune sclerosing cholangitis (ASC), is rare, despite a high prevalence of autoimmune disorders in AILD families. METHODS To investigate this discrepancy, we measured autoantibodies diagnostic for AILD, anti-nuclear, anti-smooth muscle, anti-liver kidney microsomal type 1, anti-li...

Journal: :Gut 1998
G V Papatheodoridis M Hamilton P K Mistry B Davidson K Rolles A K Burroughs

BACKGROUND The course of inflammatory bowel disease after liver transplantation has been reported as variable with usually no change or improvement, but there may be an increased risk of early colorectal neoplasms. In many centres steroids are often withdrawn early after transplantation and this may affect inflammatory bowel disease activity. AIMS To evaluate the course of inflammatory bowel ...

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