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Primary sclerosing cholangitis (PSC) and prim


ary biliary cirrhosis (PBC) are destructive cholangitis, is difficult to distinguish the two clinical chronic cholestasis syndrome. Of the two groups on the PSC and PBC patients by clinical, biochemical, immunological, X ray and hepatic histological features compared one by one in order to provide a reasonable diagnosis. Materials and Methods: 60 patients with PSC and PBC were 258 cases of cholestatic liver disease, extending more than 6 months, serum alkaline phosphatase more than 2 times the upper limit of normal, and liver biopsy evidence. Selected by X-PSC proved diffuse extrahepatic bile duct stricture, irregular, expansion or distortion, involving or not involving the intrahepatic bile duct system. PSC patients underwent colonoscopy and multiple biopsy and cholangiography. 49 cases for which endoscopic retrograde cholangiography, and 7 cases for bile duct imaging by 4 patients for intraoperative cholangiography. PBC patients were anti-mitochondrial
DOI: cnki: ISSN :1673-534X .0.2
Snapshot text:
Primary sclerosing cholangitis (PSC) and primary biliary cirrhosis (PBC) are destructive cholangitis, is difficult to distinguish the two clinical chronic cholestasis syndrome. Of the two groups on the PSC and PBC patients by clinical, biochemical, immunological, X ray and hepatic histological features compared one by one in order to provide a reasonable diagnosis. Materials and Methods: 60 patients with PSC and PBC were 258 cases of cholestatic liver disease, extending 6
"International Journal of Digestive Diseases" in 1985 and 04 Add to Favorites Get the latest primary sclerosing cholangitis and biliary cirrhosis compared clinical and pathological features of Cai Hua Abstract: Positive primary sclerosing cholangitis (PSC) and the original Recurrent biliary cirrhosis (PBC) are destructive cholangitis, is difficult to distinguish the two clinical chronic cholestasis syndrome. Of the two groups on the PSC and PBC patients by clinical, biochemical, immunological, X ray and hepatic histological features compared one by one in order to provide a reasonable diagnosis. Materials and Methods: 60 patients with PSC and PBC were 258 cases of cholestatic liver disease, extending more than 6 months, serum alkaline phosphatase more than 2 times the upper limit of normal, and liver biopsy evidence. Selected by X-PSC proved diffuse extrahepatic bile duct stricture, irregular, expansion or distortion, involving or not involving the intrahepatic bile duct system. PSC patients underwent colonoscopy and multiple biopsy and cholangiography. 49 cases for which endoscopic retrograde cholangiography, and 7 cases for bile duct imaging by 4 patients for intraoperative cholangiography. PBC patients were anti-mitochondrial Key words: primary sclerosing cholangitis intraoperative cholangiography biliary anti-mitochondrial antibodies of primary biliary cirrhosis and histological features of the clinical identification of serum alkaline phosphatase drying colonoscopy of keratoconjunctivitis
DOI: CNKI: SUN: GWXH.0.2
Snapshot body: primary sclerosing cholangitis (PSC) and primary biliary cirrhosis (PBC) are destructive cholangitis, is difficult to distinguish the two clinical chronic cholestasis syndrome. Of the two groups on the PSC and PBC patients by clinical, biochemical, immunological, X ray and hepatic histological features compared one by one in order to provide a reasonable diagnosis. Materials and Methods: 60 patients with PSC and PBC were 258 cases of cholestatic liver disease, extending full text of more similar 6 full text PDF format document format text CAJ
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