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6. LONG-TERM RESULTS OF HEPATIC PORTOENTEROSTOMY FOR BILIARY ATRESIA
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Hepatic Portoenterostomy; Kasai Procedure
Rahul G. Baijal, Nihar V. Patel
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Drainage of the biliary tree in infants with biliary atresia remains an unsolved problem, for more than 90% of such infants have an uncorrectable-type lesion, ie, no extra-hepatic bile duct is available for anastomosis to the intestine. The history of attempts to surgically circumvent this problem has been a most depressing one.
David P. Campbell
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Hepatic calcification in an anicteric patient with biliary atresia after hepatic portoenterostomy
AbstractHepatic calcification was found in an anicteric infant with biliary atresia after hepatic portoenterostomy. When she was 2 years of age, ultrasonography detected an echogenic structure with acoustic shadowing. Computerized tomography located it at the proximal portion of Segment 6 in the right lobe.
A, Matsui +7 more
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Morio Kasai Corrects the Uncorrectable: Hepatic Portoenterostomy for Biliary Atresia
Journal of Pediatric SurgeryOne of the fundamental innovations of pediatric surgery is hepatic portoenterostomy for biliary atresia, widely known as the Kasai procedure for its originator, Morio Kasai (1922-2008), of Sendai, Japan. It was the first effective operation for the "uncorrectable" form of biliary atresia, where death within months from biliary cirrhosis was certain ...
Don K. Nakayama
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Essential fatty acid deficiency after hepatic portoenterostomy for biliary atresia
Gas chromatography was used to determine the fatty acid composition of total lipids extracted from plasma and erythrocytes of five patients who had received an hepatic portoenterostomy for treatment of extrahepatic biliary atresia. Three patients, including one with successful surgery, demonstrated evidence of essential fatty acid deficiency, including
G R, Gourley, P M, Farrell, G B, Odell
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CIPROFLOXACIN FOR CHOLANGITIS AFTER HEPATIC PORTOENTEROSTOMY
HOUWEN, RHJ +2 more
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