Duebbers, M. (2020). Biliary tract surgery in childhood. Chirurg, 91 (1). S. 23 - 29. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1433-0385

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Abstract

In contrast to gallstones, which are increasingly diagnosed in children and adolescents, congenital or perinatally acquired malformations of the biliary tree are rare entities. The surgical treatment of these diseases frequently represents a technical challenge. For children with biliary atresia Kasai portoenterostomy is a therapeutic option in the first weeks of life. Most affected children, however, require a liver transplantation before they enter adulthood. Segmental dilatations of the bile duct carry the risk of ascending infections and malignant transformation. This requires early resection of the biliary tree and reconstruction with a bilioenteric anastomosis. While laparoscopic cholecystectomy has become the standard approach also for children, the value of minimally invasive procedures for more complex surgical procedures of the biliary tract has not yet been defined.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Duebbers, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-128192
DOI: 10.1007/s00104-019-01058-w
Journal or Publication Title: Chirurg
Volume: 91
Number: 1
Page Range: S. 23 - 29
Date: 2020
Publisher: SPRINGER HEIDELBERG
Place of Publication: HEIDELBERG
ISSN: 1433-0385
Language: German
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
CHOLEDOCHAL CYSTS; KASAI PORTOENTEROSTOMY; HEPATICODUODENOSTOMY; HEPATICOJEJUNOSTOMY; RECONSTRUCTION; COMPLICATIONS; RESECTION; EXCISION; OUTCOMES; CHILDRENMultiple languages
SurgeryMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/12819

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