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Choledochal Cyst  

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Tipo

  • mesh:Descriptor

Definición

  • A congenital anatomic malformation of a bile duct, including cystic dilatation of the extrahepatic bile duct or the large intrahepatic bile duct. Classification is based on the site and type of dilatation. Type I is most common. Characterized by the choledochocele dilatation of the distal portion of the COMMON BILE DUCT in the DUODENUM where the pancreatic duct (PANCREATIC DUCTS) enters. Concomitant PANCREATICOBILIARY MALJUNCTION and local dilatation of the extrahepatic bile duct. Characterized by the fusiform or saccular dilatation of the COMMON BILE DUCT. Characterized by the presence of a singular or multiple intrahepatic cysts. Characterized by the diverticulum arising from the extrahepatic biliary tree. Characterized by the presence of multiple extrahepatic and intrahepatic cysts.

Conceptos específicos

Etiquetas alternativas

  • Bile Duct Cysts
  • Choledochocele
  • Congenital Choledochal Cyst

En otras lenguas

  • francés

  • Dilatation kystique congénitale du cholédoque
  • DKC (Dilatation Kystique du Cholédoque)
  • Kyste cholédocien
  • Kyste congénital du cholédoque
  • Kyste du canal cholédoque
  • Kystes congénitaux du cholédoque

URI

http://data.loterre.fr/ark:/67375/JVR-KR427TBT-X

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