Biomaterial Database

Congenital biliary dilatation appearing 3 years after the correction of duodenal atresia with pancreaticobiliary maljunction. 2020

Satoshi Yokoyama, and Tatsuo Nakaoka

Department of, Pediatric Surgery, Japanese Red Cross Society, Wakayama Medical Center, Wakayama, Japan.

UI	MeSH Term	Description	Entries
D007409	Intestinal Atresia	Congenital obliteration of the lumen of the intestine, with the ILEUM involved in 50% of the cases and the JEJUNUM and DUODENUM following in frequency. It is the most frequent cause of INTESTINAL OBSTRUCTION in NEWBORNS. (From Stedman, 25th ed)	Atresia, Intestinal,Apple Peel Small Bowel Syndrome,Apple Peel Syndrome,Apple-Peel Intestinal Atresia,Congenital Intestinal Atresia,Familial Apple Peel Jejunal Atresia,Jejunal Atresia,Apple Peel Intestinal Atresia,Apple Peel Syndromes,Apple-Peel Intestinal Atresias,Atresia, Apple-Peel Intestinal,Atresia, Congenital Intestinal,Atresia, Jejunal,Atresias, Apple-Peel Intestinal,Atresias, Congenital Intestinal,Congenital Intestinal Atresias,Intestinal Atresia, Apple-Peel,Intestinal Atresia, Congenital,Intestinal Atresias, Apple-Peel,Intestinal Atresias, Congenital
D004108	Dilatation, Pathologic	The condition of an anatomical structure's being dilated beyond normal dimensions.	Ectasia,Dilatation, Pathological,Dilatations, Pathologic,Dilatations, Pathological,Pathologic Dilatation,Pathologic Dilatations,Pathological Dilatation,Pathological Dilatations
D004380	Duodenal Obstruction	Hindrance of the passage of luminal contents in the DUODENUM. Duodenal obstruction can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is associated with diminished or stopped flow of luminal contents. Strangulating obstruction is associated with impaired blood flow to the duodenum in addition to obstructed flow of luminal contents.	Duodenal Obstructions,Obstruction, Duodenal,Obstructions, Duodenal
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000080222	Pancreaticobiliary Maljunction	A group of anatomical variations in which the COMMON BILE DUCT and MAIN PANCREATIC DUCT are joined outside the duodenal wall often with abnormally long common channel rather than at the SPHINCTER OF ODDI.	Anomalous Pancreaticobiliary Ductal Union,Anomalous Pancreaticobiliary Junction,Anomalous Pancreaticobiliary Junctions,Junction, Anomalous Pancreaticobiliary,Maljunction, Pancreaticobiliary,Pancreaticobiliary Junction, Anomalous,Pancreaticobiliary Maljunctions
D015529	Choledochal Cyst	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.	Choledochal Cyst, Type I,Common Bile Duct Cyst,Congenital Biliary Dilatation,Congenital Choledochal Cyst,Bile Duct Cysts,Choledochal Cyst, Diverticulum,Choledochal Cyst, Type II,Choledochal Cyst, Type III,Choledochal Cyst, Type IV,Choledochal Cyst, Type V,Choledochal Diverticulum,Choledochocele,Cyst, Common Bile Duct,Cysts, Common Bile Duct,Intrahepatic Choledochal Cyst,Multiple Choledochal Cysts,Bile Duct Cyst,Biliary Dilatation, Congenital,Choledochal Cyst, Congenital,Choledochal Cyst, Intrahepatic,Choledochal Cyst, Multiple,Choledochal Cysts,Choledochal Cysts, Diverticulum,Choledochal Diverticulums,Choledochoceles,Congenital Biliary Dilatations,Congenital Choledochal Cysts,Cyst, Bile Duct,Cyst, Choledochal,Cyst, Congenital Choledochal,Cyst, Intrahepatic Choledochal,Cyst, Multiple Choledochal,Dilatation, Congenital Biliary,Diverticulum Choledochal Cyst,Diverticulum Choledochal Cysts,Diverticulum, Choledochal,Duct Cyst, Bile,Intrahepatic Choledochal Cysts,Multiple Choledochal Cyst