Surgical significance of persistent cholecystohepatic ducts. 1989

V N Ortiz, and E Vidal, and J S Padilla

Anatomical variations of the biliary tract occur frequently enough so as to worry the general surgeon dealing with this problem. Generally speaking, these anatomical variations are not identified prior to surgery. Anomalous drainage of the common hepatic duct into the gall bladder was identified while performing a cholecystectomy. The common bile duct proximal to the cystic duct was atretic. The problem described above was successfully managed by hepatico-jejunostomy.

UI MeSH Term Description Entries
D007583 Jejunum The middle portion of the SMALL INTESTINE, between DUODENUM and ILEUM. It represents about 2/5 of the remaining portion of the small intestine below duodenum. Jejunums
D002763 Cholecystectomy Surgical removal of the GALLBLADDER. Cholecystectomies
D002769 Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). Gallstone Disease,Cholelithiases,Gallstone Diseases
D003135 Common Bile Duct The largest bile duct. It is formed by the junction of the CYSTIC DUCT and the COMMON HEPATIC DUCT. Choledochus,Bile Duct, Common,Common Bile Ducts,Duct, Common Bile
D005260 Female Females
D006500 Hepatic Duct, Common Predominantly extrahepatic bile duct which is formed by the junction of the right and left hepatic ducts, which are predominantly intrahepatic, and, in turn, joins the cystic duct to form the common bile duct. Common Hepatic Duct,Hepatic Duct,Common Hepatic Ducts,Duct, Common Hepatic,Duct, Hepatic,Ducts, Common Hepatic,Ducts, Hepatic,Hepatic Ducts,Hepatic Ducts, Common
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000755 Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. Hemoglobin S Disease,HbS Disease,Sickle Cell Anemia,Sickle Cell Disease,Sickle Cell Disorders,Sickling Disorder Due to Hemoglobin S,Anemias, Sickle Cell,Cell Disease, Sickle,Cell Diseases, Sickle,Cell Disorder, Sickle,Cell Disorders, Sickle,Disease, Hemoglobin S,Hemoglobin S Diseases,Sickle Cell Anemias,Sickle Cell Diseases,Sickle Cell Disorder

Related Publications

V N Ortiz, and E Vidal, and J S Padilla
August 1980, Archives of surgery (Chicago, Ill. : 1960),
V N Ortiz, and E Vidal, and J S Padilla
January 1996, Ryoikibetsu shokogun shirizu,
V N Ortiz, and E Vidal, and J S Padilla
April 1964, Annals of surgery,
V N Ortiz, and E Vidal, and J S Padilla
February 1984, Ugeskrift for laeger,
V N Ortiz, and E Vidal, and J S Padilla
August 1945, Annals of surgery,
V N Ortiz, and E Vidal, and J S Padilla
July 1962, American journal of surgery,
V N Ortiz, and E Vidal, and J S Padilla
May 1978, American journal of surgery,
V N Ortiz, and E Vidal, and J S Padilla
November 1979, Journal of the Royal College of Surgeons of Edinburgh,
V N Ortiz, and E Vidal, and J S Padilla
January 1975, The British journal of clinical practice,
V N Ortiz, and E Vidal, and J S Padilla
August 1950, Annals of surgery,
Copied contents to your clipboard!