extrahepatic biliary obstruction - ορισμός. Τι είναι το extrahepatic biliary obstruction
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Τι (ποιος) είναι extrahepatic biliary obstruction - ορισμός

CONGENITAL DISORDER OF DIGESTIVE SYSTEM INVESTIGATION OF CHOICE OF THE DISEASE IS MRCP
Atresia of bile ducts; Billiary atresia; Biliary atresia, extrahepatic; Extrahepatic biliary atresia

Biliary tract         
  • Union of common bile duct and pancreatic duct terminating at duodenum (small intestine).
ORGAN SYSTEM COMPRISING THE LIVER, GALL BLADDER AND BILE DUCTS
Biliary tract (anatomy); Bilary tract; Hepatobiliary; Hepatobiliary System; Biliary system; Biliary tree; Hepatobiliary tree; Gallways; Biliary tract obstruction; Hepatobiliary systems; Hepatobiliary trees; Hepatobiliary system
The biliary tract, (biliary tree or biliary system) refers to the liver, gall bladder and bile ducts, and how they work together to make, store and secrete bile. Bile consists of water, electrolytes, bile acids, cholesterol, phospholipids and conjugated bilirubin.
Bowel obstruction         
  •  doi = 10.3791/1931 }}</ref>
  • Upright abdominal X-ray of a person with a large bowel obstruction showing multiple air fluid levels and dilated loops of bowel
  • A small bowel obstruction as seen on CT
  • Upright abdominal X-ray demonstrating a small bowel obstruction. Note multiple air fluid levels.
HUMAN DISEASE
Intestinal obstruction; Obstructed bowel; Intestinal Obstruction; Bowel blockage; Small bowel obstruction; Intestinal blockage; Large bowel obstruction; Causes of bowel obstruction
Bowel obstruction, also known as intestinal obstruction, is a mechanical or functional obstruction of the intestines which prevents the normal movement of the products of digestion. Either the small bowel or large bowel may be affected.
Primary biliary cholangitis         
LIVER CIRRHOSIS CHARACTERIZED BY CHRONIC AND SLOW PROGRESSIVE DESTRUCTION OF INTRAHEPATIC BILE DUCTS
Primary Biliary Cirrhosis; Biliary cirrhosis; Cholestatic liver disease; Hanot's disease; PBC Foundation; Primary biliary cirrhosis
Primary biliary cholangitis (PBC), previously known as primary biliary cirrhosis, is an autoimmune disease of the liver. It results from a slow, progressive destruction of the small bile ducts of the liver, causing bile and other toxins to build up in the liver, a condition called cholestasis.

Βικιπαίδεια

Biliary atresia

Biliary atresia, also known as extrahepatic ductopenia and progressive obliterative cholangiopathy, is a childhood disease of the liver in which one or more bile ducts are abnormally narrow, blocked, or absent. It can be congenital or acquired. It has an incidence of one in 10,000–15,000 live births in the United States, and a prevalence of one in 16,700 in the British Isles. Biliary atresia is most common in East Asia, with a frequency of one in 5,000.

The cause of biliary atresia in Egyptian infants has been proven to be as a result of aflatoxin induced cholangiopathy acquired prenatally in infants who have glutathione S transferase M1 deficiency. The biliary atresia phenotype caused by congenital aflatoxicosis in GST M1 deficient neonates is named Kotb disease. Syndromic biliary atresia (e.g. Biliary Atresia Splenic Malformation (BASM)) has been associated with certain genes (e.g. Polycystic Kidney Disease 1 Like 1 - PKD1L1), and some infants with isolated biliary atresia may arise as a result of an autoimmune inflammatory response, possibly due to a viral infection of the liver soon after birth. In animals plant toxins have been shown to cause biliary atresia. The only effective treatments are operations such as the Kasai procedure and liver transplantation.