CH 8 Pediatric Pancreas Flashcards
Pancreas
retroperitoneal structure. functions as an endocrine and exocrine gland.
Endocrine function: secrete insulin via the islets of langerhans.
Exocrine function: secrete trypsin, lipase and amylase.
Pancreas location
Pancreas lies between the splenic hilum and the duodenal loop. the GDA is anterolateral to the pancreatic head and the CBD is posterolateral to the pancreatic head. The SMA/SMV are posterior to the neck of the pancreas and anterior to the uncinate process. the splenic artery courses along the superior border of the pancreas and the splenic vein is posterior.
Duct of Wirsung
main pancreatic duct.
courses through the pancreas and joins the CBD to form the ampulla of Vater which empties into the 2nd portion of the duodenum.
Duct of santorini
accessory pancreatic duct, empties into the duodenum, proximal to the ampulla of Vater.
*Pancreas divisum
occurs when the ventral and dorsal pancreatic buds do not fuse and each maintains a separate duct. This results in a smaller duct of santorini which may cause pancreatitis due to inadequate pancreatic enzyme drainage.
Pancreatic cysts
true pancreatic cysts are rare. They are associated with ADPKD, von hippel - lindau and cystic fibrosis.
congenital cysts of the pancreas are caused by anomalous development of the pancreatic ducts.
Annular pancreas
ventral segment of the developing pancrease encircles the duodenum and forms a ring of pancreatic tissue causing and obstruction of the gastric outlet. (2nd most common panc anomaly)
more common in males
Annular pancreas associated with congenital disorders:
Down’s syndrome, TEF (tracheoesophageal fistula), intestinal atresia and pancreas divisum.
Ectopic pancreas
lies in the submucosal position and occurs around the antrum of the stomach.
associated with: VATER syndrome, gut malrotation, and duodenal atresia.
Nesidioblastosis
persistence of the fetal state of the pancreas.
Nesidioblast secrete insulin.
babies present with HYPOglycemia
Effect of cystic fibrosis on pancreas
85% of children with cystic fibrosis have pancreatic insufficiency, which leads to steatorrhea (fat in feces) and malabsorption. Ducts become dilated and cause small cysts and fibrosis of pancreas.
*thickened mucus lines pancratic, bronchial, and biliary ducts.
obstruction and distention lead to: degeneration, atrophy, insufficiency, fibrosis, and fatty replacement.
Sono: increase in echogenicity and decrease in size
Schwachman syndrome:
causes: pancreatic insufficiency (2nd most common), and fatty infiltrate of pancreas.
sono: normal hyperechoic pancreas
Syndrome includes: metaphyseal chondroplasia (shortening of extremities), metaphyseal widening “cupping” of the ribs and bone marrow hypoplasia, enlarged spleen.
Acute pancreatitis
usually due to blunt abdominal trauma or non-accidental injury (child abuse)
can be caused by: mumps, drug toxicity and biliary and pancreatic anomalies.
sono: pancreas appears hypoechoic and edematous
* trauma due to child abuse is the most common cause in children.
Pancreatitis symptoms:
constant, severe epigastric or periumbilical pain which radiates to the back and shoulders nd the patient has raised amylase levels.
rest, and oral feedings must be stopped.
Chronic pancreatitis
repeated attacks of pancreatitis and is NOT reversible.
sono: pancreas usually small due to fibrosis and appears heterogeneous. calcifications may be present and dilatation of the pancreatic duct and CBD is common.