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acini cells
perform exocrine functions
small sac clusters connected by small ducts that connect to large excretory ducts
Up to 2L of juice made per day
Amylase
carb digesting enzyme
Duct of Santorini
drains upper anterior head
enters duodenum at minor papilla
secondary duct
duct of wirsung
extends entire length of gland
enters duodenum at ampulla
primary duct
duct of wirsung
measures 2mm or less
endocrine
hormonal function
exocrine
digestive function
glucagon
formed by alpha cells in islets
hormone that makes cells release glucose
stimulates liver to convert stored glycogen to released glucose to increase sugar levels
Hypercalcemia
elevated calcium levels
predisposed to chronic pancreatitis
Hyperlipidemia
elevated fat levels
predisposed to chronic pancreatitis
insulin
produced by beta cells
islets of langerhans
used in endocrine functions
hold specialized Alpha, Beta, and Delta cells
lipase
enzyme that digests fats
ascites
occurs when pseudocyst ruptures into the abdomen
pseudocyst
walled-off fluid collection caused from inflammation, necrosis, trauma, and hemorrhage
uncinate process
small curved tip at end of head
celiac axis
three branches: left gastric, common hepatic, and splenic arteries
originates from anterior abdominal aorta
superior mesenteric artery
from aorta, courses anterior
enters 3rd portion of duodenum to enter small bowel mesentery
pancreas divisum
rare congenital condition
caused by lack of fusion of dorsal and ventral pancreatic buds
ectopic pancreatic tissue
congenital anomaly showing intramural nodules
can be found throughout GI tract
feel like polyps with central dimple
0.5-2cm tumors and acute pancreatitis can occur in them
annular pancreas
rare anomaly where head surrounds second portion of duodenum
courvoisier sign
jaundice w/ gallbladder hydrops (gallbladder dilation)
acute pancreatitis
inflamed acini cells release enzymes into surrounding tissue
usually come w/ history of gallstones or alcoholism
hypoechoic texture
irregular borders
enlarged head and pancreatic duct
gallstones
fluid collection
leukocytosis
hemorrhagic pancreatitis
rapid progression of acute pancreatitis with rupture of pancreatic vessels
phlegmonous pancreatitis
hypoechoic texture
irregular borders
enlarged head and pancreatic duct
HYPOECHOIC ILL-DEFINED MASS
gallstones
fluid collection
leukocytosis
pancreatic absess
develops often post-op
related to necrosis and nearby infection
HYPOECHOIC MASS W/ SMOOTH BORDERS
THICK WALLS
increased leukocytosis
chronic pancreatitis
recurrent acute pancreatitis attacks causing permanent damage
limited endocrine and exocrine functioning
weight loss
fatty stool
diabetes signs
SMALL FIBROTIC GLAND
MIXED ECHOGENICITY
JAUNDICE
increased enzymes
autosomal polycystic disease
multiple cysts in kidney and liver extending to pancreas
von hippel-lindau syndrome
formation of tumors and cysts around the body
inherited disorder
insulinoma
islet cell tumor
B-cell tumor
gastrinoma
islet tumor than produces Zollinger-Ellison syndrome
caused by non-insulin tumors
G-cell tumor