Pancreas Flashcards
What is the most effective dose of pancreatic enzyme replacement for pancreatic insufficiency?
A starting dose of 40,000 to 50,000 USP units of lipase is recommended with dose increase up to 90,000 USP units of lipase based on response to treatment.
What is the differential for obstructive jaundice?
pancreatic cancer
-elevated IgG4
-atrophic pancreas
-dilated ducts
autoimmune pancreatitis
-elevated IgG4
-sausage-like pancreatic tissue with rim like hypoenhanement
-narrow bile ducts without marked upstream dilation
What are the features of autoimmune pancreatitis?
histology
imaging
serology
histology- lymphoproliferative infiltrate
imaging- pancreatic lesion with rim hypoenhancement, diffusely enlarged pancreas, can have biliary stricture
serology- elevated IgG4 >2x ULN, can also have elevated CA 19-9
What are the differences between AIP type 1 and type 2. Which is more likely to relapse?
Type 1- typically presents with painless jaundics, IgG4 related, associated with systemic disease (salivary gland, secondary sclerosing cholangitis, RP, lungs), high risk of relapse so may need maintenance, can use 1. pred or 2. rituximab
Tyle 2- typically presents with pancreatitis, low IgG4 levels, no systemic involvement, associated with iBD, low risk of relapse once treated
Autoimmune pancreatitis
diffusely enlarged pancreas, can also have areas of rim enhancement
can’t distinguish between type 1 or type 2 based on radiologic imaging alone
What are the features of chronic pancreatitis on EUS?
(Minimal standard terminology- MST)
lobularity
cysts
hyperechoic foci and strands
calcification of the duct
main PD dilation or irregularity
visible side-branches
What are the most common meds associated with acute pancreatitis?
AZA, 6-MP, ACE-I, valproate, lasix, cimetidine, estrogens, tetracycline, HCTZ, salicylates, metronidazole
Atlanta criteria
<4 weeks
acute peri-pancreatic fluid collection
acute necrotic collection
> 4 weeks
pseudocyst
WON
What are the genetic causes of pancreatitis?
PRSS1- AD inheritance
The following mutations predispose to pancreatitis
CFTR mutation > SPINK-1 (AR inheritance)
What are the diagnostic tests for pancreatic insufficiency?
fecal elastase <100, 72hr fecal fat >7g (while eating fat diet) - start with 40 to 50,000 U lipse/meal
fat soluble vitamin deficiencies
What are the complications of CPI?
osteoporosis
pancreatic ascites (amylase >1000) Rx with TPN and octreotide
splenic thrombosis and IGV - if h/o bleeding then get splenectomy
What is this and how is it managed?
Mucionus cystic neoplasm
CEA >200
low amylase
glucose <50
found in body and tail of pancreas
+malignant potential, surgical resection needed
IPMN
CEA >200
high amylase because connected to ducts
What are the worrisome features of an IPMN
-Main duct IPMN
-size >3cm
-enhancing mural nodule <5 = EUS, >5= surgery
-PD dilation >5 = EUS, >10 = -surgery
-growth >5mm/ 2 years
Serous cyst adenoma
multiple microcysts with a central scar (honeycomb appearance)
low CEA, low amylase
low malignant potential, only remove if symptomatic