Pancreas Flashcards

1
Q

What is the most effective dose of pancreatic enzyme replacement for pancreatic insufficiency?

A

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.

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2
Q

What is the differential for obstructive jaundice?

A

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

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3
Q

What are the features of autoimmune pancreatitis?
histology
imaging
serology

A

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

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4
Q

What are the differences between AIP type 1 and type 2. Which is more likely to relapse?

A

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

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5
Q
A

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

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6
Q

What are the features of chronic pancreatitis on EUS?

A

(Minimal standard terminology- MST)
lobularity
cysts
hyperechoic foci and strands
calcification of the duct
main PD dilation or irregularity
visible side-branches

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7
Q

What are the most common meds associated with acute pancreatitis?

A

AZA, 6-MP, ACE-I, valproate, lasix, cimetidine, estrogens, tetracycline, HCTZ, salicylates, metronidazole

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8
Q

Atlanta criteria

A

<4 weeks
acute peri-pancreatic fluid collection
acute necrotic collection

> 4 weeks
pseudocyst
WON

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9
Q

What are the genetic causes of pancreatitis?

A

PRSS1- AD inheritance

The following mutations predispose to pancreatitis
CFTR mutation > SPINK-1 (AR inheritance)

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10
Q

What are the diagnostic tests for pancreatic insufficiency?

A

fecal elastase <100, 72hr fecal fat >7g (while eating fat diet) - start with 40 to 50,000 U lipse/meal

fat soluble vitamin deficiencies

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11
Q

What are the complications of CPI?

A

osteoporosis

pancreatic ascites (amylase >1000) Rx with TPN and octreotide

splenic thrombosis and IGV - if h/o bleeding then get splenectomy

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12
Q

What is this and how is it managed?

A

Mucionus cystic neoplasm

CEA >200
low amylase
glucose <50
found in body and tail of pancreas

+malignant potential, surgical resection needed

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13
Q
A

IPMN

CEA >200
high amylase because connected to ducts

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14
Q

What are the worrisome features of an IPMN

A

-Main duct IPMN
-size >3cm
-enhancing mural nodule <5 = EUS, >5= surgery
-PD dilation >5 = EUS, >10 = -surgery
-growth >5mm/ 2 years

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15
Q
A

Serous cyst adenoma

multiple microcysts with a central scar (honeycomb appearance)
low CEA, low amylase
low malignant potential, only remove if symptomatic

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16
Q
A

Serous cyst adenoma
multiple microcysts with a central scar (honeycomb appearance)
low CEA, low amylase
low malignant potential, only remove if symptomatic

17
Q
A

Solid pseudopapillary neoplasm

young women
low cea and amylase
solid and cystic components
+malignancy, remove and annual surveillance

18
Q

How are cholesterol gallstones made?

A

supersaturation and nucleation grown
cholesterol crystal

19
Q

How are pigmented stones made?

A

precipitation
made from calcium bilirubinate
Black- unconjucated bili (i.e. hemolytic anemia, SC)
Brown= stasis or infection, often seen >2 years after cholecystectomy

20
Q

What are the indications for cholecystectomy?

A

-porcelain GB (GB wall calcifications)
-APBJ
-Polyp >8cm in PSC or >10cm in avg risk (follow with US q6-12 mo)
-use of somatostatin analog in pt with gallstones
-chronic salmonella

21
Q

What are the causes of bile leak after cholcystectomy?

A

cystic duct stump

ducts of luschka (from R IH ducts that connect directly with gb)

22
Q

What are the high risk and int risk criteria for choledocho?

A

HIGH RISK
-stone visualized
-cholangitis
-TB >4 and CBD >6 w/ GB or >8 w/o GB

INT RISK
-age >55
-abnormal LFTs
-CBD dilated

23
Q

how do you remove a CBD stone >1cm?

A

sphincterotomy and large balloon transpapillary dilation

24
Q

What is the rome criteria for sphincter of oddi dysfunction?

A

Need all 3
-biliary pain
-AST/ALT >3x ULN
-CBD>10
Perform sphincterotomy

suspected SOD
-biliary pain
-either increased LFTs or CBD dilation
controversial- ERCP +/- manometry

25
Q

What are the RF for shpincter of oddi dysfunction?

A
  1. after cholecystecomy with ongoing biliary colic
  2. recurrent idopathic pancreatitis
  3. biliary pain in pt with GB intact and no gallstone (controversial)
26
Q

What is the typical presentation for choledochal cysts and what are they associated with?

A

jaundice, fever, pancreatitis, pain

associated with APBJ, cholangio, GB cancer, pancreatic cancer

27
Q

Describe the 5 types of choledochal cysts and how they are treated.

A

Type 3 can be treated with sphincterotomy, the rest need surgery

28
Q

What are the common causes of bile duct leak and how are they managed?

A

Large biloma needs PTC

post CCY- cystic duct stpump >ducts of lushka; Rx with plastic stent x 4 weeks, CHD injury = surgery

post OLT- plastic stent

trauma/liver injury

29
Q

How to manage hilar strictures?

A

Get MRI then EUS/FNA

don’t routinely stent with ERCP, just sent to surgery

30
Q
A

Type 3 choledochal cyst

31
Q

What is the most common GI manifestation in cystic fibrosis?

A

exocrine insufficiency

32
Q

What is a functional test for chronic pancreatitis?

A

Pancreatic function testing with secretin can assess pancreatic ductal function by measuring duodenal concentrations of bicarbonate after intravenous administration of secretin.

33
Q

pancreatic lesions in Von Hippel-Lindau disease

A

pancreatic abnormalities, with pancreatic cysts being the most common. These are most commonly serous cystadenomas and thus not at risk of malignant transformation.