Pancreas Flashcards

1
Q

work up and management for acute pancreatitis?

etiologies?

A
  • Dx screen w/ ↑lipase, confirm w/ CT scan
  • Tx NPO/IVF/pain meds

Etiology:
I GET SMASHED
Idiopathic

gallstones (#1),
EtOH (#2)
trauma

steroids
mumps,
autoimmune
scorpion sting,
hypertriglyceridemia (#3),
hypercalcemia
ERCP
drugs
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2
Q

presents as MSOF, ARDS, hemodynamic instability, signs of
ecchymoses (Grey-Turner, Fox, Cullen signs)

dx? tx?

A

hemorrhagic pancreatitis

CT

admit to ICU for close monitoring

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3
Q

What are the
Grey-Turner sign
Cullen sign:
Fox sign:

A

Grey-Turner sign: flank ecchymoses
Cullen sign: periumbilical ecchymoses
Fox sign: ecchymoses of inguinal ligament

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4
Q

presents as abd pain and early satiety 2 wks s/p acute pancreatitis

dx and tx

A

pancreatic abcess

dx with CT scan

tx perc drain + IV abx

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5
Q

presents as abd pain and early satiety 5 wks s/p acute pancreatitis

dx and tx

A

pseudocyst

dx with CT

tx observation (5 cm)

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6
Q

chronic epigastric pain,
steatorrhea, diabetes mellitus

how to make dx? tx?
MC etiologies?

A

chronic pancreatitis

Dx stool elastase test

Tx insulin + pancreatic enzyme replacement, IVF/NPO/pain meds for acute attacks

alcoholism (MCC adults), cystic fibrosis (MCC kids)

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7
Q

dull abd pain + s/sx of obstructive jaundice (dark urine, clay stools, pruritus)

dx? tx? tumor marker?

A

pancreatic cancer

Dx CT scan
Tx:
> cancer in head → Tx Whipple
> cancer in body or tail → Tx distal pancreatectomy
> mets or local invasion→ palliative care

    • f/u tumor markers CA 19
  • 9, CEA
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8
Q

what is the trousseau phenomenon?

A

migratory SVT in 10% of pancreatic cancer pts

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9
Q

what is the courvoisier sign?

A

palpable GB w/o pain in 30% of cancer pts

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10
Q

mass in pancreas + ↑insulin → Whipple’s triad (hypoglycemia, worse w/ fasting, better w/ glucose)

how to make dx? tx?

A

Insulinoma

Dx ↑C-peptide levels or monitored fasting (to see if they’re “faking it”)

Tx resection

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11
Q

how to work up suspected gastrinoma?

A
  1. get gastrin levels (500 tumor present)
  2. if btwn 200-500 get ecretin stimulation test (secretin releases gastrin from gastrinomas, it inhibits gastrin release from the normal stomach)
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12
Q

what is the gastrinoma triangle

A

neck of pancreas
cystic duct
junction b/t 2nd and 3rd part of duodenum

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13
Q

new-onset diabetes + necrolytic migratory erythema

how to work up?

A

glucagonoma

Dx with glucose challenge test

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14
Q

triad of gallstones, diabetes, steatorrhea

A

somatostatinoma

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15
Q

“rice water” diarrhea

A

VIPoma

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16
Q

presentation of MEN1 vs MEN2A and 2B

A

MEN1: pituitary adenoma, pancreatic endocrinoma (MC gastrinoma), parathyroid hyperplasia

MEN2A: parathyroid hyperplasia,
pheochromocytoma, thyroid
medullary cancer

MEN2B: pheochromocytoma, thyroid medullary cancer, mucosal
neuromas, Marfanoid habitus

17
Q

etiology of MEN2A and 2B

A

AD ret protooncogene

18
Q

treatment for MEN1, 2A, 2B

A

MEN1: Tx excise parathyroid first (since hyper calcemia can cause ↑gastrin), then gastrinoma, then pituitary adenoma (w/ cabergoline)

MEN2A and B: excise pheo first (life threatening)

19
Q

what is impaired glucose tolerace?

A

asx w/ fasting glc 110-126

20
Q

how do T1DM typically present?

treatment for T1DM

A

in DKA

Tx
insulin, 0.5-1 u/kg (2/3 morning, 1/3 evening)

inpatient → Tx SSI

21
Q

pathophys of T2DM

A

obesity → ↑FFA release → ↑insulin resistance → ↑glucose → classic sx (polyuria, polydipsia,
polyphagia) + blurry vision, weight loss, recurrent vaginal yeast infx

22
Q

how to dx T2DM

A

Dx fasting glc >126
random glc >200 w/ sx
HbA1C >6.5%

23
Q

how to manage T2DM

A
T2DM
fasting glc  240 
  1st treat with insuin 
      (still high) 
  add another PO drug
24
Q

what is monitoring schedule of T2DM as an outpatinet

A
q day – glucose
q visit – BP, foot chk
q 3 mo – HbA1c
q 6 mo – neuropathy chk
q yr – microalbuminuria, BUN/Cr, lipids, eye chk
25
Q
ideal levels of ...  for T2DM
HbA1c
fasting glc
post-prandial glc 
BP 
LDL
A

HbA1c <100

26
Q

pathophys of macrovascular disease in DM

Ppx?

A

nonenzymatic glycosylation → atherosclerosis

PPx reduction of risk factors (BP, lipids, smoking, diet, exercise)

27
Q

Pathophys of diabetic nephropathy?

Ppx? Tx?

A

non-enzymatic glycosylation of BM → loss of negative charge → microalbuminuria → proteinuria → CKD → ESRD

PPx annual microalbuminuria screening

Tx ACE inhibitors

28
Q

Pathophys of diabetic retinopathy?

ppx? tx?

A

NEG of retinal vx → either background or proliferative retinopathy

PPx annual ophtho referral

Tx photocoagulation

29
Q

Pathophys of diabetic neuropathy?

tx?

A

NEG of peripheral nerves → damage → “stocking/glove” burning pain, numbness, tingling

  • neuropathy → Tx amitriptyline (1st line), gabapentin or duloxetine (2nd line)
  • gastroparesis → Tx metoclopramide
30
Q

pathophys of diabetic foot?

Ppx? Tx?

A

peripheral neuropathy + PVD (ischemia) → repetitive injuries → ulcers and nonhealing

PPx regular foot check

Tx wound care, amputation (last resort)

31
Q

“T1DM exacerbation” = ?
pathophys + s/s?
how to dx?
tx?

A

DKA

↓insulin → hyperglycemia + ketosis → osmotic diuresis, dehydration, fruity breath, Kussmaul respiration, etc.

Dx ↑glc, ↑ketones, metabolic acidosis

Tx insulin + IVF (NS) + potassium (paradoxical)

32
Q

“T2DM exacerbation” =

pathophys + s/s?
how to dx?
tx?

A

T2DM exacerbation

↓insulin → hyperglycemia → hyperosmolarity, osmotic diuresis,
severe dehydration

Dx ↑glc, ↑osmolarity, no acidosis or ketosis

Tx insulin + IVF (NS)

33
Q

get SNS dysfunction w/ blood glc of ___

A

40-50 (HA, weakness, drowsiness, coma)

34
Q

MCC etiology hypoglycemia

A
insulin overdose (MCC),
factitious hypoglycemia (low Cpeptide levels), insulinoma, etc
35
Q

how to work up hypoglycemia? Tx?

A

Dx C-peptide, insulin levels, anti-insulin ab, and sulfonylurea levels (look for underlying cause)

Tx underlying cause + sugary foods or IV D50W