Pancreas Flashcards
(35 cards)
work up and management for acute pancreatitis?
etiologies?
- 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
presents as MSOF, ARDS, hemodynamic instability, signs of
ecchymoses (Grey-Turner, Fox, Cullen signs)
dx? tx?
hemorrhagic pancreatitis
CT
admit to ICU for close monitoring
What are the
Grey-Turner sign
Cullen sign:
Fox sign:
Grey-Turner sign: flank ecchymoses
Cullen sign: periumbilical ecchymoses
Fox sign: ecchymoses of inguinal ligament
presents as abd pain and early satiety 2 wks s/p acute pancreatitis
dx and tx
pancreatic abcess
dx with CT scan
tx perc drain + IV abx
presents as abd pain and early satiety 5 wks s/p acute pancreatitis
dx and tx
pseudocyst
dx with CT
tx observation (5 cm)
chronic epigastric pain,
steatorrhea, diabetes mellitus
how to make dx? tx?
MC etiologies?
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)
dull abd pain + s/sx of obstructive jaundice (dark urine, clay stools, pruritus)
dx? tx? tumor marker?
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
what is the trousseau phenomenon?
migratory SVT in 10% of pancreatic cancer pts
what is the courvoisier sign?
palpable GB w/o pain in 30% of cancer pts
mass in pancreas + ↑insulin → Whipple’s triad (hypoglycemia, worse w/ fasting, better w/ glucose)
how to make dx? tx?
Insulinoma
Dx ↑C-peptide levels or monitored fasting (to see if they’re “faking it”)
Tx resection
how to work up suspected gastrinoma?
- get gastrin levels (500 tumor present)
- if btwn 200-500 get ecretin stimulation test (secretin releases gastrin from gastrinomas, it inhibits gastrin release from the normal stomach)
what is the gastrinoma triangle
neck of pancreas
cystic duct
junction b/t 2nd and 3rd part of duodenum
new-onset diabetes + necrolytic migratory erythema
how to work up?
glucagonoma
Dx with glucose challenge test
triad of gallstones, diabetes, steatorrhea
somatostatinoma
“rice water” diarrhea
VIPoma
presentation of MEN1 vs MEN2A and 2B
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
etiology of MEN2A and 2B
AD ret protooncogene
treatment for MEN1, 2A, 2B
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)
what is impaired glucose tolerace?
asx w/ fasting glc 110-126
how do T1DM typically present?
treatment for T1DM
in DKA
Tx
insulin, 0.5-1 u/kg (2/3 morning, 1/3 evening)
inpatient → Tx SSI
pathophys of T2DM
obesity → ↑FFA release → ↑insulin resistance → ↑glucose → classic sx (polyuria, polydipsia,
polyphagia) + blurry vision, weight loss, recurrent vaginal yeast infx
how to dx T2DM
Dx fasting glc >126
random glc >200 w/ sx
HbA1C >6.5%
how to manage T2DM
T2DM fasting glc 240 1st treat with insuin (still high) add another PO drug
what is monitoring schedule of T2DM as an outpatinet
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