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97 Cards in this Set

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think liver biopsy for diagnosis of (at least) the following:
cirrhosis

hc

[wilson's dz -- can be helpful, I'm not sure if it's necessary]

hemochromatosis
don't biopsy this liver prob...

why?
cavernous hemangiomas

rupture / hemorrhage
liver transplant is helpful for (at least) the following
hepatorenal syndrome

if med rx isn't enough:
-- wilson's
-- hemochromatosis

HCC unless you're one of the 10% of resectable pts
the gold standard for diagnosis of cirrhosis
liver biopsy
_ estimates severity of liver dz
child's classification
child's classification: class A (the best) features
no ascites
bili < 2.0
no encephalopathy
excellent nutritional status
albumin > 3.5
bilirubin in mild vs. severe liver dz
< 2.0

> 3.0
albumin in mild vs. severe liver dz
> 3.5

< 3.0
bilirubin in severe liver dz
> 3.0
albumin in severe liver dz
< 3.0
11 causes of cirrhosis

grouped to help me remember them
nonalcoholic steatohepatitis
------
alcohol
acetaminophen, methotrexate

hepatitis b & c
------
autoimmune hepatitis
primary biliary cirrhosis, secondary biliary cirrhosis

hemochromatosis
Wilson's
AAT deficiency

hepatic congestion 2^
-- right-sided heart failure
-- constrictive pericarditis

hepatic veno-occlusive dz
-- e.g. after marrow transplant
what % of heavy drinkers develop cirrhosis
15-20%
drugs that cause cirrhosis
acetaminophen
methotrexate
treatment for bleeding varices includes
IV octreotide

variceal ligation

[endoscopic sclerotherapy]
two meds for acutely bleeding esophageal varices, and which one is better and has replaced the other one
octreotide -- less s/e
vasopressin
ascites can be managed by _____ in most cases
salt restriction and diuretics
prophylactic medication for esophageal varices
nonselective beta blocker
______ (a complication of cirrhosis) can exacerbate hepatic encephalopathy
varices -- ? bleeding or not ?
initial treatment for bleeding varices
fluids
treatment for varices acutely
IV fluids
IV antibiotics prophylactically
IV octreotide
emergent upper GI endoscopy for either
-- *ligation*
-- [sclerotherapy]
the most common complication of cirrhosis
ascites
ascites in cirrhosis is due to
portal HTN
hypoalbuminemia
ascites sxs
abdominal distention
shifting dullness
fluid wave
if you suspect pt. has ascites, what do you do diagnostically?
paracentesis to determine if it's due to portal htn vs. something else
indications for diagnostic paracentesis
new-onset ascites
worsening ascites
spontaneous bacterial peritonitis
differential diagnosis of causes of ascites

(10)
cirrhosis
portal htn
chf
massive fluid overload

chronic renal dz
hypoalbuminemia

tuberculous peritonitis
malignancy


endotoxin -->
NO release -->
peripheral vasodilation -->
^ renin -->
^ aldosterone

impaired liver inactivation of aldosterone
a key lab value in discerning the cause of ascites
serum ascites albumin gradient

if > 1.1 g/dL, portal HTN is likely the cause
when doing diagnostic paracentesis, you want to rule out ______ by
spontaneous bacterial peritonitis

Gram stain and culture
treatment for ascites
bed rest
low-sodium diet
furosemide
spironolactone

paracentesis if
-- tense
-- shortness of breath
-- early satiety

TIPS/peritoneovenous shunt
precipitants of hepatic encephalopathy (7)
alkalosis
hypokalemia
-- e.g. 2^ diuretics

GI bleeding
hypovolemia

narcotics
sleeping pills

systemic infection
monitor cirrhosis pts by.,..
labs every 3-4 months:

CBC

renal function tests / electrolytes

LFTs, coags

- - - - - - - - - - - - - - - - -

endoscopy to determine presence of varices
cirrhosis pts:

if carcinoma is suspected, perform a....
CT-guided biopsy
treatment for hepatic encephalopathy and why
lactulose
-- its metabolism by bacteria favors NH4+ formation, which is poorly absorbed vs. NH3

neomycin
-- kills bowel flora --> v ammonia production

limit protein to 30 to 40 g/day
-- reduces production of NH3 in the first place
mechanism of hepatorenal syndrome
splanchnic vasodilation -->
kidney hypoperfusion -->
RAAS -->
vasoconstriction of renal vessels -->
renal hypoperfusion
this gi problem does not respond to volume expansion
hepatorenal syndrome
hepatorenal syndrome rx
liver transplantation is the only cure
hepatorenal syndrome 5 lab findings
azotemia
oliguria

hyponatremia
hypotension
U Na+ < 10 (low)
if you see

fever
change in mental status

in an ascites pt

think
spontaneous bacterial peritonitis
most common causes of spontaneous bacterial peritonitis
E coli
Klebsiella
Streptococcus pneumoniae
diagnosis of spontaneous bacterial peritonitis
paracentesis

-- WBC > 500
-- PMN > 250
+ culture, or culture-negative
spontaneous bacterial peritonitis initial rx
broad spectrum abx
-- give specific antibiotic once organism is identified
cirrhosis hyperestrinism signs
spider angiomas
palmar erythema
gynecomastia
testicular atrophy
cirrhosis

coagulopathy lab values
^ PT
treat coagulopathy in cirrhosis with
fresh flozen plasma
genetics of wilson's dz
recessive
genetics of hemochromatosis
recessive
wilson's disease molecularly:
deficiency of ceruloplasmin
wilson's dz most common initial manifestation
liver dz
how does wilson's dz affect the eye
kayser-fleischer rings
-- yellowish rings in cornea

they do not interfere with vision
organ systems affected by wilson's dz
liver
eye
brain
renal
how does wilson's dz affect kidneys
aminoaciduria
nephrocalcinosis
how does wilson's dz affect the brain
parkinsonian sxs
-- resting tremor
-- rigidity
-- bradykinesia

chorea
drooling
incoordination

depression
personality changes
psychosis
where does copper deposit in the brain in wilson's dz
basal ganglia
wilson's dz diagnosis -- (a few to many of the following may be present)
^ aminotransferases

v coags
v albumin

v serum ceruloplasmin
^ copper on liver biopsy
treatment for wilson's dz
D-penicillamine
zinc

liver transplantation if unresponsive to the above
hemochromatosis pathophys
excessive iron absorption in the intestine -->

accumulation of iron (as ferritin and hemosiderin) in various organs -->

hydroxyl free radicals -->

fibrosis
secondary hemochromatosis can occur with
multiple transfusions
chronic hemolytic anemias
early in dz course of hemochromatosis

you may find _____

next diagnostic steps?
elevated ALT, AST


iron studies. if elevated -->

liver biopsy
complications of hemochromatosis
cirrhosis
-- carcinoma risk x 200

CHF
arrhythmias


2nd and 3rd metacarpophalangeal joints
hips
knees

hyperpigmentation of skin
-- like sun tan, "bronzelike"


diabetes
hypogonadism
hypothyroidism
diagnosis of hemochromatosis
^ ALT, AST

^ serum iron
^ serum ferritin
^ transferrin saturation
v TIBC

liver biopsy
_____ is required for the diagnosis of hemochromatosis
liver biopsy
treatment for hemochromatosis
repeated phlebotomies

treat complications

liver transplantation in advanced cases
hepatocellular adenoma

seen in which pts / why
women
15-40 yrs

oral contraceptives
anabolic steroids
a couple complications / sequelae of hepatocellular adenoma
malignancy (<1%)

rupture --> hemoperitoneum, hemorrhage
diagnosis of hepatocellular adenoma
CT scan
ultrasound
hepatic arteriography
hepatocellular adenoma rx
discontinue oral contraceptives
surgically resect tumors > 5cm
the most common type of benign liver tumor
cavernous hemangiomas
cavernous hemangiomas size may increase due to
pregnancy
oral contraceptives
cavernous hemangiomas diagnosis
ultrasound
CT scan with IV contrast
cavernous hemangiomas: do not do ____ for diagnosis
biopsy
biopsy is contraindicated in this benign tumor
liver cavernous hemangiomas
there is no association of ______ with oral contraceptives
focal nodular hyperplasia
risk factors for hepatocellular carcinoma
cirrhosis
-- alcohol
-- hepatitis B & C

aflatoxin, vinyl chloride, Thorotrast

AAT deficiency
Hemochromatosis
Wilson's dz

schistosomiasis
hepatic adenoma
smoking
glycogen storage dz type 1
distinctive clinical features of HCC
painful hepatomegaly

erythrocytosis
thrombocytosis

hypercalcemia
hypoglycemia
high cholesterol

carcinoid syndrome
hypertrophic pulmonary osteodystrophy
HCC can --> ^ / v this electrolyte
hypercalcemia
how does HCC affect cholesterol?
high cholesterol
how does HCC affect glucose?
hypoglycemia
think HCC if you see (3)
cirrhosis
palpable liver mass
^ AFP
_____ is required for definitive diagnosis of HCC
liver biopsy
HCC:

if surgery is an option, do this as part of the diagnostic regimen b/c
MRI
MRA

they provide more detail about the tumor's anatomy
gilbert's syndrome genetics
autosomal dominant
gilbert's syndrome is due to
v activity of uridine diphosphate glucuronyl transferase
a couple common causes of unconjugated bilirubin
hemolysis
Gilbert's syndrome
causes of hemobilia
trauma (most common)
papillary thyroid carcinoma
surgery
tumors
infection
diagnosis of hemobilia
arteriogram

upper GI endoscopy shows blood coming out of ampulla of Vater
hydatid liver cysts are caused by
Echinococcus granulosus
Echinococcus multilocularis
hydatid liver cysts rx
surgery

(avoid spilling contents of the cyst into the peritoneal cavity)

mebendazole
what's dangerous about hydatid liver cysts?
larger cysts may cause

rupture --> fatal anaphylactic shock
treatment for hydatid liver cysts is ____

treatment for amebid liver abscess is ____
mebendazole

IV metronidazole
most common causes of pyogenic liver abscess
biliary tract obstruction (most common cause)

GI infection
-- diverticulitis
-- appendicitis

penetrating liver trauma
diagnosis of pyogenic liver abscess
US
CT scan

^ LFTs
prognosis of liver abscess
fatal if untreated
liver abscess rx
IV antibiotics
percutaneous drainage
amebic liver abscess

which pts?

why?
homosexual men

fecal-oral contact
amebic liver abscess is caused by
Entamoeba histolytica
amebic liver abscess dx
immunoglobulin G enzyme immunoassay
amebic liver abscess rx
IV metronidazole