evaluating abnormal liver enzymes - rutland

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Last updated 6:39 PM on 4/15/26
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61 Terms

1
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what is not one of the functions of the liver?

production of liver enzymes

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T/F: liver enzyme measurements are liver function tests

F

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liver function tests

albumin

bilirubin

INR

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two patterns of liver enzyme elevation

hepatocellular AST/ALT

cholestatic ALP

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meds, alcohol

viral hepatitis

hemochromatosis

autoimmune hep

wilsons

alpha 1 antitrypsin def

steatosis

hepatocellular

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meds alcohol

obstruction

tumors

primary biliary cholangitis

primary sclerosing cholangitis

granulomatous liver disease

cholestatic

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strategy for hepatocellular

serolgoic evaluation

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strat for cholestatic

imaging studies

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common culprits of med induced liver disease

OTC and supplements

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drug induced liver injury diagnosis

exclusion

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AST:ALT ratio of 2:1 or 3:1

AST and ALT NEVER >500 IU, rarely over 200 IU

alcoholic liver disease

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liver assoc enzymes (LAE) >500 and <1500

viral hepatitis

med toxicity

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LAE >2000

acetaminophen toxicity

ischemic injury

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AST:ALT ratio in hepatocellular disease: chronic viral hep

variable, ~1

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excess iron accumulation in organs

hemochromatosis

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hemochromatosis diagnosis

elevated transferrin sat

C282Y homozygous (genetic testing)

<p>elevated transferrin sat</p><p><strong>C282Y homozygous </strong>(genetic testing) </p>
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elevated ALT, AST (>10X ULN)

increased gamma globulin

increased IgG

low albumin, prolonged prothrombin time

autoimmune hepatitis

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autoimmune hepatitis diagnosis

ANA

SMA

liver biopsy

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ANA, SMA

pANCA, SLA/LP

all ages

thyroiditis, UC, snyovitis

tx failure uncommon

type 1 AI hepatitis

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antiLKM1

anti LC1

2-14 yrs

vitiligo, T1DM, thyroiditis

tx failure common

type 2 autoimmune hepatitis

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<p>low ALP + AST:ALT high (up to 4:1) in a young patient</p>

low ALP + AST:ALT high (up to 4:1) in a young patient

wilsons disease

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decreased ceruloplasmin, increased 24h urine copper

wilsons disease

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liver + pulmonary disease (early lower lobe emphysema)

a1 antitrypsin deficiency

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diagnosis for a1 antitrypsin def

dec antitrypsin level

PiZZ phenotype

PAS-D positive globules

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<p>PAS stain after diastase digestion</p>

PAS stain after diastase digestion

alpha 1 antitrypsin globules

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small bowel disease, sensitive to gliadin

inflammation, epithelial damage, malabsorption

liver → innocent bystander

celiac sprue

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isolated increased liver enzymes

unexplained transaminitis

celiac

28
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elevated liver enzymes, negative diagnositc evaluation

female, obese, diabetic

hepatic steatosis

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hepatic manifestation of metabolic syndrome

fatty liver:

  1. increased abdominal girth (m >40, f >35)

  2. elevated triglycerides (>150

  3. low hdl (m <40, women <50)

  4. hyperglycemia (FBS >= 100)

    1. HTN (>130/85)

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fat without inflammation, good prog rare progress

steatosis fatty liver

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fat WITH inflammation, may progress to cirrhosis

steathepatitis

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hepatic steatosis

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steatohepatitis

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steatohepatitis, pericellular fibrosis

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steatohepatitis cirrhosis

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may become most common cause of cirrhosis, sig cardiac morbidity and mortality

FAtty liver disease/MAFLD

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approach to elevated LFTs

history (med and alcohol)

hep b and c serologies

iron studies

ceruloplasmin, urine coppers

a1antittrypsin phenotype

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cholestatic injury initial eval

exclude biliary obstruction and liver mass lesions

RUQ US

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common cause cholestatic injury

drug induced liver injury

stop sus meds

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first step in cholestatic patterns

RUQ US

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AI disorder of biliary epithelium

pruritus and hepatomegaly

asymptomatic AP elevation

primary biliary cholangitis

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diagnosis for primary biliary cholangitis

antimitochondrial antibody (AMA)

Lab: marked AP elevation

biopsy: unusual

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tx for PBC

ursodeoxycholic acid

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immune mediated destruction of small intrahepatic bile ducts

PBC

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PBC florid duct lesion

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first line therapy for PBC

UDCA, improves cholestasis and lipid profile

safe and well tolerated

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autoimmune disorder men and women

assoc with IBD

ASx AP elevation

RUQ pain, fever, jaundice

PSC [rimary sclerosing cholangitis

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PSC diagnosis

endoscopic retrograde cholangiopancreatiography or MRCP

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progressive inflammatory fibrosis and destruction of intra and extra hepatic bile ducts

80% have IBD

PSC

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increased malignancy risk

  • cholangiocarcinoma

  • colon cancer

  • HCC

  • pancreatic cancer

PSC, colonscopy every year

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PSC diagnosis

cholestatic liver profile

cholangiography

pANCA 65-80%

liver biopsy rarely diagnostic - 10% onion skin

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PSC

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PSC

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alright

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PBC and PSC AI disorders

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clinical features compare

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lab findings

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most common causes of granulomatous liver disease

meds and sarcoidosis

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granulomatous liver disease

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approach to cholestatic liver enzyme elevation

history

abdominal US

AMA test

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elevation of Alk Phos