22 - Chronic Liver Disease Flashcards

1
Q

time minimum for chronic liver disease

A

6 mo

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2
Q

vertical transmission of hep B

A

leads to chronic dz in 90% of cases (as opposed to 5% in adults)

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3
Q

antibody assoc w/ immunity to Hep B (either cleared past infxn or got vaccine)

A

Anti-HB surface

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4
Q

antibody assoc w/ current or past infxn w/ Hep B

A

Anti-HB core

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5
Q

how many chronic Hep C pts get cirrhosis? hepatocellular CA?

A

cirrhosis - 20-30%

CA - 1-5% of those w/ cirrhosis

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6
Q

anti HCV ab significance

A

present during active infection, does not confer immunity, will go away in pts that get over acute infection and dont become chronic carriers

basically if they have it, they probably have (or just recently had) hep C

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7
Q

path processes occurring in acute hepatitis

A
necrosis of hepatocytes
ballooning degen, lobular disarray
kupffer cell hyperplasia/hypertrophy
portal inflammation (lymphs)
regeneration in recovery phase
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8
Q

differences in chronic hepatitis path compared to acute

A

mostly the same, but in chronic more inflammation (lymphs) including interface hepatitis
also develop fibrosis which can progress to cirrhosis

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9
Q

ground glass cytoplasmic change in liver

A

HbSurface Antigen or any prolif of smooth ER (due to drugs, w/e)

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10
Q

autoimmune hepatitis

A

T cell attack on hepatocytes
looks like chronic viral hepatitis
mostly affects young females
often presents as aggressive disease

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11
Q

lab findings in autoimmune hepatitis

A

elevated IgG and transaminases

elevated autoantibodies - ex ANA

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12
Q

primary biliary cirrhosis

A

destruction of intrahepatic interlobular bile ducts > eventual cirrhosis and liver failure
unk etiology but may be autoimmune

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13
Q

clues to dx primary biliary cirrhosis

A

elevated alk phos
pruritis often early symptom
mostly affects middle age women
antimitochondrial antibodies in 95%

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14
Q

primary sclerosing cholangitis

A

mostly males
70% have ulcerative colitis
inc risk for cholangioCA
concentric peri-bile duct fibrosis > obstruction

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15
Q

alcoholic liver disease - more often macro or microvesicular steatosis?

A

macro

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16
Q

3 components of cirrhosis

A

fibrosis
loss of nl architecture
regenerative nodules

17
Q

associated etiologies of micronodular, finely nodular, and macronodular cirrhosis

A

micro - alcohol
finely - biliary
macro - viral hepatitis, hemochromatosis

18
Q

3 MCC cirrhosis in western world

A

alcoholism
viral hepatitis
nonalcoholic steatohepatitis

19
Q

prehepatic, hepatic, and post hepatic etiology of portal HTN

A

pre - thrombosis of portal/umbilical vein
hepatic - cirrhosis
post - right HF

20
Q

clinical consequences of portal HTN

A

ascites
varices (portosystemic venous shunts)
congestive splenomegaly
hepatic encephalopathy