Adult liver disease Flashcards

(49 cards)

1
Q

lymphocyte inflammation in hepatitis

A

can be present in many hepatitides; common in VIRAL

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2
Q

neutrophil inflammation in hepatitis

A

common in steatohepatitis

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3
Q

eosinophil inflammation in hepatitis

A

common in drug injury

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4
Q

plasma cell inflammation in hepatitis

A

autoimmune hepatitis

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5
Q

most common cause of chronic liver disease

A

hep C

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6
Q

Labs: evidence of hepatocyte injury

causes: acute viral infection and drug injury
histology: lobular disarray, marked inflammation throughout, widespread hepatocyte injury, NO FIBROSIS

A

acute hepatitis

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7
Q

Causes: chronic viral hepatitis, autoimmune hepatitis, drug injury

histology: less inflammation and injury, portal tract-based inflammation, FIBROSIS

long-standing ( > 6 mo)

A

chronic hepatitis

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8
Q

can accumulate in hepatocyte cytoplasm during liver injury

A

fat = steatosis
bile = cholestasis
iron = hemosiderosis/genetic hemochromatosis
copper = wilson disease/chronic cholestasis
viral particles = viral hepatitis

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9
Q

ground glass hepatocytes

A

viral infection

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10
Q

process of fibrotic change in hepatocytes

A

chronic cycles of injury/regeneration –> activated stellate cells deposit collagen –> architectural and vascular reorganization –> cirrhosis

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11
Q

On biopsy, “stage” refers to:

A

amount of fibrous tissue deposition

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12
Q

On biopsy, “grade” refers to:

A

amount of inflammation and injury

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13
Q

transmitted fecal-oral

A

hep A, hep E

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14
Q

transmitted through parenteral, sexual contact, perinatal routes

A

hep B

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15
Q

transmitted through parenteral route

A

hep C, hep D

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16
Q

viruses that can cause chronic liver disease

A

hep C > 80%

hep B = 10%

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17
Q

hep virus diagnosed via PCR

A

hep C

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18
Q

hep virus diagnosed by presence of surface antigen or antibody to core antigen

A

hep B

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19
Q

what percent of patients who develop cirrhosis secondary to hep C go on to die?

A

50%

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20
Q

major cause of chronic liver disease WORLDWIDE

21
Q

areas with highest prevalence of chronic HBV

A

northern canada, alaska, northern amazon, africa, SE asia

22
Q

what percent of patients infected with HBV go on to develop chronic hepatitis?

23
Q

presence of serum HBeAg, HBV-DNA and IgM anti-HBc would signify:

A

acute, active HBV infection

24
Q

presence of serum IgG anti-HBs and IgG anti-HBc

A

chronic HBV infection

25
effect of hep D coinfection with HBV
potentiates effects of HBV --> increased risk of fulminant hepatitis, faster progression to end-stage liver disease
26
woman presents with a history of other autoimmune diseases
autoimmune hepatitis
27
serology of autoimmune hepatitis
autoantibodies (ANA, ASMA, anti-LKMB), elevated IgG
28
plasma cell-rich chronic hepatitis
autoimmune hepatitis
29
middle-aged woman presents with pruritus, jaundice; elevated alk phos, GGT, bilirubin
primary biliary cirrhosis
30
serology of primary biliary cirrhosis
anti-mitochondrial antibody, elevated IgM
31
prognosis of primary biliary cirrhosis
25% with liver failure in 10y
32
patient presents with progressive fatigue, pruritus and jaundice. elevated alk phos. history of ulcerative colitis
primary sclerosing cholangitis
33
diagnosis of primary sclerosing cholangitis
cholangiography --> stenosis of ducts
34
histology: periductal "onion skin" fibrosis
primary sclerosing cholangitis
35
what lobule zone is affected by acetaminophen toxicity
zone 3 = centrilobular necrosis
36
causes of hepatic steatosis
metabolic syndrome (T2DM), alcohol, drugs, Wilson disease, viral infection
37
mechanism of steatosis
lipid influx > lipid clearance
38
steatosis with associated hepatocellular injury
steatohepatitis
39
mechanism of alcohol steatosis/steatohepatitis
increased liplysis and de novo lipogensis from carbs; blocked B oxidation and VLDL generation
40
histology: neutrophilic infiltrates, Mallory bodies
alcohol steatosis
41
genetic iron overload disease, throughout the body --> liver disease, diabetes, heart failure
hereditary hemochromatosis
42
hereditary hemochromatosis genetics
autosomal recessive HFE gene mutations (C282Y and H63D) --> abnormal regulation of Fe absorption
43
genetic copper overload throughout the body --> liver disease, neuropsych sx
Wilson disease
44
Wilson disease genetics
autosomal recessive mutation in ATP7B gene --> disrupted bile excretion of copper
45
autosomal recessive disease that most often presents with pulmonary emphysema, but can also involve liver disease
a1-antitrypsin deficiency
46
normal/abnormal genotypes for alpha-1-antitrypsin
``` normal = PiMM abnormal = PiZZ ```
47
histology: PASD stain --> pink globules
alpha-1-antitrypsin deficiency
48
malignant liver masses in adults
hepatocellular carcinoma, cholangiocarcinoma
49
benign liver masses in adults
hemangioma, focal nodular hyperplasia, hepatocellular adenoma