Liver Pathology -Guo Flashcards

1
Q

True or False: Zone 3 is next to the central vein and is least supplied by oxygen and at risk for hypotension and congestion.

A

True

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2
Q

When can Hepatitis D infect?

A

with Hepatitis B

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3
Q

How is Hepatitis C graded?

A

biopsy!
-G0–> G3
need to determine inflammation and necrosis
-S1–> 3 for fibrosis (S2=portal septa, S3=bridging fibrosis)

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4
Q

How is autoimmune hepatitis diagnosed?

A
  • diagnosis of exclusion

- 70% women, 20-45 yo

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5
Q

What is the most common cause of cirrhosis in the Western world?

A

Alcohol

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6
Q

What histologic finding will be seen in Chronic Hepatitis B?

A

Ground glass hepatocytes

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7
Q

What histologic finding will be seen in Chronic Hepatitis C?

A

Portal tract lymphoid aggregates

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8
Q

What histologic finding will be seen in Autoimmune hepatitis?

A

interface hepatitis, plasma cell infiltrates, autoantibodies

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9
Q

What histologic finding will be seen in acute hepatitis?

A

inflammatory infiltrates and councilman bodies

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10
Q

What are the risk factors for hepatocellular carcinoma?

A
  • Chronic Hep B (»>) or Hep C virus
  • cirrhosis
  • smoking
  • higher risk in blacks
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11
Q

What populations of people get hepatocellular carcinoma?

A
  • 60yo with cirrhosis

- 20-40 yo without cirrhosis

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12
Q

What is the #3 most frequent cause of cancer related death?

A

Hepatocellular carcinoma

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13
Q

What is the typical presentation of fibrolamellar HCC?

A
  • male=female
  • young age (25)
  • normal AFP
  • good prognosis
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14
Q

What is the most common autosomal recessive genetic disorder?

A

Hemochromatosis –> causes the abnormal accumulation of iron in parenchymal organs –> organ toxicity

-secondary can be caused by disorders of erythropoiesis and treatment of diseases with blood transfusions

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15
Q

What is the most common genetic liver disorder in children and infants?

A

Alpha-1 antitrypsin deficiency

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16
Q

What are the pathologic features of PBC?

A
  • Early stage - portal/duct lesion
  • Periportal inflammation and injury
  • Ducts begin to disappear
  • Focal bile ductular proliferation
  • Cholestatic changes to periportal hepatocytes
  • Copper accumulation

-Fibrosis and eventually cirrhosis

17
Q

What do 80% of PSC (primary sclerosing cholangitis) pts have?

A

Ulcerative colitis

18
Q

What labs will be elevated with cholestasis?

A

ALP

NOT bilirubin