Liver disease Flashcards

1
Q

virtually all known acute/chronic hepatic injury patterns can results from drugs/toxins

A

yep

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2
Q

NAFLD may be morphologically indistinguishable from ALD

A

yep

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3
Q

histologic spectrum of NAFLD (3)

A
  1. simple steatosis
  2. steatohepatitis
  3. NASH and progressive fibrosis
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4
Q

mutations of genes encoding HFE

A

hereditary hemochromatosis

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5
Q

hereditary hemochromatosis

A

reduced synthesis/activity of hepcidin which results in uncontrolled small bowel Fe absorption

  • increased serum trnasferrin saturation
  • increased serum ferritin
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6
Q

hereditary hemochromatosis:

  1. symptoms appear in
    ____ decade
  2. classic triad
A
  1. 5th- 6th decade

2. classic triad: cirrhosis, diabetes, skin pigmentation

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7
Q

Wilsons

  1. inheritance pattern
  2. what is it
  3. mutation
  4. accumulation is
  5. increased/decreased serum ceruloplasmin
  6. complication
  7. treatment
A
  1. autosomal recessive
  2. deposition of copper
  3. encodes a transmembrane Cu-transporting ATPase on canalicular membrane
  4. it is toxic due to oxidative injury from free radicals formation
  5. decreased
  6. fulminant liver
  7. chelation
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8
Q

kayser-fleischer ring

A

wilson’s disease

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9
Q

chronic biliary diseases can progress to

A

cirrhosis

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10
Q

biliary tract diseases

  1. secondary
  2. primary
A
  1. secondary: extrahepatic biliary obstruction with gallstones, tumors or biliary atresia
  2. primary: autoimmune cholcangiopathies like PBC and PSC
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11
Q

primary biliary cholangitis/cirrhosis involves what part of the liver

A

intrahepatic bile ducts (autoimmune)

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12
Q

primary sclerosing cholangitis involves what part of the liver and is associated with

A

both intra and extra-hepatic bile ducts

  • IBD associated
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13
Q

non- suppurative granulomas cholangitis that results in florid duct lesion

A

primary bile cholangitis

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14
Q

primary bile cholangitis

  1. occurs in
  2. onset
  3. autoantibodies
  4. LFT
  5. treatment
  6. serology
A
  1. occurs in middle aged women
  2. insidious onset
  3. AMA ab (antimitochondrial)
  4. increased alk. phos
  5. UDCA
  6. positive AMA
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15
Q

localized aggregate of epithelioid macrophages that is either necrotizing or non-nectrotizing that is due to either an infectious cause such as mycobacteria or non-infectious causes like sarcoidosis

A

granulomatous hepatitis

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16
Q

primary sclerosing cholangitis:

  1. what is it
  2. occurs in
  3. association with
  4. diagnosis from
  5. increased risk of
  6. radiology
  7. serology
A
  1. autoimmune dysregulation of T-lymphocytes
  2. occurs in middle aged males
  3. association with IBD
  4. diagnosis from ERCP and MRCP
  5. increased risk of bile duct cholangiocarcinoma and GB and colon cancers
  6. strictures and beading of large bile ducts; pruning of smaller ducts
  7. positive ANCA
17
Q

benign neoplasm of hepatocytes that results in non-cirrhotic liver but may rupture and bleed. there is rare malignant transformation from a beta-catenin mutation

A

hepatocellular adenoma

18
Q

hyperplastic tumor-like growth of hepatocytes with nodular regenerative response to localized vascular perfusion abn.

A

focal nodular hyperplasia

19
Q

central stellate scar

A

focal nodular hyperplasia

20
Q

hepatic mass lesion resulting in a cirrhosis liver results in

A

HCC

21
Q

hepatic mass lesion resulting in a non- cirrhosis liver

  1. age<50
  2. age>50
A
  1. age<50: hepatocellular adenoma

2. age>50: metastases