Lecture 7.2 Highlights Flashcards

* = also MJ slide

1
Q

Chronic liver failure: Hepatorenal syndrome
1) Systemic vasodilation → decreased systemic vascular resistance, which causes _______________ to decrease
2) What does this cause?

(side note: if you see an out of place * on any of these slides, it’s also an MJ/ mick jagger slide, so extra important)

A

1) renal perfusion ↓
2) → ↓UOP & ↑BUN/Cr

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2
Q

Acute liver failure: Hepatic Encephalopathy
1) Has a range of neuro symptoms, often see ___________
2) Also see ↑ _____________ levels

A

1) asterixis
2) ammonia

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3
Q

*Define net effect

A

Accumulation of intracellular lipids

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4
Q

*Alcoholic hepatitis (10-35%):
1) Acetaldehyde (metabolite of ETOH) disrupts _____________ and _____________ function.
2) ETOH affects what two things?
3) What damages membranes and proteins in this condition?

A

1) cytoskeleton and membrane function
2) Mitochondrial function and membrane fluidity
3) ROS, generated during oxidation of ETOH

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5
Q

NAFLD may show all the changes associated with alcoholic liver disease; list 3

*Nonalcoholic Fatty Liver Disease

A

1) Steatosis
2) Nonalcoholic steatohepatitis (NASH)
3) Cirrhosis

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6
Q

Drug & Toxin-Induced Liver Injury: What are the 2 types? Give examples of each

A

1) Predictable (intrinsic): Acetaminophen
2) Unpredictable (idiosyncratic): Chlorpromazine + Halothane

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7
Q

Acetaminophen is a classic example of what type of liver injury?

“definitely know”

A

Predictable (intrinsic)

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8
Q

Hemochromatosis causes Hepatic Injury (after 20 g of stored Fe accumulated) through what 3 mechanisms?

A

1) Lipid peroxidation
2) Collagen formation after activation of stellate cells
3) DNA damage by ROS

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9
Q

*Wilson Disease pathogenesis:
1) What is the inheritance pattern?
2) What decreases? What is there a failure of?
3) What is there a secondary accumulation of as a result?

A

1) Autosomal recessive mutation in ARP7B gene
2) ↓ copper excretion into the bile and failure to incorporate copper into ceruloplasmin
3) Toxic levels of copper in tissues and organs

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10
Q
  • Wilson disease clinical manifestations:
    1) What organ takes the brunt of it? What are the 2 ways it can present?
    2) What causes the potential Neuropsychiatric complications?
    3) What is a common Sx?
A

1) Liver takes the brunt, may present as acute or chronic liver disease
2) Copper in basal ganglia
3) Kayser Fleischer rings

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11
Q

*α1-Anti-Trypsin Disease causes liver injury because of what?

“should know”

A

Hepatocellular build up of misfolded α1AT

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12
Q

Hepatic bile serves 2 functions, which are what?

A

1) Emulsification of intra-luminal fat via detergent action of bile salts
2) Elimination of bilirubin, cholesterol, xenobiotics, and other waste not removed from urine

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13
Q

There are 3 ways to disturb the equilibrium between bilirubin production and clearance.
List them and give an example of each.

A

1) Increased bilirubin production (e.g. extravascular hemolysis)
2) Hepatocyte dysfunction (e.g. hepatitis)
3) Obstruction of bile (e.g. impacted gallstone)

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14
Q

Predominately unconjugated hyperbilirubinemia:
1) What is a Sx of excess production of bilirubin?
2) What are at least 2 conditions of impaired bilirubin conjugation?

A

1) Hemolytic anemias
2) Physiologic jaundice of the newborn
-Diffuse hepatocellular disease (ex: viral/ drug induced hepatitis, cirrhosis, etc)

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15
Q

Predominately conjugated hyperbilirubinemia: List 2 causes

A

1) Decreased hepatocellular excretion
2) Impaired intra/extraheptic bile flow

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16
Q

Predominately conjugated hyperbilirubinemia:
Give 3 examples of causes of Impaired intra/extrahepatic bile flow

A

1) Primary biliary cirrhosis
2) Primary sclerosing cholangitis

3) Gallstones

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17
Q

What are the causes of cholestasis? List the 2 types and the subtypes

A

1) Obstruction of bile channels
a) Intrahepatic or extrahepatic
b) Inflammatory or mechanical
2) Defects in hepatocyte bile excretion

18
Q

What would be the lab findings in Cholestasis? (hint: 2 things increase)

A

↑ alk phos & ↑ GGT
(enzymes present in membranes of hepatocytes and cholangiocytes; they help make bile)

19
Q

List 2 kinds of Autoimmune Cholangiopathies

A

1) Primary Biliary Cholangitis
2) Primary Sclerosing Cholangitis

20
Q

Non-spurrative, inflammatory destruction of ________________ intrahepatic bile ducts occurs in Primary Biliary Cholangitis

A

small & medium-sized

21
Q

Cirrhosis Causes: What is the mnemonic to remember these? What are they?

A

VW’s Happen
Virus (hepatitis)
Wilson’s
Hemochromatosis
Alpha-1
PSC
PBC
Etoh
NASH

22
Q

What is the main reason to have your gallbladder removed?

A

Acute Calculous Cholecystitis (most common)

23
Q

In what circulatory disorder of the liver is there no direct damage to liver cells, so no aminotransferases?

A

Intestinal congestion

24
Q

Hepatocellular Adenoma (Benign):
1) What does it develop from?
2) What is a key aspect of the presentation?

A

1) Hepatocytes
2) Pain

25
Q

One cause of Hepatocellular Carcinoma (Malignant) (but not the main cause) is ________________; 90% develop in ___________ livers

A

Alcoholic Cirrhosis; cirrhotic

26
Q

What is the most common cause of Hepatocellular Carcinoma (Malignant)?

A

Chronic liver disease

27
Q

Cholangiosarcoma (Malignant) is a tumor involving intrahepatic or extrahepatic ______________

A

bile ducts

28
Q

1) Chronic inflammation & cholestasis are a risk factor for what malignant condition?
2) Give examples of chronic inflammations & cholestasis

A

1) Cholangiosarcoma (Malignant)
2) Primary sclerosing cholangitis
Hepatolithiasis
Fibropolycystic liver disease
Hep B & C
NAFLD

29
Q

Advanced age (>40), female, pregnancy, and obesity are are all risk factors for what condition that involves crystallization?

A

Cholesterol stones

30
Q

Acute Calculous Cholecystitis (most common) can be caused initially from chemical irritation and inflammation from __________________.

A

obstructed bile outflow

31
Q

List 4 important S/ Sx of Acute Calculous Cholecystitis

A

1) Biliary pain >6 hours
2) Leukocytosis
3) RUQ pain
4) US: gallstones

32
Q

Acute Calculous Cholecystitis could be complicated by a bacterial superinfection, leading to ____________ or ______________

A

cholangitis or sepsis

33
Q

Acute Calculous Cholecystitis is the most common reason for a ___________________

A

cholecystectomy

34
Q

*Things to remember: Cholangitis

(not actually highlighted, but emphasized in class)

A

1) Charcot’s Triad
-RUQ pain
Jaundice
Fever
2) Reynold’s Pentad (even worse)
-Hypotension
AMS

35
Q

*1) What is Charcot’s Triad?
2) What is it indicative of?

(not actually highlighted, but emphasized in class)

A

1) RUQ pain
Jaundice
Fever
2) Cholangitis

36
Q

1) What is the most important risk factor carcinoma of the gallbladder?
2) What is it likely secondary to?

A

1) Gallstones
2) Inflammation

37
Q

True or false: acute pancreatitis is an emergency

38
Q

Full blown acute pancreatitis is the result of what?

A

Systemic release of pancreatic enzymes and ↑↑↑ inflammatory response

39
Q

*Infiltrating ductal carcinoma is also called what?

A

“Pancreatic cancer”

40
Q

*What are typically silent until their extension impinges on some other structure?

A

Pancreatic carcinomas