P1.2-LIVER FUNCTION ALTERATIONS Flashcards

1
Q

Yellow discoloration of the skin, eyes, and mucous membranes

A

jaundice

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

At what bilirubin levels does overt jaundice become noticeable?

A

When bilirubin levels reach 3.0-5.0 mg/dL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the three classifications of jaundice

A

Prehepatic, hepatic, and posthepatic jaundice

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Where do abnormalities reside in prehepatic and posthepatic jaundice?

A

Outside the liver

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

An abnormality that occurs before liver metabolism, leading to unconjugated hyperbilirubinemia.

A

prehepatic jaundice

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are common causes of prehepatic jaundice?

A

Acute and chronic hemolytic anemias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What lab result is typical for prehepatic jaundice

A

Elevated unconjugated bilirubin (B1).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Jaundice caused by intrinsic liver defects affecting bilirubin metabolism or transport.

A

hepatic jaundice

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

A conjugation deficit where B1 cannot be converted to B2

A

Crigler-Najjar syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the types of Crigler-Najjar syndrome?

A

Type 1 (complete absence of enzymatic conjugation) and

Type 2 (severe enzyme deficiency).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What lab result is typical for Crigler-Najjar syndrome?

A

Elevated unconjugated bilirubin (B1).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

A genetic mutation in the UGT1A1 gene affecting bilirubin conjugation.

A

Gilbert’s syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What lab result is typical for Gilbert’s syndrome

A

Elevated unconjugated bilirubin (B1).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

A bilirubin excretion deficit due to a deficiency in the canalicular multidrug resistance protein

A

Dubin-Johnson syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What lab result is typical for Dubin-Johnson syndrome

A

Elevated conjugated bilirubin (B2).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How does Rotor syndrome differ from Dubin-Johnson syndrome?

A

Rotor syndrome lacks the dark pigmented granules seen in liver biopsies of Dubin-Johnson syndrome.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Jaundice due to a deficiency in the enzyme UDPGT, leading to elevated unconjugated bilirubin (B1).

A

physiologic jaundice of the newborn

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the treatment for physiologic jaundice of the newborn?

A

Ultraviolet radiation (phototherapy).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

A form of unconjugated hyperbilirubinemia caused by an inhibitor of bilirubin conjugation.

A

Lucey-Driscoll syndrome

20
Q

What lab result is typical for Lucey-Driscoll syndrome?

A

Elevated unconjugated bilirubin (B1).

21
Q

What causes posthepatic jaundice?

A

Biliary obstructive diseases, such as gallstones or tumors, preventing the flow of conjugated bilirubin.

22
Q

What is a common symptom of posthepatic jaundice?

A

Clay-colored stools.

23
Q

A condition where scar tissue replaces normal liver tissue.

24
Q

What are early signs of cirrhosis?

A

Often asymptomatic in early stages; symptoms appear as liver function deteriorates.

25
What is the most common cause of cirrhosis in the US?
Chronic alcoholism
26
What are other causes of cirrhosis?
Chronic hepatitis B, C, and D, autoimmune hepatitis, inherited disorders, nonalcoholic steatohepatitis, blocked bile ducts, drugs, toxins, and infections.
27
A disorder characterized by copper accumulation in the liver and other organs, potentially leading to cirrhosis.
Wilson Disease
28
A condition of iron overload, with excess iron accumulating in the liver.
hemochromatosis
29
An inborn error of carbohydrate metabolism that can lead to cirrhosis.
galactosemia
30
How is cirrhosis treated?
Abstaining from alcohol and medications for hepatitis-related cirrhosis.
31
Tumors that begin in liver cells.
primary liver tumors
32
Tumors from other body parts that spread to the liver, more common than primary tumors.
metastatic liver tumors
33
What is the most common primary malignant liver tumor
Hepatocellular carcinoma
34
A disorder associated with elevated ammonia, often following a viral infection, mostly in children.
Reye syndrome
35
What is a key epidemiological factor for Reye syndrome?
Ingestion of aspirin during a viral illness
36
What lab results are typical in Reye syndrome
Mild hyperbilirubinemia, elevated ammonia, and elevated aminotransferases (AST and ALT).
37
What causes drug-induced liver injuries?
Drugs, with alcohol being the most common cause
38
How does alcohol cause hepatic toxicity?
Through metabolism in the liver involving alcohol dehydrogenase and aldehyde dehydrogenase.
39
What are the stages of alcohol-related liver damage?
Alcoholic fatty liver, alcoholic hepatitis, and alcoholic cirrhosis.
40
What lab results are typical in alcoholic hepatitis?
Elevated AST, ALT, GGT, ALP, total bilirubin (>30 mg/dL), decreased serum albumin, prolonged PT.
41
What is the definitive diagnosis method for alcoholic cirrhosis?
Liver biopsy
42
Inflammation of liver tissue, often due to viral infections.
hepatitis
43
What are the common viral subtypes causing hepatitis?
HAV, HBV, HCV, HDV, and HEV
44
How are HAV and HEV transmitted?
Fecal-oral route.
45
How are HBV, HCV, and HDV transmitted
Parenteral and sexual routes
46
What symptoms are common in hepatitis?
Jaundice, dark urine, fatigue, nausea, vomiting, and abdominal pain.
47
What indicates chronic hepatitis in HBV and HCV?
Prolonged elevation of serum transaminase levels for longer than 6 months