Module 1 Unit 2: Liver Function Alterations Flashcards

1
Q

Jaundice comes from the French word _____ which means yellow

A

jaune

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2
Q

Yellow discoloration of the skin, eyes, and mucous membranes

A

Jaundice/Icterus

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3
Q

Common cause of jaundice

A

Retention of bilirubin

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4
Q

In adults, jaundice is noticeable if bilirubin levels reach

A

2-3 mg/dl

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5
Q

In neonates, jaundice is noticeable if bilirubin levels reach

A

5 mg/dl

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6
Q

Type of jaundice that occurs prior to liver metabolism

A

Pre-hepatic jaundice

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7
Q

Another term for pre-hepatic jaundice

A

Unconjugated Hyperbilirubinemia

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8
Q

TRUE or FALSE: Hepatic jaundice may result from ineffective erythropoiesis from the bone marrow resulting in premature death.

A

False; Pre-hepatic jaundice

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9
Q

Type of jaundice that results from an intrinsic liver disease

A

Hepatic jaundice

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10
Q

An inherited, autosomal recessive mild form of unconjugated hyperbilirubinemia where serum concentration of bilirubin ranges from 1.5-3 mg/dl

A

Gilbert Syndrome

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11
Q

Bilirubin is absent in urine and anemia does not occur

A

Gilbert Syndrome

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12
Q

This decreases bilirubin levels (bilirubin is measured in the FASTING STATE)

A

Phenobarbital

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13
Q

Patients with Gilbert Syndrome may be predisposed to

A

Acetaminophen toxicity

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14
Q

An inherited, autosomal recessive disorder caused by the complete absence of UDGPT

A

Crigler-Najjar Syndrome Type 1

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15
Q

In this disorder, serum bilirubin concentrations above 20 mg/dl are observed.
Most patients also die of severe brain damage due to kernicterus within the 1st year of life.

A

Crigler-Najjar Syndrome Type 1

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16
Q

An inherited, autosomal dominant disorder characterized by partial deficiency of UDPGT

A

Crigler-Najjar Syndrome Type 2

17
Q

In this disorder, serum bilirubin ranges between 5-20 mg/dl.

*Phenobarbital can correct this disorder.

A

Crigler-Najjar Syndrome Type 2

18
Q

A familial form of unconjugated hyperbilirubinemia due to the presence of a UDPGT inhibitor

A

Lucey-Driscoll Syndrome

19
Q

A rare autosomal recessive disorder characterized by jaundice with predominantly elevated conjugated bilirubin and a minor elevation of unconjugated bilirubin

A

Dubin-Johnson Syndrome

20
Q

The liver has a greenish-black appearance and dark brown pigment is seen in hepatocytes and Kupffer cells

A

Dubin-Johnson Syndrome

21
Q

A form of conjugated hyperbilirubinemia similar to Dubin-Johnson but WITHOUT liver pigmentation

A

Rotor Syndrome

22
Q

A neurologic syndrome that results in brain damage owing to the deposition of bilirubin in the brain

A

Kernicterus

23
Q

Poses an increased risk for the development of kernicterus, especially in low-birthweight infants

A

Unconjugated hyperbilirubinemia

24
Q

Frequent occurrence of jaundice in babies within a few days after birth

A

Physiologic jaundice of the newborn

25
Q

Causes of unconjugated hyperbilirubinemia in neonates

A
  1. Physiologic jaundice of the newborn
  2. Hemolytic disease
  3. Breastmilk hyperbilirubinemia
26
Q
  • Bilirubin concentrations peak within 3-5 days of birth and remain elevated for less than 2 weeks
  • Bilirubin conc. = < 5 mg/dl; 90% unconjugated
A

Physiologic jaundice of the newborn

27
Q

results from maternal-fetal incompatibility of Rhesus blood factors

A

Hemolytic disease

28
Q

Infant becomes jaundiced with unconjugated bilirubin in the 1st or 2nd day of life and is susceptible to kernicterus

A

Hemolytic disease

29
Q

Affects about 30% of breast-fed newborns due to alpha-glucuronidase in breast milk

A

Breastmilk hyperbilirubinemia

30
Q

Hyperbilirubinemia where conjugated bilirubin exceeds 1.5 mg/dl

A

Conjugated hyperbilirubinemia

31
Q

Major acute liver diseases

A
  1. Acute hepatitis

2. Cholestasis

32
Q

Long-term complications of chronic hepatitis

A
  1. Cirrhosis

2. Hepatocellular carcinoma

33
Q

Hepatocyte injury leads to

A

Hepatocellular disease

34
Q

Biliary cell injury leads to

A

Cholestasis