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
Causes of unconjugated hyperbilirubinemia in neonates
1. Physiologic jaundice of the newborn 2. Hemolytic disease 3. Breastmilk hyperbilirubinemia
26
* Bilirubin concentrations peak within 3-5 days of birth and remain elevated for less than 2 weeks * Bilirubin conc. = < 5 mg/dl; 90% unconjugated
Physiologic jaundice of the newborn
27
results from maternal-fetal incompatibility of Rhesus blood factors
Hemolytic disease
28
Infant becomes jaundiced with unconjugated bilirubin in the 1st or 2nd day of life and is susceptible to kernicterus
Hemolytic disease
29
Affects about 30% of breast-fed newborns due to alpha-glucuronidase in breast milk
Breastmilk hyperbilirubinemia
30
Hyperbilirubinemia where conjugated bilirubin exceeds 1.5 mg/dl
Conjugated hyperbilirubinemia
31
Major acute liver diseases
1. Acute hepatitis | 2. Cholestasis
32
Long-term complications of chronic hepatitis
1. Cirrhosis | 2. Hepatocellular carcinoma
33
Hepatocyte injury leads to
Hepatocellular disease
34
Biliary cell injury leads to
Cholestasis