DISEASES RELATED TO LIVER FUNCTION Flashcards

1
Q

Jaundice Comes from the word “_______” meaning __________

A

jaune - yellow

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2
Q

Characterized by the yellow discoloration of the skin,
mucous membrane, and sclera, most often because of _________

A

bilirubin

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3
Q

three types of jaundice

A

→ Prehepatic jaundice
→ Hepatic jaundice
→ Posthepatic jaundice

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4
Q

● Not synonymous with jaundice in the clinical laboratory setting

→ Refers to to serum or plasma with yellow discoloration due to
elevated bilirubin

A

Icterus

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5
Q

Excessive amount of bilirubin is presented to the liver for metabolism

A

PREHEPATIC JAUNDICE

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6
Q

↑ breakdown of RBCs

A

→ Hemolysis
→ Hemolytic anemia

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7
Q

breakdown of RBCs because of the parasite Plasmodium spp.

A

Malaria

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8
Q

→ Unconjugated hyperbilirubinemia

A

● Increased B1

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9
Q

● Impaired bilirubin excretion
● Elevated B2

A

B. POSTHEPATIC JAUNDICE

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10
Q

→ Biliary obstruction diseases of post hepatic jaundice

A

▪ Gallstones, tumor

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11
Q

● Result from impaired cellular uptake, defective conjugation, or
abnormal secretion of bilirubin by the liver cell(intrinsic liver
defect or or disease)

A

C. HEPATIC JAUNDICE

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12
Q

HEPATIC JAUNDICE
Unconjugated hyperbilirubinemia
→ ↑B1
1.
2.

● Conjugated hyperbilirubinemia
→ ↑B2
1.
2.

A

Unconjugated
1.Gilbert Syndrome
2. Crigler-Najjar Syndrome

Conjugated
1. Dubin-Johnson Syndrome
2. Rotor’s Syndrome

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13
Q

● Benign autosomal recessive hereditary disorder
● Genetic mutation of UGT1A1
● elevated B1

A

Gilbert Syndrome

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14
Q

→ In Gilbert Syndrome Liver is still functioning at ______ percent

A

30 %

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15
Q

● Gilbert syndrome may have no symptoms but with _________

A

mild icterus

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16
Q

It is more serious than Gilbert syndrome

A

Crigler-Najjar Syndrome

17
Q

It is characterized by deficiency of the enzyme UDPGT

A

Crigler-Najjar Syndrome

18
Q

What type?

Complete absence of UDPGT
− No conjugation of bilirubin

A

→ Type 1

19
Q

In Crigler-Najjar Syndrome the life expectancy is ________

A

<1yr

20
Q

What type?

Severe/partial deficiency of UDPGT

A

→ Type 2

21
Q

● Autosomal recessive disease which presents shortly after birth
with an increase of conjugated bilirubin without elevation of liver
enzymes (ALT, AST)

A

Dublin-Johnson Syndrome

22
Q

Deficiency in canalicular multidrug resistance/ multispecific
organic anionic transporter protein (MDR2/cMOAT)

A

Dubin-Johnson Syndrome

23
Q

AST and ALT in Dubin-Johnson Syndrome stands for?

A

Aspartate transaminase (AST)
Alanine transaminase (ALT)

24
Q

Defective excretion by the liver cell

A

Dublin-Johnson Syndrome

25
Q

Dubin-Johnson Syndrome
→ ____in the hepatocyte cannot easily transport into the bile
canal

A

B2

26
Q

Liver granules are not pigmented(liver biopsy)

A

Rotor’s Syndrome

27
Q

One test to differentiate Dublin-Johnson from
____________

A

Liver biopsy - Rotors syndrome

28
Q

● Same symptoms with Dubin-Johnson Syndrome

A

Rotor’s Syndrome

29
Q

● Increased ________ in Rotor’s syndrome

A

B2

30
Q

● Unknown etiology; ______________

A

Good prognosis - Rotor’s syndrome

31
Q

→ Neuronal degeneration

A

Kernicterus

32
Q

Give me at least 4 Physiological Jaundice of the Newborn

A

● Deficiency of UDPGT
→ results in the rapid buildup of unconjugated bilirubin, which
can be life threatening
● Kernicterus
→ Neuronal degeneration
● Cell damage and death in newborn
● Phototherapy (UV) or exchange transfusion (extreme case)

DKCP

33
Q

● Bilirubin-conjugation inhibition

A

Lucey-Driscoll Syndrome

34
Q

● Aka. Transient Familial Neonatal Hyperbilirubinemia

TFNH

A

Lucey-Driscoll Syndrome

35
Q

● Circulating inhibitor of bilirubin conjugation

A

Lucey-Driscoll Syndrome