anatomy & functions Flashcards

(32 cards)

1
Q
  • Almost exclusively seen in children
  • Often preceded by a viral infection
  • Strong association with intake of Aspirin
  • Acute illness characterized by non-inflammatory encephalopathy and fatty degeneration of the liver
  • Mild hyperbilirubinemia; threefold changes in ammonia and aminotransferases (AST and ALT)
A

reye syndrome

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2
Q

The drug metabolizing system of the liver takes place mostly in the liver microsomes via the (?)

A

cytochrome P450 isoenzyme

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3
Q
  • Neonatal populations
  • Measurement of reflected light from the skin using 2 wavelengths, providing a numerical index based on spectral reflectance
  • Cannot be done in adult populations due to positive interference by carotinoid compounds
A

bilirubinometry

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4
Q

major waste product of heme catabolism

A

bilirubin

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5
Q

biliary obstructive disease, stool loses color (clay colored)

A

post hepatic jaundice

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6
Q
  • (?) to (?) kg
  • Extremely vascular - blood supply comes from the (?) and (?)
  • (?) ml blood/min

Functional unit : (?)
* Six - sided with one portal triad (comprised of a hepatic artery, a portal vein and a bile duct) on each side

  • Kupffer cells
  • Hepatocyte (80%)
A
  • 1.2, 1.5
  • hepatic aretry, portal vein
  • 1500
  • lobule
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7
Q
  • Used to detect hepatocellular damage
  • ALT - more liver specific and more greatly increased; highest increase in acute conditions
A

aminotransferases

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8
Q

lower prpduction of UDPGT due to genetic lesion and overall lower enzymatic activity; an additional defect related to a tranport deficit in the sinusoidal membrane of the hepatocyte may be present

A

gilbert disease

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9
Q

hypothesized to be due to a reduction in the concentration or activity of intracellular binding proteins; Liver biopsy does NOT show dark pigmented granules

A

rotor syndrome

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10
Q
  • infants whi are affected with crigler-najjar syndrome, especially the more sever form, develop severe (?), which typically leads to (?), the deposition of bilirubin in the brain.
  • the danger of kernicterus is a certainty at levels exceeding (?)
A
  • unconjugated hyperbilirubinemia
  • kernicterus
  • 20 mg/dl
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11
Q

tumors

  • (?) are more common than primary liver cancers
  • (?) is the most common malignant tumor of the liver
A
  • metastatic liver cancer
  • hepatocellular carcinoma
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12
Q
  • Clinical condition in which tissue scar replaces normal, healthy liver tissue
  • Most common causes include chronic alcoholism and chronic hepatitis C infection
A

cirrhosis

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13
Q

excellent marker of extrahepatic biliary obstruction

A

alkalin phosphatase

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14
Q

drug and alcohol-related disorders

  • (?) most commonly via immune mediated injury to the hepatocytes
  • (?) - most common drug which can cause liver damage; can lead to alcoholic cirrhosis
  • (?) can cause hepatic necrosis
A
  • drug cause injury
  • ethanol
  • acetaminophen
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15
Q
  • Third fraction of bilirubin
  • Conjugated bilirubin that is covalently bound to albumin
  • Seen only when there is significant hepatic obstruction
  • When present, will react in most laboratory method as conjugated bilirubin
A

delta bilirubin

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16
Q
  • bilirubin is very sensitive to and is destroyed by (?); therefore specimens should be protected from light
  • if left unprotected, bilirubin may reduce by (?)
A
  • light
  • 30-50% per hour
17
Q

jaundice

Increased amounts of bilirubin are being presented to the liver

A

prehepatic jaundice

18
Q

Jaundice becomes noticeable to the naked eye once bilirubin level reach (?) mg/dL.

19
Q

Almost all serum proteins are synthesized by the liver except (?) and (?)

A
  • immunoglobulins
  • vWF
20
Q

(?) are synthesized in the liver under normal circumstances when nutrition is adequate and the demand for glucose is being met. 70% of the daily production of cholesterol is produced by the (?).

21
Q

When carbohydrates are ingested and absorbed, the liver can do three thing;
* Use (?) for its own cellular energy requirements

  • Circulate (?) for use at the peripheral tissue
  • Store (?) at glycogen
22
Q

(?) not present in bone; used to differentiate ALP results; more sensitive to metastatic disease

A

5-nucleotidase

23
Q

more serious disorder; multiple mutations in the gene coding for UDPGT results in the production of midly dysfunctional to completely nonfunctional UDPGT

A

crigler-najjar syndrome

24
Q

jaundice

Primary problem is within the liver

A

hepatic jaundice

25
* removal of conjugated bilirubin from the liver cell and the excretion into the bile are defective * Caused by deficiency of the canalicular transporter protein (MDR2/cMOAT) * Appearance of dark-stained granules on a liver biopsy
dubin-johnson
26
premature neonates, deficiency of UPDGT
physiologic jaundice
27
* Also used to differentiate increased ALP results * Highest levels seen in biliary obstruction * Sensitive test for cholestasis caused by alcohol and drug ingestion
gamma-glutamyl transferase
28
every substance absorbed by the GIT must first pass through the liver
first pass phenomenon
29
Bilirubin + diazotized sulfanilic acid ---> (?)
azobilirubin
30
# conjugated or unconjugated * noncovalently attached to albumin * does not react woth the color reagent until the bilirubin is first dissociated from albumin using an accelerator (indirect) * nonpolar; water insoluble * aka hemobilirubin / slow-reacting bilirubin
unconjugated bilirubin
31
# conjugated or unconjugated * attached to one or two glucuronic acid molecules * reacys directly with the color reagent * polar;water soluble * aka cholebilirubin / one-minute / prompt bilirubin
conjugated bilirubin
32
Approximately (?) mg of bilirubin produced per day
200-300