Exam 2 - Liver And Pancreas Flashcards

1
Q

Increased levels of bilirubin cause

A

Jaundice (icterus)

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2
Q

Serum bilirubin levels are abnormal when they exceed _____ however skin discoloration is not apparent until _____

A

Excess serum bilirubin level: 1.2 mg/dl

Skin discoloration: 2-3 mg/dl

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3
Q

How much bilirubin is formed daily?

A

250-350 mg

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4
Q

Within the hepatocyte, billirubin is…

A
  1. Conjugated with glucuronide to form billirubine diglucuronide secreted in bile
  2. This post-hepatic or conjugated billirubin is water-soluble and enters urine when serum levels are atypically high
  3. Billirubin in bile reaches intestines and is acted upon by bacteria to form stercobilin, a pigment of stool
  4. Portions of urobilin are absorped by intestines and after reaching circulation, some of this appears as urinary urobilin (urobilinogen)
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5
Q

Indirect vs direct bilirubin

A

Indirect: unconjugated, prehepatic
Direct: conjugated, posthepatic

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6
Q

Is prehepatic or posthepatic bilirubin insoluble in water?

A

Prehepatic bilirubin = unconjugated

Note: Posthepatic / conjugated bilirubin is water soluble and so it DOES appear in urine.

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7
Q

Obstructive jaundice (cholestasis) is caused by what?

A

Biliary obstruction

So bile “spills over” into tissue. Components are absorbed by circulation. Accumulated bilirubin is predominantly conjugated.

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8
Q

Jaundice associated with liver damage or dysfunction is often known as

A

Hepatic (hepatomegaly-cellular) jaundice

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9
Q

Causes of Hepatic (hepatomegaly-cellular) jaundice include

A

Cirrhosis, hepatitis, liver infarcts, toxic injury and defects in assimilation, conjugation and transport of bilirubin into bile

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10
Q

Atypically high conjugated bilirubin leads to a type of jaundice called

A

Choluric jaundice

Diffuses freely into blood and tissue fluids

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11
Q

Why are newborns often jaundice?

A

The hepatic mechanisms for conjugating and excreting often do not mature until about 2 weeks of age.

Mild unconjugated hyperbilirubinemia is frequent in young infarcts, especially premature and underweight.

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12
Q

Kernicterus

A

Infantile severe unconjugated hyperbilirubinemia with brain damage

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13
Q

What kind of bilirubin DOES enter the urine

A

Conjugated bilirubin

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14
Q

Acholuric jaundice

A

Unconjugated bilirubin that does not enter urine

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15
Q

3 Stages of cirrhosis

A

1- Fatty liver stage (fatty metamorphosis)
2- Alcoholic hepatitis
3- Cirrhosis (fibrosis) “end stage”

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16
Q

Mallory bodies are seen in which stage of liver disease

A

Alcoholic hepatitis

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17
Q

Biliary cirrhosis

A

Most damage occurs in periportal areas that surround bile ducts

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18
Q

“Pigment” cirrhosis is associated with

A

Hemachromatosis “bronze diabetes”

Accumulated iron and injury to hepatocytes and hepatic scarring

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19
Q

Hemosiderin

A

Insoluble aggregates consisting of degraded ferritin

Deposits are common in macrophages of the liver, spleen and marrow and hepatocytes

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20
Q

Systemic iron overload

A

Deposits accumulate and damage parenchymal tissues.

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21
Q

Causes of systemic iron overload:

A

Unregulated intestinal absorption, hemolytic anemia, multiple transfusions

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22
Q

Hemochromatosis “bronze diabetes” triad

A

Cirrhosis
Pancreatic fibrosis
Bronzed skin

(Also causes atypical arthritis)

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23
Q

What is the primary reason for hemochromatosis

A

Defect in chromosome 6 that affects regulation of intestinal absorption of iron

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24
Q

Secondary hemochromatosis may result from

A

Chronic hemolytic disorders and/or multiple transfusions

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25
What is characterized by increased tissue iron generally limited to the macrophages with little effect on parenchyma
Hemosiderosis | Versus hemochromatosis which is asssociated with damaging parenchymal tissue deposits
26
Treatment (2) of hemochromatosis
Phlebotomy | Dietary restriction of iron
27
Hepatolenticular degeneration
Wilson’s disease
28
What condition is associated with disturbances in regulation of copper transport and excretion into bile
Wilson’s disease
29
In Wilson’s disease, copper accumulates in (4)
Liver, brain, eyes, kidneys
30
In Wilson’s disease, copper is deposited where in the eye and what is this called
Cornea-sclera junction; Kaiser Fleischer ring
31
Cholelithiasis (lith = stone)
Gall stones
32
4F risks of cholelithiasis
Female Fat Forty (older than) Fertile (And the 5th is Flatulence)
33
What are contributing factors of abnormal bile?
Hypercholesterolemia Inadequate levels of bile acids Hemolytic disease with hyperbilirubinemia
34
How does Hypercholesterolemia contribute to abnormal bile?
Causes chemical injury to gall bladder mucosa Cholesterol absorbed by gall bladder diminishes motility of musculature and gives rise to “sluggish” gall bladder
35
Nucleation is promoted by increased
Mucin
36
Kidney stones vs Gall stones
Kidney stones = calcium | Gall stones = cholesterol
37
What are cholesterol stones
When the stone deposit is made up of 50% or more cholesterol
38
Pure stones
10% of all stones. Cholesterol (large, oval, small) and pigmented
39
How common are “Mixed” and “combined” stones?
80-90%
40
Cholecystitis
Inflammation of gall bladder
41
Majority of Cholecystitis is associated with
cholelithiasis (gall stones) 80-90% of the time
42
What contributes to chemical injury to bladder mucosa?
Hyperconcentrated bile
43
What enteric organisms are a concern with bacterial infection
E.coli and other organisms may enter gall bladder
44
What is the role in pathogenesis of pancreatic reflux?
Uncertain. When it occurs, mixing of the pancreatic secretions with bile may contribute to mucosal injury by activation of pancreatic enzymes.
45
When is bacteria present, in acute or chronic cholecystitis?
Acute cholecystitis (80% of the time vs 30% of the time with chronic)
46
Presentation/symptoms of acute cholecystitis
Enlarged, edematous and hyperemia (red) Steady, progressive right upper quadrant or epigastric pain and tenderness with fever, leukocytosis and nausea
47
Morphology of chronic cholecystitis
Gall bladder is often fibrotic and reduced in size.
48
In some chronic cholecystitis cases the gall bladder may be distended (_______)
Mucocele, “hydrops”
49
In chronic cholecystitis, calcified gallbladders is known as
“Porcelain gall bladder”
50
Symptoms of chronic cholecystitis
Right epigastric pain, nausea, intolerance of fatty foods
51
What is a first sign of liver tumor
Hepatomegaly
52
Most common cause for enlarged liver
Fatty liver caused by poor diet, obesity, alcohol, OTC meds (because liver processes)
53
Causes of hepatocarcinoma
- Hepatitis B (HPB) - Aflatoxin (peanuts) - Cirrhosis
54
Primary malignant tumors of the liver 93)
1- Hepatocarcinoma 2- Cholangiocarcinoma (of bile ducts) 3- Hemangiosarcoma (vascular)
55
Crohn’s, cystic fibrosis, (some) parasites, exposure to chemical agents can all lead to what primary malignant liver tumor
Cholangiocarcinoma (of bile ducts)
56
Gall bladder causes how many deaths per year?
5,000
57
What are symptoms of malignant gall bladder tumors?
Resembles cholecystitis and cholelithiasis: not much happens. Diagnosis is 1% for 5 year survival
58
Pancreatitis: what is it and what are some causes of it
Inflammation of pancreas Caused by infection, trauma, ischemia, drugs, hyperthermia, secretory obstruction, etc
59
Acute pancreatitis is associated with
Enzyme activation within pancreas that contributes to “auto digestion”
60
What are symptoms of acute pancreatitis
Sudden pain “acute abdomen” It’s the reason for about 1/500 emergency room admissions
61
Mild acute pancreatitis vs severe acute hemorrhagic pancreatitis
Mild: self-limiting Severe: extensive damage and possible death
62
Severe pancreatitis is also called
Acute hemorrhagic pancreatitis
63
Pathogenesis of severe (acute hemorrhagic) pancreatitis
Normally, pancreatic enzymes are activated in the gut and do not injure the pancreas. In acute pancreatitis, activation of trypsin may be a key step since it has the capacity to activate other enzymes (elastases, collagenases, phospholipidase, etc.) and the kinin system within the pancreas.
64
Causes of severe acute pancreatitis
Chronic biliary disease and chronic alcohol abuse
65
Symptoms of severe acute pancreatitis
Sudden, intense, CONSTANT pain
66
Sudden, intense, constant pain that refers to upper back and usually follows meal or alcohol ingestion
Severe (acute hemorrhagic) pancreatitis
67
What is more common: chronic or acute pancreatitis
Chronic
68
What kind of pancreatitis occurs after multiple episodes that contribute to fibrosis, parenchymal atrophy and ultimately, pancreatic failuter
Chronic (relapsing) pancreatitis
69
Pancreatic carcinoma symptoms
Vague and mild early on.
70
What cell type is pancreatic carcinoma
Duct cell
71
Risk factors of pancreatic carcinoma
Smoking, diet, chemicals, more frequent in African-Americans and diabetics
72
When pancreatic carcinoma is located in pancreatic head, obstructive jaundice is likely. This may be associated with
Courvoisier’s “sign”
73
About 10% of obstructive jaundice is likely exhibit increased tendency for spontaneous (migratory) thrombosis which is associated with
Trousseau’s sign
74
What are two islet cell tumors?
1 - Beta cell tumors (insulinomas) | 2 - Gastrin-producing tumors (gastrinomas)
75
What kind of islet cell tumor might cause hypoglycemia
Beta cell tumor
76
What kind of islet cell tumor includes a classic “triad” and is the second most common form of islet tumor?
Gastrin-producing tumors
77
What is the classic “triad” of gastrin-producing tumors and what is it known as
Zollinger Ellison syndrome 1 - gastrin producing islet cell tumor 2 - gastric hyperaciditiy 3 - intractable multiple peptic ulcers (stomach, duodenum, esophagus, jejunum)
78
Type I IDDM
Insulin dependent diabetes mellitus “juvenile onset”
79
Type II NIDDM
Non-insulin independent diabetes myelitis “adult onset”
80
Secondary contributing factors to diabetes mellitus
Inflammatory, surgical, neoplasticism or other conditions that damage islet tissue. Dysfunction of pituitary or suprarenal glands, certain drugs, etc.
81
When do chronic lesions appear in Type I and Type II Diabetes?
10-15 years
82
Glomerular sclerosis
Nephropathy
83
DM causes ___% legal blindness in US
15%
84
What is a common lesion of the eyes that is associated with disease of retinal vessels with exudation, fibroproliferative responses, microaneurysms, hemorrhages
Retinopathy
85
DM is most common metabolic cause for
Peripheral neuropathy
86
Is Peripheral neuropathy unilateralal or bilateral
Bilateral. Because its systemic disease
87
Type I diabetes and the 3 Ps
Polyuria Polydipsia Polyphagia