Liver Pathologies (Exam 1) Flashcards

(40 cards)

1
Q

What are the most common causes of cirrhosis and fibrosis?

A

-long term alcohol abuse
-viral hep
-non-alcoholic fatty liver disease
-hemochromatosis
-autoimmune hepatitis
-primary biliary cholangitis
-primary sclerosing cholangitis
-wilson’s disease
-cystic fibrosis

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2
Q

What are the lab findings for liver cirrhosis and fibrosis?

A

-decreased albumin
-increased PT/INR
-potentially increased ammonia

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3
Q

What pathology is this?
-immune system attacks small bile ducts in the liver
-ducts become inflamed and narrowed
-causes obstruction to the flow of bile out of the liver and into intestines
-may lead to fibrosis and cirrhosis
-bile accumulation= increased synthesis of ALP

A

primary biliary cholangitis

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4
Q

What pathology has these lab findings?
-increased ALP during early stages*
-increased GGT, AST and ALT
-increased conjugated bilirubin
-bilirubinuria
-decreased albumin
-anti-mitochondrial Abs
-increased cholesterol in 50% of patients
*

Test q

A

primary biliary cholangitis

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5
Q

AAT deficiency is an inherited disorder. How is it inherited?

A

autosomal recessive

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6
Q

What pathology is this?
-lack of protease inhibitors causes an excess of protease enzymes from neutrophils
-protease enzymes attack the liver and lung tissue and cause liver cirrhosis and lung disease
-lung symptoms usually appear first

A

AAT deficiency

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7
Q

What pathology would have these S&S and lab findings?
-early onset emphysema (panacinar)
-SOB
-excessive cough with sputum production
-hemoptysis
-cirrhosis
-acute and chronic inflammation
-serum AAT will be decreased

A

AAT deficiency

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8
Q

What pathology is this?
-loss of liver function occurs rapidly usually in a person who has no pre-existing liver disease
-most commonly caused by hep virus or drugs such as acetaminophen
-increased liver enzymes
-increased ammonia

A

acute liver failure/ acute fulminant liver failure

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9
Q

What pathology is this?
-late development of liver failure and then eventually hepatic encephalopathy
-increased liver enzymes
-increased ammonia

A

chronic liver failure/ subfulminant liver failure

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10
Q

What are the other names for hemochromatosis?

A

bronze diabetes or iron overload disorder

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11
Q

What pathology is this?
-primary cause: genetic
-secondary: excessive iron in diet or repeated blood transfusions
-results in excessive total body iron and deposition of iron in tissues like skin, spleen, pancreas, heart, liver, thyroid, pituitary

A

hemochromatosis

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12
Q

What is the hemochromatosis triad?

A

1) cirrhosis
2) diabetes
3) skin pigmentation

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13
Q

What pathology has these lab findings?
-increased serum transferrin saturation
-increased serum ferritin
-HFE gene testing

A

hemochromatosis

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14
Q

What is another name for Wilson’s disease?

A

hepatolenticular disease

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15
Q

How is wilson’s disease inherited?

A

autosomal recessive

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16
Q

What pathology is this?
-copper build up in liver, brain, and eyes
-kayser fleischer rings around eye
-decreased serum ceruloplasmin (carrier for copper)
-increased 24 hour urine copper
-decreased or normal serum copper
-liver biopsy will show excess copper (gold standard)

A

wilson’s disease

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17
Q

What is the gold standard of diagnosis for wilson’s disease?

A

liver biopsy shows excess copper deposition

18
Q

What pathology is this?
-bile stasis due to hormonal changes
-intrahepatic cholestasis temporarily impairs liver function
-causes bile to build up in the liver and bloodstream
-intense pruritis during 2nd/3rd trimester, dark urine, and jaundice
-increased liver enzymes
-increased serum bile acid levels

A

cholestasis of pregnancy

19
Q

What pathology is this?
-decline in brain function that occurs because of severe liver disease
-liver cannot adequately remove toxins from blood
-causes a build up of toxins in bloodstream and can lead to brain damage
-liver failure leads to ammonia intoxication of the brain
-increased bilirubin
-decreased albumin
-increased ammonia

A

hepatic encephalopathy/ portosystemic encephalopathy

20
Q

What are the 6 F’s for gallstones?

A

female, fat, forty, fertile, fair, family hx

21
Q

stones/calculi in the gallbladder resulting from changes in bile components=

A

cholelithiasis

22
Q

chole=

A

bile containing

23
Q

docho=

24
Q

gallstones in the common bile duct obstructs bile flow is called

A

choledocholithiasis

25
Acute or chronic inflammation of gallbladder usually associated with impacted gallstones in the cystic duct causing painful distention =
cholecystitis
26
gallstone ulceration through gallbladder into the intestine and causes obstruction=
gallstone ileus
27
How are gallbladder disorders diagnosed?
HIDA scan or ultrasound
28
Steady gripping or gnawing pain in the RUQ near rib cage which can be serve and radiate to the upper back is known as murphy's sign. What does this sign indicate?
acute cholecystitis, or inflammation of the gallbladder
29
What are the 2 main functions of pancreas?
1) exocrine= help with digestion 2) endocrine= regulate blood sugar
30
What enzyme is this? -digestive enzyme that breaks down carbs -used to diagnose and monitor the clinical course of pancreatitis
serum amylase
31
increased serum amylase indicates?
pancreatitis or salivary gland disorders
32
decreased serum amylase indicates?
cystic fibrosis
33
What enzyme is this? -digestive enzyme that breaks down fat -used in the evaluation of pancreatic disease -more specific for pancreatitis than amylase**
serum lipase
34
increased serum lipase indicates?
pancreatitis!!!!!
35
decreased serum lipase indicates?
cystic fibrosis
36
What conditions can lead to pancreatitis?
-alcoholism -gallstones -cystic fibrosis ***gallstones and alcohol abuse are the leading causes*
37
What are the lab findings for pancreatitis?
increased amylase and lipase!!!! lipase is more specific*
38
What pathology is this? -genetic disorder that primarily affects the lungs, pancreas, and other organs by causing thick, sticky mucus to accumulate in these areas -caused by mutations in the CFTR gene (cystic fibrosis transmembrane conductance regulator), which disrupts chloride and water movement in cells, leading to abnormal mucous production -primarily considered a disorder in the exocrine glands: skin, digestive system, respiratory system, reproductive system -causes buildup of thick viscous mucus secretions in various organs -pancreatic insufficiency leading to malabsorption of fats and fat soluble vitamins (K,A,D,E) resulting in poor weight gain and steatorrhea (fatty stools) -large amounts of fatty, bulky foul smelling stool
cystic fibrosis/ fibrocystic disease of the pancreas
39
What is a common cause of death for someone with cystic fibrosis?
infection with pseudomonas aeruginosa
40
How is cystic fibrosis/ fibrocystic disease of the pancreas diagnosed?
-sweat test/ sweat chloride test (gold standard, will show increased level of chloride in sweat) -CFTR mutation analysis -chest xray