34/36: Liver Pathology II - Carnevale Flashcards

(41 cards)

1
Q

presentation of primary biliary cirrhosis

A

pts present with fatigue and itching and progresses over 10-15 yrs presenting with progressive jaundice

pruritus
jaundice
steatorrhea
osteomalacia/osteoporosis
xanthomas
portal hypertension
hepatic failure
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2
Q

lab results primary biliary cirrhosis diagnosis

A

increased AMA, anti M2, IgM, AP5’NT/GGT, cholesterol

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3
Q

risk factors for primary sclerosing cholangitis

A

fibrous obliterative cholangitis
M>F
less than 50 yo
ulcerative colitis

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4
Q

s/s primary sclerosing cholangitis

A
jaundice
pruritus
WL
abdominal pain
cholangitis 
liver failure
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5
Q

lab results that diagnose primary sclerosing cholangitis

A
increase all of the following:
AP
GGt
5NT
ALT/AST
ANA, anti SMAb
pANCA
globulins

ERCP (endoscopic retrograde cholangiography shows beaded sclerosis)

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6
Q

complications of primary sclerosing cholangitis

A
chronic cholestasis
cholangitis
secondary biliary cirrhosis
liver failure
cholangiocarcinoma
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7
Q

condition in which the patients own immune system attacks the liver causing inflammation and liver cell death

A

autoimmune hepatitis

  • a chronic and progressive condition but may present acutely and be confused
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8
Q

autoantibodies: ANA, SMA, anti-LKM1

no viral markers, no AMA

increased globulines/IgG

A

autoimmune hepatitis

associated with other autoimmune disease as well

increase association with HLA DR4

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9
Q

which zone is affected by hepatic injury first?

A

zone 3 - centrilobular regions usually affected first because less oxygen here

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10
Q

phase I biotransformation is associated with… phase II is associated with

A

P450

glutathione S transferase
glucuronyl transferase

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11
Q

drug-induced liver disease morphology

tetracycline
methotextrate
acetaminophen
isoniazid
 halothane
amiodarone
steroids
erythromycin
A
microsteatosis
macrosteatosis
necrosis
hepatitis
hepatitis
fibrosis  
clholestasis
cholestasis
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12
Q

alcoholic liver disease develops in man who consumes… and woman who consumes…

A

greater than 80 g/day (6 pack)

greater than 40 g/day

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13
Q

liver
fatty change
perivenular fibrosis

A

steatosis

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14
Q
liver
liver cell necrosis
inflammation
mallory bodies
fatty change
A

hepatitis

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15
Q

liver
fibrosis
hyperplastic nodules

A

cirrhosis

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16
Q

foal lytic necrosis
mallory bodies
megamitochondria

indicate…

A

alcoholic hepatitis

longer abuse will see central hyaline sclerosis or chicken wire fibrosis or bridging fibrosis

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17
Q

clinical s/s alcoholic steatohepatitis

A
fever
leukocytosis
jaundice
increased AST and ALT less than 500 IU/L
increased AP 

AST/ALT ratio greater than 2

18
Q

in the end stage alcoholic the proximate cases of death are…

A

hepatic coma
massive GI hemorrhage
infection
hepatorenal syndrome following a bout of alcoholic hepatitis

19
Q

nonalcoholic steatohepatitis NASH causes (3)

A

insulin related/metabolic syndrome
drug hepatoxicity
pregnancy

20
Q

inherited disorder that increases the amount of iron that the body absorbs from the gut

A

hereditary hemochromatosis

most cases are caused by mutations in the HFE gene

21
Q

lab results hereditary hemochromatosis

A
increased 
serum Fe greater than 300 mg/dL
transferrin saturation greater than 2X
serum ferritin 2X
hepatic Fe index greater than 2
22
Q

if transferrin saturation and ferritin concentrations are high…

A

genetic testing for hemochromatosis is warranted

pt who are either homozygous for C282Y or heterozygous for C282y and H63D have hereditary hermochromatosis

23
Q

complications of hemochromatosis

A
hypopituitarism
skin pigmentation
cardiac failure
hepatocellular carcinoma
cirrhosis
diabetes
arthropathy
testicular atrophy
24
Q

hereditary disease that causes the body to retain copper

A

wilson’s disease

pts have decreased ceruloplasmin and excessive deposition of copper

w/o tx can cause severe brain damage, liver failure and death

25
kaiser-fleischer rings =
wilson disease also see decreased serum ceruloplasmin less tahn 20 mg/dl and increased hepatic copper above 250 and increased urinary copper above 100
26
describe alpha antitrypsin defiicency
autosomal recessive primary liver metabolic diasea primary genetic liver diseas in children 2nd cause of liver transplantation in children
27
alpha-antitrypsin deficiency diagnosis
low serum alphaAT abnormal electrophoretic alpha AT liver biopsy
28
risks of liver cell adenomas
may rupture in pregnancy and may harbor hepatocellular carcinoma
29
risk factors hepatocellular carcinoma
``` cirrhosis alcoholism HBV, HCV hereditary hemochromatosis alphaAT deficiency ```
30
s/s hepatocellular carcinoma
``` painful hepatomegaly abdominal mass weight loss portal/hepatic vein thrombosis hemorrhagic ascites heaptic failure massive bleeding ```
31
AFP above what is diagnositc of hepatocellular carcinoma>
1000
32
malignant primary tumor of the bile duct epithelium
cholangiocarcinoma
33
risk factors for cholangiocarcinoma
primary sclerosing cholangitis thorotrast liver flukes
34
*** most common malignant tumor of the liver
metastatic tumors common primary sites are GI tract, breast, lung, pancreas, and melanoma
35
three types of gallstones
``` cholesterol stones (biliary hypersecretion of cholesterol/supersaturation o f bile with cholesterol) pigmented stones ( bilirubin calcium salts) mixed ```
36
four contributing factors for cholelithiasis
supersaturation gallbladder hypmotility crystal nucleation accretion within the gallbladder mucous layer
37
usual microscopic appearance of chronic cholecystitis
collagen in wall (scarring) lymphocytes plasma cells macrophages
38
acute epigastric pain with radiation to the back
acute pancreatitis
39
laboratory findings of acute pancreatitis
elevation of serum amylase during first 24 hrs rising serum lipas levels w/i 72-96 hrs hypocalcemia may result from precipitation of calcium soaps in fat ecrosis -- poor prognosis
40
* clinical triad of chronic pancreatitis
diabetes steatorrhea calcifications along with permanent impairement of function and irreversible morphologic changes most commonly caused by alcohol ingestion
41
where do most carcinomas of pancreas arise?
head all arise from ductal epithelium