Liver Pathology Flashcards

(70 cards)

1
Q

What are the causes of cirrhosis?

A

etoh, viral hepatitis, biliary ds. hereditary hemochromatosis, wilsons ds. A1AT def, NAFLD

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2
Q

The 3 most common causes of death in cirrhosis?

A

hepatic failure
portal htn
hepatocellular carcinoma

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3
Q

List the some symptoms of hepatic failure

A

Jaundice, hypoalbunemia, bleeding, hyperammonemia, hypoglycemia, endocrine and renal failure, encephalopathy, pulmonary and portal htn

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4
Q

What is the most common cause of acute hepatic failure? Chronic?

A

acetaminophen OD

cirrhosis

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5
Q

Sinusoidal/central venous fibrosis, parenchymal nodules, arterial portal anastamoses adn hyperdynamic splanchnic circulation are all causes of what liver pathology?

A

Portal htn

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6
Q

Symptoms of portal htn?

A

ascites, splenomegaly, esophageal varices, hepatic encephalopathy

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7
Q

What would be seen on a liver biopsy fo a pt. with alcoholic steatosis?

A

enlarged lipid vacuoles

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8
Q

IF you see mallory bodies think this, yo.

A

Alcoholic hepatitis

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9
Q

What are the differences seen in imaging between early and late alcoholic cirrohsis?

A

Early- enlarged fatty liver w/micronodules

Late - shrunken, nonfatty, w/variable nodules

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10
Q

Causes of mortalitiy in alcoholic cirrhosis?

A
Hepatic encephalopathy
Esopahgeal varices
Infection
Hetaptorenal syndrome
Hepatocellular carcinoma
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11
Q

What is the diff between types of pt with non- alcoholic and alcoholic fatty liver disease?

A

Non-alcoholic - obese, T-II diabetes, dyslipidemia, and mucho insulin resistance
alcoholic - alcohol consumption

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12
Q

What is primary biliary cirrhosis?

A

inflammatory destruction of small and medium intrahepatic bile ducts

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13
Q

Dx tests for PBC?

A

ALP/GGT - elevated
AMA antibodies or (ANA and ASMA/AIH)
CD8+ T cells

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14
Q

What would a typical PBC look like and present as?

A

Middle age european female with pruritis, xanthelmsa/xanthoma, steatorrhea, osteomalacia/osteoporosis and other autoimmune ds.

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15
Q

Name causes of secondary billiary cirrhosis?

A

Stones, tumors, atresia, CFTR, choledocal cysts

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16
Q

What autoimmune disease is associated with PSC?

A

IBD - 70% of patients

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17
Q

What is the key finding for PSC?

A

Beaded cholangiogram and atypical p-ANCA

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18
Q

Describe Hereditary hemochromatosis.

A

AR decrease in hepcidin synth –> increased Iron absorption. Treated with phlebotomy and iron chelations. Also called bronze diabetes

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19
Q

What causes secondary hemochromatosis

A

parenteral overload
ineffective erythoproeisis
increased oral effective

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20
Q

Key difference in biopsy between hereditary and secondary hemochromatosis?

A

in hereditary iron in hepatocytes while in secondary it is in the Kupfer cells

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21
Q

what is the defect in Wilson’s disease?

A

AR defect in ATP7B- so you can secrete copper and ceruloplasmin into bile.

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22
Q

When would you suspect Wilson’s ds?

A

A teen with liver disease where all tests are coming up negative.

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23
Q

What would you see in a liver bx. in A1AT?

A

build up of A1AT in hepatocytes

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24
Q

Diagnosis of A1AT would involve what tests?

A

A1AT level, A1AT phenotype, liver bx. : PAS + cytoplasmic globular inclusions

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25
What is the difference between a direct and unpredictable cause of drug induced liver injury?
direct: all individuals sustain the same level of injury from the same dose unpredictable: level of damage is dependent on the individual
26
What are two causes of neonatal cholestasis?
biliary atresia and neonatal hepatitis
27
Describe neonatal hepatitis?
hepatitis caused by biliary atresia, A1AT inherited metabolic deficiency, tyrosinemia, CFTR, drug toxicity
28
What type of bilirubin accumulates in neonatal cholestasis?
conjugated
29
What are the causes of granulomatous hepatitis?
50% idiopathic, 20% Sarcoidosis, 5% drugs, 3% TB
30
Which liver enzyme is specific to hepatocellular damage?
ALT (alanine aminotransferase)
31
An AST:ALT >2 indicates what etiology of liver disease?
alcoholic
32
What are the liver function enzyme tests that would indicate a cholestatic etiology of liver disease?
ALP and GGT (ALP >>> ALT and AST)
33
If you see an increase in plasma cells on a liver bx., index of suspicion for what diseases are raised?
AIH and PBC (primary biliary cirrhosis)
34
Contrast the patterns seen on liver bx. for HBV and HCV
HBV- ground glass | HCV- periportal hepatitis and mild steatosis
35
What does grading of a liver bx. sample tell you?
the amount of fibrosis
36
When should you be concerned about Gilbert's syndrome?
Never, it is benign, may have icterus and elevated bilirubin during stressed times
37
What is acute cholangitis? What can cause it?
secondary bacterial infection of biliary tree, may be caused by hepatocellular cholestasis
38
Centrilobular fibrosis caused by cor pulomonale, hepatic vein thrombosis, CHF and shock is called this
Chronic passive congestion
39
radiation, BMT, chemo damage the hepatic sinusoidal endothelium causing lesions of small veins, narrowing of central veins
sinusoidal obstruction syndrome
40
Cardiac sclerosis is caused by these two liver vascular problems
Chronic passive congestion | centrilobular hemorrhaic necrosis
41
What is portal vein thrombosis caused by?
``` extrahepatic = trauma, intrabdominal sepsis, pancreatitis, hypercoaguable disorder intrahepatic = cirrhosis and carcinoma ```
42
Blood filled spaces in liver caused by anabolic steroid or bartonella infection?
Peliosis hepatitis
43
What causes acute massive hepatic necrosis? Likley outocomes?
acute hep., drug/toxin, vascular disease, AIH, Wilson's | Death or full recovery
44
Dx tools used for autoimmune hepatitis.
Type 1 - (ANA) (SMA) (anti-SLA/LP) | Type II - anti (ALKM-1), (ALC-1)
45
What does HELLP stand for?
hemolysis, eleveated liver enzymes, liver platelets
46
Dx sign of Acute fatty liver or pregnancy
microvesicalar steatosis
47
Intrahepatic cholestasis of pregnancy is caused by this normal effect of pregnancy
elevated estrogen
48
What are liver complications of a bone marrow transplant?
drug toxicity, sinusoidal obstruction syndrome, graft vs host ds
49
congenital dilation of the bile duct?
choledochal cyst
50
What disorders make up Caroli's disease?
Intrahpetiac dilations + congenital hep fibrosis
51
AR non-cirrhotic liver disease of kids?
Congenital hepatic fibrosis
52
What is nodular regenerative hyperplasia?
diffuse nonfibrosing nodular hyperplasia
53
Typical patient for hepatocellular adenoma?
young woman on oral estrogen contraceptions
54
What is the big concern with bile duct hamartoma?
nodules look like metastatic carcinoma
55
benign proliferation of bile ducts
bile duct adenoma
56
Describe the gross signs of HCC
solitary large mass or multiple nodules, soft, hemorrhagic
57
What is ironic about fibrolamellar variant of HCC?
Young patients with no cirrhosis or hepatitis. Also a firm lesion
58
what things increase risk of intrahepatic carcinoma (cholangiocarcinoma)
liver flukes, PSC, carolis ds, congential hepatic fibrosis, choledochal cyst, viral hep b/c, NAFLD
59
what is perihilar/klastkin tumor?
tumor at R/L hepatic duct confluence
60
Why is the prognosis for distal extrahepatic cholaniocarcinoma worse than most others?
it infiltrates into surrounding tissue
61
Describe cholesterol stones
water soluble, supersaturated bile, usually drugs cause these stones
62
common causes of pigment stones
bacterial and parasitic infection, disorders of hemolysis
63
Symptoms of acute cholecystitis
epigastric RUQ pain, leukocytosis
64
What condition is always present in chronic cholecystisit?
cholestatis
65
dystrophic calcification of the gallbladder wall is called this
porcelain glalbladder
66
describe cholesterolosis
accumulation of lipif laden macrophages (foamy) and yellow flecks
67
Mucocele/hydrops of the gallbladder involves this finding?
distended gallbladder with atrophic wall
68
This thickening of the gall bladders wall is not a true neoplasm.
Adenomyoma of the gallbladder
69
Why is gallbladder carcinoma so dangerous?
Often silent, already metastasized to liver at diagnosis.
70
this benign growth of the gall bladder can progress into adenocarcinoma
adenoma of gallbladder