Wed Liver Pathology - AAW Flashcards

1
Q

First aid in brainscape - AAW GI

A

check it

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2
Q

primary biliary cirrhosis - what antibodies, what population

A

circulating antimitochondrial antibodies (AMA)

middle age female

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3
Q

itching - “hallmark” of what type of disease according to nelson

A

cholestasis

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4
Q

what do you see when you look at a bile canaliculus in someone with primary biliary cirrhosis

A

lymphocytic/granulomatous cholangitis

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5
Q

PBC vs alcoholic cirrhosis - what does the regeneration of the liver nodes look like in each

A

in PBC, the nodes are less round

alcoholic, they are more round

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6
Q

primary sclerosis cholangitis - 70% of cases are assc with what bowel thing.

average patient age/sex of that thing?

A

IBD, mostly ulcerative cholitis

male ~40 y/o

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7
Q

“cholestatic injury pattern” labs

A

elevated alkaline phosphatase and GGT (gamma-glutamyltransferase)

seen in primary sclerosing cholangitis and primary biliary cirrhosis

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8
Q

obliterative fibrosing cholangitis is “textbook” for what

A

primary sclerosing cholangitis

you can see a big fibrous plug next to an artery in the liver

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9
Q

hereditary hemochromatosis - defeciency in what

A

decreased synthesis of hepcidin

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10
Q

where does iron accumulate in the hepatocytes in early hemochromatosis

A

periportal region

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11
Q

secondary hemochromatosis - where does the iron initially accumulate

A

in the kupffer cells (contrasted with in the hepatocytes in primary)

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12
Q

best screening test for hemochromatosis

A

fasting transferrin saturation

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13
Q

diagnostic tests in wilsons

A

24 hr copper excretion (increased)

lack of ceruloplasmin causes overall low serum copper

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14
Q

what type of alpha 1 antitrypsin deficiency gives you the mostest liver disease

A

PiZZ

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15
Q

stain the liver for A1AT with……………………………

A

PAS ya goof

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16
Q

presence of obstructive, nonthrombotic lesions of the small (central) hepatic veins in patients exposed to radiation and/or hepatotoxins. marked narrowing and obliteration of central vein lumens by subendothelial swelling

called?
it patients who have had what done?

A

sinusoidal obstruction syndrome (hepatic veno-occlusive disease)

usually in BM transplant patients, chemo patients.

17
Q

prolonged conjugated hyperbilirubinemia in the neonate

A

neonatal cholestasis

due to:

biliary atresia: obstruction of lumen of extrahepatic biliary tree within first 3 months of life

neonatal hepatitis: due to A1AT, drugs, biliary atresia itself, etc.

18
Q

fatty, micronodular cirrhosis

what is wrong

A

this is the liver in early stages of alcoholic cirrhosis

19
Q

what type of steatosis is seen in reyes syndrome?

acute fatty liver of pregnancy? non-alcoholic fatty liver disease

A

microvesicular steatosis in reyes and AFLoP

macrovesicular in non-EtOH fatty liver

20
Q

AST:ALT ratio in alcoholic liver disease

A

greater than 2

80% of AST is found in mitochondria, and EtOH is a mitochondrial toxin

21
Q

ALP is high but you want to make sure its because of the liver and not something else

what do you test
what else would it be?

A

GGT

if GGT is negative, it could be bone instead of liver disease

22
Q

you WILL be tested on this

lab tests for

viral hep
autoimmune hep
wilsons
A!AT
hemochromatosis
primary biliary cirrhosis
A

viral hep - serology, nuclear testing (HBsAg, anti-HBc (total), HBV DNA, anti-HCV, HCV RNA)

autoimmune hep - ANA, anti-smooth muscle antibodies

wilson’s - ceruloplasmin

A1AT - A1AT level, phenotype

hemochromatosis - Fe, TIBC, Transferrin sat, genetics

primary biliary cirrhosis - anti-mitochondrial antibodies

23
Q

seen these on liver biopsy - what are you thinking

Ground glass hepatocytes
plasma cells
lymphocytic/granulomatous cholangitis
Fibrous obliterative cholangitis
periportal hepatitis with mild steatosis
globular hepatocyte inclusions
A

Ground glass hepatocytes - chronic viral hep B

plasma cells - autoimmune hep, primary biliary cirrhosis

lymphocytic/granulomatous cholangitis - primary biliary cirrhosis

Fibrous obliterative cholangitis - primary sclerosing cholangitis

periportal hepatitis with mild steatosis - chronic viral hepatitis C

globular hepatocyte inclusions - A1AT deficiency