Liver Pathology 2 Flashcards

1
Q

Fibrous deposition in alcoholic steatosis begins where in hepatocyte

A

around central vein

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2
Q

Non-alcoholic fatty liver disease/hepatic steatosis is most often due to

A

metabolic diseases
DM, hyperlipidemia, obesity
insulin resistance –> steatosis

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3
Q

Primary biliary cirrhosis

A

autoimmune destruction of intrahepatic bile ducts (extrahepatic bile ducts are spared)

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4
Q

AMA + disease

anti-mitochondrial antibody

A

primary biliary cirrhosis

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5
Q

Secondary biliary cirrhosis

etiologies

A

prolonged extrahepatic bile duct obstruction

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6
Q

Primary sclerosing cholangitis

association

A

ulcerative colitis

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7
Q

Primary sclerosing cholangitis

pathology

A

autoimmune fibroinflammatory destruction of intrahepatic AND extrahepatic bile ducts
fibrous plugs in place of bile ducts in portal canal

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8
Q

Complications of primary sclerosing cholangitis

A

strictures of bile ducts at different locations

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9
Q

Hemochromatosis

pathology

A

mutation of HFE gene
hepcidin not produced when iron is high
ferroportin not degraded on apical surface of intestinal epithelium
excess iron absorbed

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10
Q

Skin in hemochromatosis

A

slate gray skin

hemosiderin and malnin buildup in dermal macrophages

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11
Q

Where does Fe build up in hemochromatosis

A

1˚: periportal hemosiderin

2˚: in Kuppfer cells

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12
Q

Bronze diabetes

A

hemochromatosis DM + skin pigmentation

also cirrhosis

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13
Q

Screening for hemochromatosis

A

fasting transferrin saturation

diagnostic: liver Bx w/ quantitative Fe

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14
Q

Wilson’s disease mutation

A

ATP7B mutation
cannot get Cu into bile
so cannot excrete

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15
Q

Test results in Wilson’s

A

decreased ceruloplasmin

increased urinary Cu

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16
Q

Liver disease in A1AT deficiency

A

not in null-null: no A1AT produced, so does not build up

mutated protein –> builds up (ZZ and MM homozygotes)

17
Q

Mechanisms of drug-induced hepatotoxicity

A
direct hepatotoxicity (dose-dependent)
unpredictable/idiosycratic: unpredictable
18
Q

Budd-Chiari syndrome

A

hepatic vein thrombosis

hepatomegaly, ascites, abdominal pain

19
Q

Granulomatous hepatitis

possible etiology

20
Q

HELLP syndrome

A

hemolysis, elevated liver enzymes, low platelets

in pre-eclampsia

21
Q

BM transplants and liver

A

graft vs host

sinusoidal obstructive syndrome

22
Q

ALT and AST

information

A

hepatocyte damage

ALT > AST more specific for liver damage

23
Q

Alkaline phosphatase

information

A

cholestasis/damage to bile duct epithelium

also due to bone pathologies

24
Q

GGT

information

A

when alkaline phosphatase may be due to bone disease

25
Wilson's usually presents by this age
30 y/o | consider in all liver disease
26
PE in Wilson's
ring of copper at cornea limbus | Kayser-Fleischer ring
27
A1AT inheritance
autosomal co-dominant
28
A1AT balances
neutrophil elastase in lungs
29
``` Tests for: viral hep: autoimmune hep: Wilson's: A1AT: hemochromatosis: 1˚ biliary cirrhosis: ```
viral hep: serology, nuclear DNA/RNA autoimmune hep: ANA, anti-sm muscle Ab Wilson's: ceruloplasmin A1AT: A1AT level, phenotype hemochromatosis: Fe, TIBC, transferring sat, genetics 1˚ biliary cirrhosis: anti-mitochondrial Ab
30
Grade vs State
grade: amt of lymphocytic piecemeal and lobular necrosis staging: degree of necrosis
31
Cirrhosis vs fibrosis
cirrhosis: fibrosis w/ nodular regeneration