Liver Pathology Flashcards

(31 cards)

1
Q

Zone for ischemic injury?

Bile duct gets blood from?

ITO cell hyperplasia from?

A

Zone 3 near central vein (blood goes from zone 1 to zone 3)

Hepatic artery

Hypervitaminosis A; leads to fibrosis and cirrhosis

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2
Q

Acetaminophen toxicy causes?

H and E?

Tx?

A

Fulmenant liver failure

Necrosis without inflammation in ZONE 3 (most C450 enzyme highest here); NAPQI is the toxic molecule

NAC

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3
Q

Acute inflammaiton happens where in liver?

Chronic hepatitis happens where?

Canallicular cholestatis only; common clinically in what scenario?

Ductual cholestatis (ducts with inspisated bile) think?

A

Lobule (lobular disarray)

Portal tracks/periportal

Estrogen and steroids in young men

Sepsis

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4
Q

EBV hepatitis you see?

Bridging fibrosis think?

Which Hepatitis is DNA?

What Hep casues HCC?

A

Lymphocytes in the Sinusoids

Autoimmune hepatitis

Hep B (other RNA)

B,C, D

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5
Q

Chronic hepatisis H and E?

Hep C genotype associated with steatosis?

Other causes?

A

“Blue portal tracts” and some steatosis

3

Hep B, C, D; Chronic autoimmune, emds, Wilson, Alpha-1 antitrypsin, Lymphoma

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6
Q

Ground glass hepatocyts, think?

Most common Autoimmune hepatitis?

Tx?

H and E?

A

Hepatitis B from proliferating endoplasic responding to HbsAg

Type 1 adults (P-ANCA); type 2 in kids (anti-LKM1)

Tx: Steroids

Portal inflammation, Zone 3 with inflammation (vs tylenol which has no inflammation)

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7
Q

A1-antitrypsin, gene?

See what clinical issues?

H and E?

PiM means?

A

Chr14; SERPINA1 gene; folding abnormality and doesn’t go into blood

Emphysema (can’t inhibit elsastase) and chronic liver disease

H and E: Periportal PAS-D globules adn hepatitic changes

PiM normal

PiS and PiZ common deficency alleals (Z lowest production)

PiZZ most severe

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8
Q

Hereditary Hemochromatosis gene, presentation?

H and E?

Special stain?

A

Auto recessive; HFE gene (C282Y–highest Fe Overload and H63D), Diabetes, skin pigmentation, cirrhosis

Hepatocytes around zone 1; vs blood transfusions show hemosidering in Kupfer cells

Prussian blue

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9
Q

Gene in Wilsons?

Copper is where in eyes?

Liver H and E?

Lab test?

Know EM has seperations and increased matrix and crystaline inclusions

A

ATP7B; copper transporter in Golgi

Descement membrame

Steatosis, hepatitis, glycongenated nuclei, Mallory hyaline, Copper by Rhodanine

Common low ceruloplasmin and increased urine copper

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10
Q

Bland cholestasis caused by what drugs?

Is periportal copper always Wilson’s?

A

Estrogen and anabolic steroids (intrahepatic only)

NO! Can be from biliary damage

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11
Q

What is primamry billiary cholangitis?

Antibody?

Elevated Ig?

H and E?

A

Autoimmune; loss of intrahepatic bile ducts; Mid age females; Puritis

Antimitochondrial antibody; some AMA negative

IgM vs IgG in autoimmune

Chronic cholestatis, florid bile duct lesion–lymphocytes, non-caseating granulomas, increased copper

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12
Q

Primary Schlerosis Choleangitis disease, population, Key association?

H and E?

ERCP picture?

A

Fibroinflammatory disease; intra and extrahepatic biliary tree; Males, UC 65%; risk cholangiosarcoma

Fibrous obliteration of bile ducts: Periductal fibrosis (onion skin) and Ductopenia (with proliferation and damage)

Beads on a string

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13
Q

Macrovesicular steatosis causes?

A

Obesity, diabetes, metabolic syndrome

Malnutrition, TPN

Alcohol

WIlson’s

Hep C

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14
Q

Micro vesicular steatosis causes?

A

Nuclei indented with fat vacuoles

Pregnancy (AFLD)

Reye’s

Drugs

Valproic acid

Mushrooms

Tetracycline

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15
Q

Where does steatohepatis start?

Stain Mallory-Denk bodies?

Drugs that make Mallory hyaline?

A

Zone 3:

Mallory-Denk bodies: p62+, ubiquitin; intermediate filaments metabolized by cytokeratin from injury

Amiodarone (granular hepatocytes with lysozome inclusions on EM); Methotrexate, Tamoxifen

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16
Q

Fibrin ring granuloma think?

Hydadid cyst, contact with?

Worry if contents spills?

Hydatid sand is?

A

Q-Fever, Coxiella burnetiil; fat globule, fibrin and granuloma

Sheep and dogs; Echinoccous Granulosis, Lamanated membrane GMS+

Anaplylaxis

Capsules, free scolices and loose hooklets

17
Q

Non-zonal (geographic) necrosis think about?

A

Herpes (hemmorhage common) and Adenovirus (smudgy nuclei) are common

18
Q

Zone prone to ischemia?

Gross?

A

Zone 3 coagulative necrosis without inflammation; some intralobulal bile duct damage possible

Nutmeg liver

19
Q

Budd-Chiari is?

H and E?

Common clinical?

A

Suprahepatic vein outflow issues; Polycythemia vera, infections, malignancy

Sinusoidal dilation, congestion (RBCs), hemorrhage, hepatocyte atrophy

2-3 weeks post stem cell transplant from chemo

20
Q

What is hepatoportal sclerosis?

DDx?

A

Central vein abnormally close to portal areas; Portal fibrosis with portal vein narrowing or obliteraiton

Portal vein thrombosis

21
Q

What is nodular regenerative hyperplasia?

Disease associations?

Does it cause portal hypertension?

A

Nodules in parenchyma; Trichrome negative; reticulin highlights nodules

Rheumatologic, PV, lymphoma, azathioprine

Yes! Reticulin shows compressed portal between nodules, variable hepatocyte sizes

22
Q

What is a hepatic adenoma?

Associated with?

Reticulin and CD34 staining?

Tx?

A

Solitary, well circumscribed, non cirrhotic, Benign hepatocytes (1-2 layers thick); clear cell glycogen chagnes; NO PROTAL TRIADS just naked arteries

Oral contraceptives

Intact reticulin, CD34 increased

Tx: Surgery, malignant rare

23
Q

What type of hepetic adenoma has HCC risk?

IHC?

A

B-Catenin; 10% of adenomas, cytologic atypia present

IHC: Beta-catenin and diffuse glutamine synthetase (Staining pattern similar to HCC; not useful)

24
Q

Two liver lesions with scar?

FNH, population?

H and E?

IHC?

A

Fibrolamellar carcinoma and focal nodular hyperplasia

Women 3rd-4th decade and kids txed for malignancy; Not associated with OCP

Non-cirrhotic, Hepatocytes divided into nodules but hick walled arteries (at edges) in fibrous septate, ductular reaction at junction

Map like glutamine synthetase (spared around scar and septae)

25
HCC associated with in China, organism? HCC H and E?
Alpha toxin B1 from aspergillus ; Also **Cirrhosis common** Mimics liver; trabelcular growth or pseudoglandular gwoth (single layer of tumor cells and dilated canaliculi)**, can have bile mallory/hyaline/A1-AT bodies, or thick trabeculae lacking protal areas**
26
HCC IHC?
CD34+ (can be in adenomas) **Glypican III + (- in benign; can be - in 50% of HCC)** Reticulin disrupted HepPar1+ (also gastric and some adeno) Arginase +, pCEA + (canallicular)
27
Fibrolamellar carcinoma? Gross finding? H and E? IHC? Gene?
10-35 yr oldCentral Scar: **No cirrhosis** Malignant with large eosinophilic granular cytoplasm, with vesicular nuclei and nucleoli think; **Parallel fibrosis** **CK7+ (most HCC -), CD68+**, AFP -, **DNAJB1-PRKACA**
28
Cholangiocarcinoma? H and E? IHC? Risk factors?
Older patient; **No histor of cirrhosos in most**; Desmoplastic fibrous strome, **LVI common, glands** CK7+, HepPar1-, Arginase-, CK20-, CDX2-, CK19+, MOC31+ Fluke infection (**Clonorchis sinensis or Opisthorchis)**, PSC, hepatolithiasis, bile duct abnormalities
29
Bost common benign tumor of liver? H and E? EHE H and E? Gene?
Hemangioma, 2nd is FNH Rarely biopsied; Cavernous vasculiture with no atypia EHE: Abundant myxoid matrix. Dendritic/epithelioid tumors, **intracytoplasmic RBCs** **t(1;3) WWTR1-CAMTA1** CD34+, ERG+. CD31+, FLI1+, FVIII +, D2-40+
30
Black liver with elevated direct bilirubinemia? Pattern of inheritance Gene? Other cause of hyperbilirubinemia?
Dubin Johnson; **Benign; Urine shows normal porphorins** Auto Reccesive **cMOAT/MRP2** gene with impaired biliary transport of conjugated bilirubin (direct) **Rotor syndrome (non black liver)**
31