NEET PG Pathology MCQs 171 – Liver, Gall bladder, Pancreas Disorders – 4

1.HBeAg in a patient of hepatitis signifies

  1. Chronic nonactive hepatitis
  2. The patient is infectious & active viral replication
  3. Chronic persistent hepatitis
  4. Acute hepatitis with low infectivity

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2. Most common route hepatitis E transmission is

  1. Sexual
  2. Faeco-oral
  3. Horizontal
  4. Vertical

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3. Gene responsible for the mutation of HBV is

  1. X gene
  2. S gene
  3. P gene
  4. C gene

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4. A nurse got a needle prick injury, Which of the following suggests active phase of hepatitis

  1. IgM Ab HBc
  2. IgG Ab of Hbc
  3. IgG of HBs
  4. Anti Hbe Ab

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5. A most common subtype of hepatitis B in north India Is

  1. Adr
  2. Adw
  3. Ayw
  4. Ayr

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6. Hepatitis virus that causes chronic liver disease is

  1. Hepatitis A
  2. Hepatitis B
  3. Hepatitis C
  4. Hepatitis D

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7. Ground glass hepatocyte is seen in which hepatitis

  1. Hepatitis A
  2. Hepatitis B
  3. Hepatitis D
  4. Hepatitis E

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8. Councilman bodies are seen in

  1. Alcoholic cirrhosis
  2. Wilson’s disease
  3. Acute viral hepatitis
  4. Autoimmune hepatitis

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9. Microvesicular fatty change in hepatocytes is seen due to infection with

  1. Hepatitis A
  2. Hepatitis B
  3. Hepatitis C
  4. Hepatitis D

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10. Histopathology of chronic hepatitis shows

  1. Ballooning of hepatocytes
  2. Councilman bodies
  3. Bridging fibrosis
  4. All of the above

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11. Which of the following is the single most important indicator of the likelihood of progression of hepatitis to liver cirrhosis

  1. Etiology
  2. Associated serological findings
  3. Presence of bridging necrosis
  4. Presence of Mallory hyaline bodies

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12. Macronodular cirrhosis occurs in

  1. Postnecrotic
  2. Cryptogenic
  3. Biliary cirrhosis
  4. Wilson’s disease

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13. Lipoprotein-X is elevated in

  1. Hypercholesterolemia
  2. Primary biliary cirrhosis
  3. Indian childhood cirrhosis
  4. Alcoholic cirrhosis

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14. Which one of the following is not a feature of liver histology in non-cirrhotic fibrosis

  1. Fibrosis in and around the portal tracts
  2. Thrombosis of the medium and small portal vein branches
  3. Non-specific inflammatory cell infiltrates in the portal tracts
  4. Bridging fibrosis

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15. Micronodular cirrhosis is seen in all except:

  1. Alcoholic cirrhosis
  2. Wilson’s disease
  3. Budd Chiari syndrome
  4. Indian childhood cirrhosis

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16. Macronodular cirrhosis refers to nodule diameter greater than

  1. 1 mm
  2. 2 mm
  3. 3 mm
  4. 4 mm

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17. In cirrhosis liver, all are seen except

  1. Loss of normal architecture
  2. Degeneration of hepatocytes
  3. Fatty infiltration
  4. Loss of intercellular connective tissue matrix

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18. Mr. Satish a 58-year-old man with a known case of hepatitis C and cirrhosis complains of worsening confusion over the past 5 days. He has had ascites that has been refractory to high- dose oral diuretic use.He also reports that over the past 48 hours he has had a declining urinary output. Lab results reveal a WBC of 4600, Bun of 34mg/dl and a creatinine of 3.1 mg/dl A urinary sodium is less than 10mEg/L. Most appropriate treatment for elevated BUN and creatinine

  1. Large volume paracentesis
  2. Hemodialysis
  3. Mesocaval shunt
  4. Liver transplantation

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19. All are seen in hemochromatosis except:

  1. Hypogonadism
  2. Arthropathy
  3. Bronze diabetes
  4. Desferrioxamine is the treatment of choice

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20. Kayser-Fleischer ring is seen in

  1. Wilson’s disease
  2. A-1 antitrypsin deficiency
  3. Hemochromatosis
  4. Primary biliary cirrhosis

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21. All are true Wilson’s disease except

  1. Liver Cu
  2. Urine Cu
  3. Ceruloplasmin
  4. Serum Cu

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22. Liver in hemochromatosis is stained by which of the following stain

  1. Perls iron stain
  2. Alcian blue
  3. Congo red
  4. Masson trichome

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23. PAS-positive diastase-resistant globules hepatocytes are seen in

  1. Hemochromatosis
  2. Wilson’s disease
  3. Alpha 1 antitrypsin deficiency
  4. Acute necrotic hepatitis

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24. Hemochromatosis is a defect in the metabolism of

  1. Iron
  2. COPPER
  3. Magnesium C
  4. calcium

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25. gene for Wilson’s disease is located on chromosome

  1. 7
  2. 10
  3. 13
  4. 17

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