Exocrine Pancreas, GB and Liver Flashcards

1
Q

What causes Acute pancreatitis

A
  1. Alcohol
  2. Gallstones
  3. Hypercalcemia
  4. Hyperlipidemia
  5. Drugs
  6. Scorpion sting
  7. Mumps
  8. Rupture of posterior duodenal ulcer
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2
Q

Pancreatic pseudocysts

A

Fibrous tissue surrounded liquefactive necrosis and pancreatic enzymes seen as late complication of Acute pancreatitis

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3
Q

What cuases Chronic Pancreatitis

A

Aduts: alcohol

Children: CF

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4
Q

Pancareatic carcinoma tumor marker is

A

CA 19-9

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5
Q

Pancreatic carcinoma is an

A

adenocarcinoma arising from the pancreatic ducts

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6
Q

Pancreatic carcinoma clinical

A
  1. Obstructive jaundice with pale stools and papable GB: because tumor normall in Head of pancreas causing obstruction
  2. Migratory thrombophlebitis (Trousseau sign)
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7
Q

Cholelithiasis is

A

Gallstones

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8
Q

Cholelithiasis arrise due to

A
  1. Saturation of Cholestrol or bilirubin
  2. Decrease phospholipds (Lecithin) or bile acids
  3. Stasis
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9
Q

Cholesterol stones are

A

Yellow

Radiolucent

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10
Q

Risk factors for cholesterol Gallstones

A
  1. Age
  2. Estrogen
  3. Clofibrate (increase cholesterol production)
  4. Crohn
  5. Cirrhosis
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11
Q

Bilirubin stones are

A

Pigmented Radiopaque

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12
Q

What two bugs increase Bilirubin Gallstones

A

Ascaris lumbricoides

Clonorchis sinensis

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13
Q

Acute cholecystits pain originates and radiates to where

A

Right upper quadrant pain that radiates to right scapula

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14
Q

Rokitansky-Aschoff sinus

A

Herniation of GB mucosa into muscular wall seein in chronic cholecystits

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15
Q

Ascending cholangitis is due to infection with

A

Ascending enteric gram-negative bacteria

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16
Q

What conjugates bilirubin in hepatocytes

A

Uridine glucuronyl transferase

17
Q

Gilbert syndrome genetics

A

AR mutation causing mildly low UGT activity

18
Q

Gilbert syndrome lab findings

A

Increase UCB

19
Q

Gilbert syndrome clinical

A

Jaundice during stress

20
Q

Crigler-Najjar defect

A

Absence of UGT

21
Q

Crigler-Najjar clinical

A

Kernicterus

Fatal

22
Q

Dubin-Johnson genetics

A

AR deficiency of bilirubin canalicular transport protein

23
Q

Dubin-Johnson lab findings

A

Increased CB

24
Q

Lab findings in Obstructive jaundice

A
  1. Increase CB
  2. Decrease urine Urobilinogen
  3. Increase Alkaline phosphate
25
Q

Fibrosis in Cirrhosis is mediated by

A

TGF-β from Stellate cells

26
Q

Mallory bodies are

A

Damaged cytokertain filaments seen in alcohol-related hepatitis

27
Q

Primary hemochromatosis is due to an AR mutation in

A

HFE gene

28
Q

Triad of Hemochromatosis

A

Cirrhosis

Secondary Diabetes mellitus

Bronze skin

29
Q

Hemochromatosis lab findings

A
  1. Increase ferritin
  2. Decreased TIBC
  3. Increased Serum Iron
  4. Increased % saturation
30
Q

Wilson disease genetics

A

AR defect in ATP7B that is an ATP-mediated hepatocyte Cu transport

31
Q

Treat wilson disease with

A

D-pencillamine (chelates copper)

32
Q

Primary Sclerosing Cholangitis is

A

Inflammation and fibrosis of intrahepatic and extrahepatic bile ducts

33
Q

Primary Sclerosing Cholangitis is associated with

A

UC

p-ANCA

34
Q

Reye syndrome is

A

Liver failure and encephalopathy in children with viral illness taking asprin

35
Q

Aflatoxin is a risk factor for

A

Hepatocellular carcinoma

36
Q

Hepatocellular Ca serum tumor marker is

A

Alpha-fetoprotein