GIT 2 Flashcards

1
Q

Cavernous hemangioma involves ____ structures and has _______ appearance

A

deep (liver, brain)

“Mulberry like”

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2
Q

Cavernous hemangioma histology:

A

Abnormal dilated blood vessels with single epithelial layer and thin adventitia lacking elastic fibers and smooth muscles

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3
Q

Focal nodular hyperplasia is most common in _____. it is a _______ lesion caused by hepatic vascular abnormality causing ______ with ________

A

young women. non-malignant

localized hyperperfusion, secondary hyperplasia

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4
Q

Focal nodular hyperplasia features indicating arterial origin is _____________________________

A

enhancement with contrast in arterial phase

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5
Q

Crigler Najjar syndrome type 1 treatment

A

plasmapheresis and phototherapy

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6
Q

Wilson disease lab findings:

A

↓ ceruloplasmin, ↓ bound copper, ↓ Total copper

↑ Free copper ( cause of all the symptoms)

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7
Q

(ATP7B gene; chromosome 13)

A

hepatocyte copper-transporting ATPase → loads Cu to apoceruloplasmin → it loads Cu to ceruloplasmin → secreted in blood

  1. Transports Cu to bile
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8
Q

Hemochromatosis effect on gonads and joints

A

hypogonadism (atrophy of testis)

arthropathy (calcium pyrophosphate deposition; especially metacarpophalangeal joints).

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9
Q

HFE protein found on

A

basolateral surface of hepatocyte and enterocyte

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10
Q

Ferroportin found on

A

macrophages and basolateral surface of enterocyte

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11
Q

Hemochromatosis

On ____ gene, located on chromosome ___; associated with ____. Leads to ______ and _________

A

HFE , 6

HLA-A3

abnormal iron sensing and ↑intestinal absorption

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12
Q

Primary sclerosing cholangitis

Unknown cause of concentric “onion skin” bile duct fibrosis alternating strictures and dilation with “beading”

A

of intra- and extrahepatic bile ducts

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13
Q

Primary biliary cholangitis
Autoimmune reaction lymphocytic infiltrate +/– granulomas destruction of ____

Treatment:

A

lobular bile ducts.

Ursodiol (ursodeoxycholic acid)

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14
Q

Estrogen increases the biosynthesis of cholesterol by___

A

upregulation of HMG-CoA reductase

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15
Q

Ursodeoxycholic acid is only used for____

A

cholesterol stones

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16
Q

Pigment stones (black =

brown =

A

radiopaque, Ca2+ bilirubinate, hemolysis

radiolucent, infection

17
Q

Choledocholithiasis Presence of gallstone(s) in

A

common bile duct

18
Q

Rigler triad:

A

radiographic findings of pneumobilia, small bowel obstruction, gallstone (usually in iliac fossa).

used for gallstone ileus

19
Q

Charcot triad of cholangitis includes ____

Reynolds pentad is _____

A

JFR: jaundice, fever, RUQ pain.

Charcot triad plus altered mental status and shock (hypotension).

20
Q

TPN causes bile stone by

A

↓CCK release → hypomobility of bile

21
Q

Recurrent abdominal pain and jaundice in childhood (<10 y)

A

Choledochal cysts: Congenital dilatation of common bile duct

22
Q

Abdominal pain, high fever 10 - 14 days after acute pancreatitis:

A

pancreatic abscess due to infection of pancreatic pseudocyst.

23
Q

Pancreatic pseudocyst (lined by _____ , not _____

A

granulation tissue

epithelium

24
Q

Chronic pancreatitis Complications include

A

pancreatic insufficiency and pseudocysts.

25
Q

Pancreas lies below _____

A

splenic vein

26
Q

Splenic vein thrombosis treatment:

A

splenectomy

27
Q

Pancreatic adenocarcinoma

Very aggressive tumor arising from ______

A

pancreatic ducts

28
Q

Pancreatic adenocarcinoma

Associated with tumor marker _______ (also _____, less specific).

A

CA 19-9,

CEA

29
Q

——-, ———– and ———- genes are mutated in pancreatic carcinoma

A

BRCA-2, K-RAS, SMAD-4 (DPC-4)

30
Q

Normally Fatty acids exist in the serum ___

A

bound to albumin

31
Q

Effect of acute pancreatitis on sodium:

A

Hypernatremia (third spacing → hypovolemia → renal sodium retention