GIT 1 Flashcards

(33 cards)

1
Q

Pancreatic secretions

A

Isotonic fluid; low flow → high Cl−, high flow → high HCO3−.

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2
Q

Pancreatic proteases

A

trypsin, chymotrypsin, elastase, carboxypeptidases

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3
Q

Trypsinogen Converted to active enzyme by

deficiency:

A

enterokinase/ enteropeptidase,

both fat and protein malabsorption

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4
Q

Peyer patches location

A

Unencapsulated lymphoid tissue, found in lamina propria and submucosa of ileum

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5
Q

_______ catalyzes rate-limiting step of bile acid synthesis.

A

Cholesterol 7α-hydroxylase

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6
Q

Best initial test for cholestasis is

A

USG

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7
Q

Conjugated bilirubin undergoes 2 reactions in gut carried out by bacteria:

A
  1. Conjugated → Unconjugated by beta-glucuronidase

2. Unconjugated → Urobilinogen

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8
Q

Bile duct obstruction: Urine findings

A

Bilirubin in urine (dark urine)

Absent urobilinogen → Absent urobilin

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9
Q

Breast milk jaundice causes _____ hyperbilirubinemia that peaks at age of _____

A

indirect, 2 weeks

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10
Q

Breast milk jaundice mechanism:

A

Beta-glucuronidase in breast milk decojugates bilirubin → ↑absorption → ↑enterohepatic circulation of bilirubin

Urine and stool appearance unchanged

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11
Q

Dubin johnson syndrome: defect in _______

Why NO PRURITIS?

A

Multidrug resistance proteins

pruritis is caused by BILE SALTS. in obstructed diseases bile salt is not excreted and accumulates in skin causing PRURITIS

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12
Q

Biliary atresia: Fibro-obliterative destruction of _________

presentation:

A

extrahepatic bile ducts

newborn with persistent jaundice after 2 weeks of life, darkening urine, acholic stools, hepatomegaly.

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13
Q

Physiologic neonatal jaundice

A

At birth, immature UDP-glucuronosyltransferase , short HL of RBCs, ↑enterohepatic circulation of bilirubin (due to low bacteria in GIT) ► unconjugated hyperbilirubinemia

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14
Q

Physiologic neonatal jaundice Occurs ____ first 24 hours of life and usually resolves without treatment in ____

A

after

1–2 weeks

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15
Q

Crigler Najjar syndrome Type II is less severe and responds to ____ which _____

A

phenobarbital,

↑ liver enzyme synthesis.

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16
Q

Effect of cirrhosis on heart:

A

high output heart failure due to chronic splanchnic vasodilation and development of shunts

17
Q

Sinusoidal HTN:

A

loss of protein rich fluid in space of Disse → ↑formation of hepatic lymph → Ascites

18
Q

Parthenogenesis of autoimmune hepatitis

A

molecular mimicry

19
Q

AST > ALT in nonalcoholic liver disease suggests _____

A

progression to advanced fibrosis or cirrhosis

20
Q

Fulminant hepatitis:

A

Hepatic encapth within 6 weeks of hepatiic insult

21
Q

Underlying mechanism of fulminant hepatitis is ___

A

hypersensitivity reaction to drug → immune mediated attack against hepatocytes.

22
Q

Autopsy findings of fulminant hepatitis:

A

atrophy and shrunken

23
Q

Alcoholic hepatitis histology

A
Swollen and necrotic hepatocytes with neutrophilic infiltration. 
Mallory bodies  (intracytoplasmic eosinophilic inclusions of damaged keratin filaments).
24
Q

Fibrous tissue (thickened collagenous bands) is stained with

A

stained blue with Masson trichrome stain

25
Hepatic encephalopathy → ↓NH3 removal causes
(due to renal failure, diuretics, bypassed hepatic blood flow post-TIPS).
26
the liver is the site of production of all major coagulation factors, except _______
factor VIII.
27
symptoms of volvulus:
bilious vomiting, abdominal distention, and bloody stools.
28
In children, volvulus almost always occurs in the _____
small intestine
29
in liver Acetaminophen is known to cause _____
centrilobular necrosis
30
drugs associated with granuloma formation include _____
SHAQ | sulfonamides, hydralazine, allopurinol, quinidine,, and methyldopa
31
______ can chelate and ↓effectiveness of other drugs (eg, tetracycline)
Calcium carbonate (antacid)
32
Hypolglycemia in hepatocellular carcinoma due to:
1. ↑ metabolic rate of tumor | 2. produces insulin like growth factor-II
33
Most common benign liver tumor_____
cavernous hemangioma