March 16 - GI Flashcards

(50 cards)

1
Q

Osmotic laxatives

A

Polyethylene glycol, magnesium citrate

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2
Q

Pigment stones: two causes

A
  1. Infection of biliary tract with bacteria or helminths. Causes release of beta glucuronidase which increases unconjungated bilirubin by deconjugating bilirubin

2, Crhonic hemolytic anemia

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3
Q

Opioids and gallbladder

A

Opioids can cause contraction of sphincter of Oddi. This increases bile duct pressures causing biliary colic

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4
Q

Graft-vs-host disease: liver

A

Lymphatic infiltration and destruction of small intrahepatic bile ducts, similar to what is seen in PBC

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5
Q

Riboflavin deficiency

A

Riboflavin used to make FAD which is involved in TCA cycle and electron transport chain. In TCA cycle, needed for succinate dehydrogenase.
Def causes stomatitis, chelitits, glossitis, seborrheic dermatitis, anemia

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6
Q

TCA cycle steps

A
  1. pyruvate to oxaloacetate
  2. oxaloacetate to citrate
  3. citrate to isocitrate
  4. isocitrate to alpha ketoglutarate + NAD to NADH
  5. alpha ketoglutarate to succinyl coA + NAD to NADH
  6. succinyl coA to succinate + GDP to GTP
  7. succinate to fumarate + FAD to FADH2
  8. fumarate to malate
  9. malate to oxaloacetate + NAD to NADH
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7
Q

C diff colitis: toxins

A

enterotoxin A: causes watery diarrhea
cytotoxin B: causes colonic epithelial cell necoris and fibrin deposition

Both disrupt actin cytoskeleton, sirupting itght junctions

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8
Q

Lipid digestion: location

A

Digestion occurs in duodenum

Abosrption occurs in jejunum

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9
Q

Pus formation

A

Macrophages at site release IL-8 which calls in neutrophils

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10
Q

C3a vs C5a

A

C3a: chemotactic for basophils and eosinophils
C5a: chemotactic for neutrophils

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11
Q

Pancreatic pseudocysts

A

Occurs as complication of acute pancreatitis. Pancreatic enzymes leak out leading to inflammatory reaction. Granulation tissue forms and encapsulates fulid. Not a true cyst because it is lined by granulation tissue rather than epithelium. Over 4-6 weeks, granulation tissue develops into fibrosis.

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12
Q

Causes of intestinal atresia

A

Duodenal: failure of recanalization
Jejunal/ileal: vascular injury; decreased perfusion results in ischemia which results in narrowing or obliteration of a segment of bowel
Colonic: cause unknown

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13
Q

Arsenic poisioning: presentation, causes, treatment

A

Causes: insecticide ingestion, contaminated well water

Presentation

  • acute: garlic odor, vomiting, profuse watery diarrhea, QT prolongation
  • chronic: hypo or hyperpigmentation, hyperkeartosis, stocking glove neuropathy

Treatmnet: dimercaprol (chelator that increases urinary excretion)

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14
Q

Deferoxamine

A

Chelator for iron OD

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15
Q

CaNa2 EDTA

A

chelator for lead toxicity

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16
Q

Hydroxycobalaminin

A

antidote for cyanide poisoning

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17
Q

Methylene blue

A

treatment for methemoglobinemia

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18
Q

Hamartonatous polyps

A

Generally benign polys. Disorganized mucosal glands, smooth muscle, connective tissue. Sporadic or associated with Peutz Jehghers or juvenile polyposis.

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19
Q

Budd chiari syndrome: pathology and pathophysiology

A

Pathology: Dilation of sinusoids, perivenular hemoorhage
Cause: acute venous outflow obstruction in liver

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20
Q

Anal fissure: presentation and location

A

Presentation: sharp pain + bright red bleeding with defecation

Location: Posterior midline anus distal to dentate line

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21
Q

Gastric varices

A

Two causes

1) portal HTN as complication of cirrhosis
2) splenic vein thrombosis as complication of chronic pancreatitis or pancreatic cancer. Short gastrics drain the fundus to thrombosis of the splenic vein increases pressure in the short gastrics and causes gastric varices isolated to the fundus

22
Q

Azygos veins and left gastric vein

A

Azygos: drains esophageal veins to SVC

L gastric: drains upper stomach and lower esophagus to portal vein

23
Q

Crohns and gallbladder

A

Terminal ileum inflamed in Crohns. Can’t reabsorb bile acids, resulting in increased cholesterol to bile ratio and gallstone formation

24
Q

PAS stain

A

Stains glycoproteins bright pink. Good for looking at fungal cell walls, mucus secretions, BMs. In GI good for looking for T whippelii in sm bowel (gram po actinomycete)

25
Portal vein thrombosis
Portal HTN with liver unacffected as it si a perisinusoidal process
26
CA19-9
Pancreatic cancer marker
27
CA 125
Ovarian cancer marker
28
Carcinoembryonic antigen
GI cancer marker
29
Crohns vs UC inflammation
Crohns: Th1 process resulting in granulomas UC: Th2 process resulting in mucosal damage
30
Indirect inguinal hernia: population,anatomy, cause
Population: male infants Anatomy: superior to inguinal ligament. Lateral to inferior epigastrics. Protrudes through deep and superficial rings and is coveretd by all three fascial laters Cause: Patent processus vaginalis
31
Direct inguinal hernia: popualtion, anatomy, cause
Population: old men Anatomy: superior to inguinal ligament. Medial to inferior epigastrics. Protrudes through Hesselbach's triangle. Superficial ring only. Covered by external spermatic fascia only Cause: weak transfersalis fascia
32
Femoral hernia: population, anatomy, cause
Population: women Anatomy: protrudes through femoral ring, inferior to inguinal ligament Cause: weak proximal femoral canal
33
Conjugated vs unconjugated bilirubin
Conjugated is water soluble and excess can be excreted in urine
34
Cavernous hemangioma
Most common benign tumor of liver. Most common in adults 30-50. Often asymtpomatic. No biopsy due to risk of bleeding.
35
Liver tumor associated with oral contraceptives
hepatic adenoma
36
Zenker diverticulum: pathophysiology and presentation
Pathophys: Abnormal action of cricopharyngeal muscles during swallowing (either spasm or failure to relax) results in increased pressure in the pharynx resulting in herniation of pharyngeal mucosa to form a false diverticulum Presentation: dysphasia, coughing/choking sensation, halitosis, recurrent aspiration pneumonia
37
Biliary sludge
Forms due to gallbladder hypomotility. Precursro to gallstones
38
Cystinuria
Autosomal recessive. Increased urine cysteine. Early cysteine kidney stones.
39
Locations of heart chambers
LA: most posterior, can compress underlying esophagus RV: lateral right heart RA: anterior and superior LV: left lateral heart
40
Diverticulitis: pathophys/pathology
Pulsion: increased pressure from straining leads to herniation of the mucosa and submucosa through weak areas of the muscularis Most common in sigmoid colon False diverciulum as does not include muscularis layer
41
Bethanechol
Muscarinic agonist
42
Cimetidine
H2 blocker
43
Reye syndrome
1. Hepatic dysfunction: vomiting, hepatomegaly, and increased LFTs. On path, microvescular steatosis (small fat vacuoles in hepatocyte cytoplasm) 2. Encephalopathy: due to increased ammonia
44
Two types of stomach cancer
1. Diffuse type: signet ring cells (nucleus pushed to side), non-gland forming, diffuse involvement due to loss of e-cadherin 2. Intestinal type: resembles colon cancer with well formed glands, grows as a well formed mass
45
Acute viral hepatitis: pathology
ballooning degeneration councilman bodies: eosinophilic/acidophilic apoptotic hepatocytes mononuclear infiltrate
46
Non-atrophic vs atrophic chronic gastritis
Non-atrophic: In antrum, usually due to H pylori, and leads to duodenal ulcers Atrophic: inflammation in body and fundus leading to loss of acid producing cells, risk for cancer
47
Pathogenesis of cholesterol gallstones
Increased cholesterol Decreased bile acids Decreased phosphatidylcholine
48
Kaposi's sarcoma in GI
Can cause diarrhea. Diagnosed by scope which shows red/violet maculopapular lesions to raised hemorrhagic nodules. Biopsy shows spindle cells and BV proliferation
49
NEcrotizing enterocolitis: presentation, pathogenesis, and diagnossis
Presentation: distension and bloody stools in a preemie. Pathogenesis: feeding introduces bacteria to bowel which proliferate excessively, invade the wall, and cause inflammation and ischemic necrosis Diagnosis: thin curvilinear areas of lucency that parallel gut lumen on x-ray
50
Pathogenesis of hepatic steatosis in alcoholics
Incareds NADH produced by EtOH metab | Results in decreased FFA oxidation and accumulation of TGs