Gi uworld 1 Flashcards

1
Q

Hematochezia, Tc-pertechnetate scintigraphy demonstrates focal radiotracer accumulation in the right LQ. failed embryologic process?

A

failed obliteration of the vitelline duct

  • Meckel diverticulum: incomplete closure of the vitelline duct results in an ileal outpouching with a fibrous connection to the umbilicus
    Meckel’s diverticulum contains ectopic gastric mucosa. secretion of HCl causes small bowel ulceration and bleeding (painless lower Gi bleeding) and anemia.
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2
Q

failure of craniocaudal neural crest cell migration results in aganglionic sigmoid colon/rectum that is narrow and inactive

A

Hirschsprung disease

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3
Q

abnormal midgut rotation around the SMA

A

intestinal malrotation.

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4
Q

Zenker diverticulum - cricopharyngeal motor dysfunction

A

abnormal spasms or diminished relaxation of the cricopharyngeal muscles during swallowing (underlying mechanism).
- results in oropharyngeal dysphagia with a feeling of food obstruction at the level of the neck and coughing/choking.
- increases oropharyngeal intraluminal pressure results in herniation of the pharyngeal mucosa through the zone of muscle weakness (false diverticulum) in the posterior hypopharynx (Killian triangle)
- patients develop food retention with halitosis/regurgitation.
pulmonary aspiration of diverticular contents may lead to recurrent pneumonia.

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5
Q

degenerative changes in the myenteric plexus with impaired LES relaxation. barium swallow shows esophageal dilation with esophagogastric junction narrowing (Birds beak)

A

Achalasia

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6
Q

Rifaximin MOA in hepatic encephalopathy

A

decreased intraluminal ammonia production.

  • Rifaximin is a nonabsorbable antibiotic that alters GI flora to decrease intestinal production and absorption of ammonia. (usually given with lactulose), which is catabolized by intestinal bacterial flora to short-chain FAs, lowering colonic pH and increasing the conversion of ammonia to ammonium.
  • it is also used for traveler’s diarrhea, as it inhibits bacterial RNA synthesis through bindings with DNA-dependent RNA polymerase.
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7
Q

lactulose MOA in hepatic encephalopathy

A

increased conversion of ammonia to ammonium ions

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8
Q

hepatic encephalopathy

A

due to cirrhosis (liver’s inability to convert ammonia to urea). crosses BBB and causes altered mental status (impaired neurotransmitter release, astrocyte dysfunction, neuroinflammation, and/or edema). Asterixis (flapping tremor) is also common.

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9
Q

food protein-induced allergic proctocolitis

A

eosinophilic infiltration of the distal colon

benign condition of early infancy (<6 months).
- infants have a non-IgE-mediated reaction to proteins found in breast milk or formula (common trigger is cows milk)
painless, blood-streaked stools (loose stools with mucus) develop weeks to months after initial exposure to the food allergen

findings:

  • inflammation (erythema, edema) confined to the distal colon and rectum
  • histopathology findings include infiltration of eosinophils within the lamina propria and muscularis mucosa.
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10
Q

hemorrhagic necrosis of the bowel wall

A

Necrotizing enterocolitis. results in Gut ischemia and death if untreated.
- rectal bleeding, abdominal distension, poor feeding, hemodynamic instability

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11
Q

neutrophilic crypt abscesses

A

ulcerative colitis

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12
Q

Cystic fibrosis

A

pancreas: distension and obstruction of pancreatic ducts (pancreatic insufficiency). obstruction and distension is due to viscous mucus and inflammation.

  • recurrent sinopulmonary infections and congenital absence of vas deferens.
  • pneumonia due to a non-lactose-fermenting, gram-negative rod (Pseudomonas, Burkholderia)
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13
Q

lymphocytic infiltration of the pancreatic islet cells

A

type I DM

- destruction of insulin-producing pancreatic cells

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14
Q

nodular lymphoid hyperplasia of the intestine

A

seen in common variable immunodeficiency syndrome (low immunoglobulin and B lymphocyte levels that predispose to recurrent sinopulmonary and GI infections)

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15
Q

CMV esophagitis

A

linear, shallow ulcerations in the lower esophagus
- occurs in immunocompromised patients (HIV, transplant, immunosuppressive drugs).
CMV can be transmitted to transplant recipients from the donor organ, or infection from chronic immunosuppression.

presentation:
- odynophagia (pain with swallowing)
- dysphagia (difficulty swallowing)
- fever (or burning chest pain)

endoscopy shoes linear and shallow ulcerations in the lower esophagus

tissue biopsy shows enlarged cells with basophilic or eosinophilic intranuclear inclusion bodies

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16
Q

metaplastic columnar epithelium seen in:

A

Barrett esophagus which is due to prolonged GERD. histologically typically shows tongue-like projections of columnar epithelium with goblet cells (intestinal metaplasia) extending from the distal esophagus to the GE junction.

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17
Q

cryptococcus neoformans

A

Yeast with a polysaccharide capsule.

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18
Q

Crohns disease patient with kidney stones. cause?

A

reduced intestinal calcium oxalate formation.

  • terminal ileum involvement is usually common. when the terminal ileum is inflamed, bile acids are lost in the feces leading to impaired fat absorption
  • In crohns disease, calcium forms soap complexes with the excess fat in the intestinal lumen and is unavailable for complexing with oxalate. –> free oxalate absorption is increased and filtered into the urine, promoting the formation of oxalate kidney stones (enteric oxaluria)
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19
Q

Hepatic abscess

A

possible route: staph aureus by hematogenous route

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20
Q

presence of fluid filled cavity in the liver, with fevers, RUQ pain –> hepatic abcess.
causes

A

developing countries: parasitic infection (Entamoeba histolytica, echinococcus)

In the US: bacterial infections

pyogenic bacteria can gain access to the liver through the following routes:

  • biliary tract infection (ascending cholangitis)
  • portal vein pyemia (bowel or peritoneal sources)
  • hepatic artery (systemic hematogenous seeding) - Staph aureus infection
  • direct invasion from adjacent sources (peritonitis, cholecystitis)
  • penetrating trauma or injury
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21
Q

ascending cholangitis causes

A

enteric gram-negative bacilli (E.coli, Klebsiella) and enterococci.

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22
Q

Lymphatic drainage of the rectum proximal to the anal dentate line occurs via the inferior mesenteric and internal iliac lymph nodes.
areas distal to the dentate line drain primarily into the inguinal nodes

A
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23
Q

stronglyloid sterocoralis IgG is positive. detection of active infection?

A

rhabditiform larvae in the stool

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24
Q

carcinoid syndrome

A

wheezing, diarrhea, facial flushing in association with ileal tumor with hepatic metastasis.

  • carcinoid tumors (ileal tumors) secrete a number of active substances including serotonin
  • common manifestations of carcinoid syndrome include flushing, asthma-like symptoms (wheezing, dyspnea), diarrhea, and syncope (due to low BP)
  • long-standing Carcinoid syndrome can cause right-sided valvular heart disease

definitive therapy: surgical excision.
medical therapy with octreotide can be used to control symptoms.

octreotide is a synthetic analog of somatostatin that can be used to control symptoms. It acts on somatostatin receptors and inhibits the secretion of many hormones.

  • octreotide is also used to inhibit secretory diarrhea in VIPomas (pancreatic endocrine tumors)
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25
Q

structures directly occluded as a result of occlusion of hepatoduodenal ligament

A

hepatic artery, portal vein, common bile duct (portal triad)

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26
Q

3-day-old newborn with bilious emesis, blind-ending proximal jejunum, a length of absent bowel and mesentery, and terminal ileum spiraled around an ileocolic vessel. diagnosis?

A

intestinal atresia below duodenum

Cause: Vascular occlusion

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27
Q

enteropeptidase in the duodenal brush border activates what substance?

A

trypsin

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28
Q

enzyme causing brown pigment stones?

A

beta-glucuronidase

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29
Q

term for microscopically and functionally normal cells/tissues found in an abnormal location due to embryonic maldevelopment

A

ectopy

30
Q

lynch syndrome cause

A

nucleotide mismatch escape repair

31
Q

Dorsal pancreatic dud

A

pancreatic bud forms the pancreatic tail. body, most of the head and the small accessory pancreatic duct

32
Q

ventral pancreatic bud

A

forms the uncinate process, inferior/posterior portion of the head and the major pancreatic duct

33
Q

enzyme sequence for base excision repair

A

glycosylase, endonuclease, lysase, polymerase, ligase

34
Q

excessive alcohol use, epigastric pain, steatorrhea

A

chronic pancreatitis

35
Q

persistent diarrhea, tea colored stools, odorless watery stools. symptoms persist despite lactose free diet and fasting trial. lack of gastric acid secretion

A

VIPoma (pancreatic islet cell tumor)

36
Q

Vasoactive intestinal peptide

A

hormone for causing secretory diarrhea

37
Q

treatment of VIPoma

A

somatostatin (Octreotide)

38
Q

abdominal pain, distention, nausea, vomiting, high-pitched bowel sounds, tenderness to palpation, dilated loops of bowel with air-fluid levels

A

small intestine obstruction

39
Q

where does a gallstone become lodged following cholecystoenteric fistula?

A

ileum

40
Q

after a car accident, persistent left shoulder pain, nausea, hiccups, hypotension, tachycardia, a bruise on left lower chest wall with tenderness, rigid abdomen

A

splenic laceration

41
Q

cause of congenital umbilical hernia

A

incomplete closure of the umbilical ring

soft, non-tender bulge at the umbilicus, protrudes with increased abdominal pressure, is reducible

42
Q

cause of congenital inguinal hernia

A

persistent processus vaginalis

43
Q

internal hemorrhoid venous drainage

A

superior rectal vein –> inferior mesenteric vein

44
Q

external hemorrhoid venous drainage

A

inferior rectal vein –> internal pudendal vein –> internal iliac vein

45
Q

dysphagia, odynophagia

endoscopic findings: patches of adherent, grey/white pseudomembranes on erythematous mucosa

A

candida albicans

46
Q

dysphagia, odynophagia
endoscopic findings: small vesicles –> punched out ulcers,
microscopic: eosinophilic intranuclear inclusions (Cowdry type A) in multinuclear cells

A

HSV1

47
Q

how do toxins responsible for C.difficle colitis damage intestinal mucosal cells

A

disrupt actin cytoskeleton and intracellular signaling

48
Q

long term supplementation with what is required after a gastrojejunostomy?

A

iron

49
Q

older male, with groin hernia. content protrudes out through Hesselbach triangle. Pathophysiology?

A

weakness of transversalis fascia

50
Q

woman with groin hernia, content protrudes through femoral ring

A

weakness of proximal femoral canal

51
Q

best prognostic indicators of liver function

A

serum albumin, bilirubin and PT

52
Q

indicators of impaired liver biosynthetic capacity

A

high PT, hypoalbuminemia

53
Q

indicators of impaired liver transport and metabolic capacity

A

high bilirubin

54
Q

what results from gene mutations that render trypsin insensitive to cleavage inactivation?

A

hereditary pancreatitis

55
Q

why are pancreatic enzymes (trypsin) secreted in inactive form

A

protect the pancreas from autodigestion

56
Q

microbes that produce toxins that inhibit 60S ribosomal subunit blocking protein synthesis and preventing tRNA binding which causes intestinal mucosal cell death and direct toxicity to renal epithelial cells

A
  • Enterhemorrhagic E.coli

- Shigella dysenteriae

57
Q

what do Ladd (fibrous) bands connecting the retroperitoneum in the RLQ to the right colon/cecum by passing over/compressing the duodenum indicate?

A

midgut malrotation

58
Q

what is necessary for infection with HDB

A

co-infection or superinfection of HBV

59
Q

effect of cirrhosis on BUN

A

decreased (ammonia cannot be efficiently converted to urea)

60
Q

effect of ammonia accumulation on inhibitory and excitatory neurotransmitters

A
  • increased GABA

- decrease glutamate and catecholamines

61
Q

fatigue, pruritus, hepatomegaly, and elevated alkaline phosphatase.
Liver biopsy: dilated bile canaliculi with green-brown plugs and yellowish-green accumulations of pigment within the hepatic parenchyma. diagnosis?

A

cholestatic liver disease

complications: fat-soluble vitamin deficiencies

62
Q

MOA of histamine on parietal cells in stomach

A

binds H2 receptors –> increase intracellular cAMP –> activated protein kinases –> increased transport of H+ by H/K ATPase into gastric lumen

63
Q

what type of intestinal cells does Shigella invade

A

microfold (M) cells in ileal Peyer patches

64
Q

kidney stones associated with Crohns

A

calcium oxalate stones (reduced intestinal formation of calcium oxalate, increased absorption of free oxalate)

65
Q

what decreases in proportion to an increase in bicarbonate in pancreatic secretions?

A

chloride

66
Q

diagnosis? severe epigastric abdominal pain and vomiting after an episode of binge drinking. four weeks later found to have a palpable upper abdominal mass and a visualized cystic lesion of CT

A

pancreatic pseudocyst

67
Q

what are the walls of psudeocyst made up of?

A

granulation tissue and fibrosis

68
Q

what cells are destroyed when the gastric antrum is colonized by H/pylori, causing duodenal ulcers

A

Delta cells (that produce somatostatin)

69
Q

effect of decreased somatostatin

A

increased gastrin

70
Q

MOA of duodenal ulcer formation caused by H.pylori colonizing the gastric antrum

A

increased gastric acid production

71
Q

MOA of gastric ulcer formation caused by H.pylori colonizing the gastric body (corpus)?

A

direct mucosal damage caused by bacterial products (ammonia, cytotoxins) and the resultant inflamamtory response

72
Q

what diseases are characterized by biopsy: lymphocytic infiltration with destruction of intrahepatic bile ducts

A

primary biliary cholangitis (PBC) and graft-vs-host disease (GVHD)