GATEOENTEROLOGY 1.2 (AB) Flashcards

1
Q

What is the gold standard diagnostic test for Hirschsprung Disease (Congenital Aganglionic Megacolon)?

A

Rectal suction biopsy

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2
Q

What developmental disorder is characterized by absence of ganglion cells in the submucosal and myenteric plexus?

A

Hirschsprung Disease (Congenital Aganglionic Megacolon)

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3
Q

What is the most common cause of lower intestinal obstruction in neonates?

A

Hirschsprung Disease

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4
Q

What is the incidence of Hirschsprung Disease?

A

1 in 5,000 live births

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5
Q

What is the male-to-female ratio in short-segment Hirschsprung Disease?

A

0.16736111111111107

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6
Q

What is the male-to-female ratio in total colonic aganglionosis?

A

~2:1

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7
Q

What is the pathophysiology of Hirschsprung Disease?

A

Arrested migration of neuroblasts causing absence of myenteric and submucosal plexus, leading to inadequate bowel relaxation and obstruction

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8
Q

What are the classic neonatal clinical manifestations of Hirschsprung Disease?

A

Distended abdomen, failure to pass meconium, bilious emesis, feeding intolerance

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9
Q

What neonatal conditions should Hirschsprung Disease be differentiated from?

A

Meconium plug syndrome, meconium ileus, intestinal atresia

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10
Q

What is the Currarino triad associated with older patients with Hirschsprung Disease?

A

Anorectal malformations, sacral bone anomalies, presacral anomaly

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11
Q

What are examples of anorectal malformations in Currarino triad?

A

Ectopic anus, anal stenosis, imperforate anus

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12
Q

What are examples of sacral bone anomalies in Currarino triad?

A

Hypoplasia, poor segmentation

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13
Q

What are examples of presacral anomalies in Currarino triad?

A

Anterior meningoceles, teratoma, cyst

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14
Q

What is intussusception?

A

Telescoping of one part of the intestine into an adjacent segment

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15
Q

What is the segment that invaginates called in intussusception?

A

Intussusceptum

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16
Q

What is the receiving segment called in intussusception?

A

Intussuscipiens

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17
Q

What is the most common cause of intestinal obstruction between 5 months and 3 years?

A

Intussusception

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18
Q

What is the most common abdominal emergency in children younger than 2 years?

A

Intussusception

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19
Q

What stool characteristic is pathognomonic for intussusception?

A

Currant jelly stool

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20
Q

What physical exam finding is characteristic of intussusception?

A

Sausage-like mass

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21
Q

What ultrasound finding is characteristic of intussusception?

A

Target sign

22
Q

What is the treatment for intussusception?

23
Q

What is peptic ulcer disease (PUD)?

A

Inflammatory condition caused by imbalance between cytoprotective and cytotoxic factors in stomach and duodenum

24
Q

What are the key factors in peptic ulcer disease pathogenesis?

A

Acid and pepsin (damage), mucosal defense failure

25
Q

What are the two types of peptic ulcers?

A

Primary (chronic, duodenal), Secondary (acute, stress-related)

26
Q

Where are gastric ulcers usually located?

A

Lesser curvature of the stomach

27
Q

Where do 90% of duodenal ulcers occur?

A

Duodenal bulb

28
Q

What is the main causative factor for mucosal injury in PUD?

A

Acid-pepsin activity

29
Q

What are examples of mucosal defense defects in PUD?

A

Impaired mucus-bicarbonate barrier, reduced prostaglandin synthesis, decreased mucosal blood flow

30
Q

What bacterial infection is a contributing factor for peptic ulcer disease?

A

Helicobacter pylori infection

31
Q

What medication class contributes to peptic ulcer disease by inhibiting prostaglandin synthesis?

32
Q

What symptoms are associated with peptic ulcer disease?

A

Epigastric pain, nausea, vomiting, hematemesis, melena

33
Q

What are severe complications of peptic ulcer disease?

A

Perforation, obstruction

34
Q

What is the causative agent of Helicobacter pylori gastritis?

A

Helicobacter pylori (Gram-negative, S-shaped rod)

35
Q

How is Helicobacter pylori transmitted?

A

Fecal-oral or oral-oral (e.g., kissing)

36
Q

What are key enzymes produced by Helicobacter pylori?

A

Urease, catalase, oxidase

37
Q

What gastric condition is commonly associated with H. pylori but often asymptomatic?

A

Chronic active gastritis

38
Q

What extragastric conditions can H. pylori infection cause?

A

Iron deficiency anemia, idiopathic thrombocytopenic purpura (ITP), short stature

39
Q

What malignancies are linked to H. pylori infection?

A

Gastric adenocarcinoma, MALT lymphoma

40
Q

What is the gold standard diagnostic method for H. pylori?

A

Endoscopy with biopsy

41
Q

What non-invasive test for H. pylori detects urease activity?

A

13C-Urea breath test

42
Q

What stool-based test is highly sensitive and specific for H. pylori, especially in children?

A

Stool antigen test

43
Q

What is the first-line eradication therapy for H. pylori?

A

Triple therapy: PPI + Amoxicillin + Clarithromycin for 14 days

44
Q

What is the recommended treatment for resistant H. pylori infection?

A

Quadruple therapy: PPI + Bismuth + Metronidazole + Tetracycline

45
Q

What medication should be discontinued 2 weeks before H. pylori testing to avoid false negatives?

46
Q

What classification does WHO assign to Helicobacter pylori?

A

Group I carcinogen

47
Q

What is the relative risk increase for gastric cancer in H. pylori-infected adults?

A

2.3 to 8.7 times higher

48
Q

How does urease contribute to H. pylori pathogenesis?

A

Converts urea to ammonia, neutralizing acid but damaging mucosa

49
Q

What are the invasive methods to diagnose H. pylori?

A

Endoscopy with biopsy, histologic exam with Giemsa stain

50
Q

What are the non-invasive methods to diagnose H. pylori?

A

13C-Urea breath test, stool antigen test