GI Pathology III: Small Intestine Flashcards

1
Q

What are the clinical features and histological findings in Hirschsprung disease?

A

Constipation with lack of ganglion cells on histology

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2
Q

What is the infectious agent in pseudomembranous colitis?

A

C. difficile

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3
Q

What is the common parasitic infection that presents with bloody diarrhea?

A

E. histolytica

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4
Q

What is the gene mutation in familial adenomatous polyposis (FAP)?

A

Autosomal dominant mutation of the APC gene

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5
Q

Plicae Circularis

A

Plicae circularis are folds of the mucosa and submucosa

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6
Q

Paneth Cells

A

Function in cell defense in the intestine. Paneth cells have lysozymes and defensins.

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7
Q

What are features specific to the duodenum?

A

Brunner’s Glands

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8
Q

What are features specific to the ileum?

A

Peter’s Patches

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9
Q

What is the main function of the large intestine?

A

Absorption of water

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10
Q

Where is Meissner Plexus located?

A

In the submucosa

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11
Q

Where is Auerbach’s Plexus located?

A

Between the circular and longitudinal muscle in the muscularis propria

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12
Q

Intussusception

A

Telescoping of bowel segment into distal segment often at the ileocecal junction

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13
Q

Volvulus

A

Twisting of the bowel around its mesentery leading to obstruction and can compromise blood flow

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14
Q

Where does volvulus occur in children? Adults?

A

Children - midgut

Adults - sigmoid

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15
Q

Necrotizing Entercolitis

A

Most common GI emergency in premature neonates with acute necrotizing inflammation of the small and large bowels

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16
Q

Meckel’s Diverticulum

A

Disease of 2’s

  • 2:1 male to female
  • 2 major complications are pain with inflammation and hemorrhage with ulcer
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17
Q

Who is most affected by Hirschsprung disease?

A

Males in a 4:1 ratio

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18
Q

What is Hirschsprung disease associated with?

A

Down syndrome

19
Q

What can pancreatic insufficiency be caused by and what does it result in the malabsorption of?

A
  • Pancreatitis/Cancer

It will affect the absorption of fat and vitamins A, D, E and K

20
Q

What is the most common type of disaccharide deficiency and what are the symptoms?

A

Lactase. Osmotic diarrhea.

21
Q

Abetalipoproteinemia

A

Decreased synthesis of apolipoprotein B which decreases the amount of chylomicrons leading to the accumulation of fat and cholesterol in the enterocytes - presents as failure to thrive

22
Q

Celiac Disease

A

Autoimmune disorder that results in the damage of small intestinal lining when gluten is eaten

23
Q

Who is celiac disease seen most often in?

A

Caucasians and Europeans

24
Q

What is the pathogenesis of celiac disease?

A

Gluten is converted to gliadin which is deaminated by TTG and is presented to a T cell. The T cell will attack the enterocytes and activate B-cells leading to Ab formation

25
Q

What happens to the villi in celiac disease?

A

They are lost from the inflammation

26
Q

What are the prominent cells seen in celiac disease?

A

CD8+ T cells

27
Q

What are the important tests for celiac disease?

A
  • Serologic test for TTG and gliadin Ab

- Biopsy showing villous atrophy

28
Q

What are some bacterial causes of enterocolitis?

A
  • Cholera
  • Campylobacter
  • Yersinia
  • E. coli
  • Shigella
  • Salmonella
29
Q

What are some viral causes of enterocolitis?

A
  • Norovirus

- Rotavirus

30
Q

What are some of the parasitic causes of enterocolitis?

A
  • Nematodes
  • Flatworms
  • Protozoans (Giardia, E. histolytica)
31
Q

What is the histological characteristic of E. histolytica infection?

A

Flask shaped ulcer

32
Q

What is the histological finding in pseudomembranous enterocolitis?

A

Mushroom pseudomembrane

33
Q

Who is generally affected by collagenous enterocolitis?

A

Middle to older age women

34
Q

What is the histological finding of collagenous enterocolitis?

A

Presence of collagen (blue with trichrome stain)

35
Q

What is lymphocytic enterocolitis associated with?

A

Autoimmune diseases

36
Q

What will be seen on histology of lymphocytic enterocolitis?

A

Lymphocytes

37
Q

Whipple Disease

A

Rare and found in men more commonly. It is caused by Tropheryma whippleli and is engulfed by macrophages where they fill the lamina propria and distend it.

38
Q

Crohn’s Disease

A

It is a disordered response to bacteria. Usually affects the terminal ileum but can affect any part of the GI tract and it will show with strictures and serosal creeping fat.

39
Q

What is seen on histology of Crohn’s disease?

A
  • Transmural inflammation - full thickness of the wall

- Ulceration and non-caseating granulomas

40
Q

Ulcerative Colitis

A

Autoimmune with relapsing attacks of bloody mucoid diarrhea with pain with diffuse continuous inflammation

41
Q

What layers does ulcerative colitis affect?

A

Only the mucosa and submucosa, and there are NO non-caseating granulomas

42
Q

What is the diarrhea of Crohn’s like?

A

Non-bloody

43
Q

What is the diarrhea of ulcerative colitis like?

A

Bloody

44
Q

What is a distinguishing feature in the how the intestines are affected in Crohn’s VS ulcerative colitis?

A

Crohn’s will have skip areas and thus is focal.

UC is continuous and therefore diffuse.