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25 Cards in this Set

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What is the normal Villous to crypt length ratio?
3-5 villous to 1 crypt length
What is the external layer of the small intestine?
serosal layer
How many IEL (lymphocytes) are present in the small bowel normally?
There are less than 10 Intra Epithelial Lymphocytes/ 100 epithelial cells
What structure is only present in the duodenum of the small bowel?
Brunner's glands
What structure is only present in the ileum of the small bowel?
Peyer's patches (lymphoid follicles)
Celiac Disease

Symptoms
Abdominal pain

Diarrhea

Steatorrhea

Dermatitis herpetiformis (vesicular lesion on abdomen... cutaneous disease)

Fatigue (lack of energy due to lack of nutrients from food)
Celiac Disease

Pathology
An immune – mediated disorder in genetically susceptible hosts with damage to SI mucosa & malabsorption

2 or more genes involved: class I HLA-B8 & class II HLA-DR3 & DQW2

Exposure to gliadin results in humoral & cell mediated injury (CD8+ cells, lymphocytes, Abs)

Possible relationship to prior infection with adenovirus I2

E1B viral protein homologous with gliadin possibly resulting in cross reactivity

Serum endomysial and tissue transglutaminase autoantibodies
Celiac Disease

Epidemiology
Worldwide in distribution

Occurs mostly in European whites

Clinical onset anytime from infancy to late adulthood
Which HLA phenotypes predispose you to Celiac Disease?
2 or more genes involved: class I HLA-B8 & class II HLA-DR3 & DQW2
Gliadin
is a component of the gluten portion of wheat
What is the treatment for Celiac Disease?
Gluten free diet... allows absorption and histology to return to normal
What happens to the mucosa in celiac disease?
the luminal surface is flat because of atrophy and blunting of villi

crypt hypertrophy

overall thickness of the mucosa is not changed

increased lymphocytes within the epithelium (much more than 10 IES/100 epithelial cells

espansion by plasma cells
Refractory Sprue
Absent or incomplete clinical response to gluten free diet
Abnormalities in T cells in many patients with loss of CD4 & CD8 & with monoclonal rearrangements in TCR gamma gene

Early T cell lymphoma (may indicate an early form of cancer)

A subset of pts with refractory sprue develop collagenous sprue
What is the most common intestinal parasite in US?
Giardia
Clinical Presentation of Giardiasis
More common in children

Abrupt or gradual onset of diarrhea

More severe and protracted with underlying immunodeficiency (renal transplants, AIDS) or malnutrition
How do you get Giardia lamblia?
infects via ingestion of water or food contaminated by CYSTS
Giardiasis

Histology
At higher magnification there are eosinophilic (pink) triangles that create a blockade to stop absorpion

Do not invade mucosa
Crohn's Disease

Epidemiology
Worldwide distribution
- More common in western nations

In US, incidence is rising; 8/100,000

Genetic susceptibility

Most often presents in 2nd decade

2nd smaller peak in 8th decade
Crohn's Disease

Pathology
Thickened wall with firm, stiff consistency due to fibrosis (and scarring of submucosa), muscular hypertrophy & fat wrapping

Strictures (result of wall thickening)

Fistulas
In early or mild disease, mucosa has aphthous ulcers

With progression, fissures (small based linear hole that can make fistula with adjacent sxr) or wide based longitudinal ulcers; cobblestone mucosa (due to edema and scaring)

Skip areas (healthy tissue between dzed tissue)
Crohn's Disease

Symptoms
RLQ pain

crampy

no hematemesis
How do you cure Crohn's disease?
you cannot cure it

you can treat it
Aphthous Ulcer
small shallow ulcer
What does a pathologist look for on a surgically resected specimen for crohn's disease?
1. transmural chronic inflammation

2. Fibrosis (esp. in submucosa)

3. Non-caseating granulomas
Non-caseating granulomas of small bowel make you think of what in US? in other countries?
In US, Crohn's Disease

In other country, Tuberculus bovium.
Histopathology of Crohn’s Disease
- Transmural chronic inflammation with lymphoid nodules (string of beads)
- Fibrosis
- Muscular & neuronal (myenteric plexus) hypertrophy
- Basilar plasmacytosis
- PMNs in lamina propria & epithelium (cryptitis)
- Ulcers, including fissures
- Pseudopyloric metaplasia
- Non-necrotizing granulomas
- (biopsies 30%; resections 60%)
- Vasculitis
- Variability in changes