IBD Flashcards

1
Q

Define Inflammatory Bowel Disease. What are 3 types?

A

chronic relapsing idiopathic inflammation of the
gastrointestinal tract

Ulcerative colitis

Crohn’s disease

Indeterminate colitis

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2
Q

Describe the epidemiology of IBD. Describe teh incidence, prevalence, racial incidence, ethnic incidence, gender incidence, age at onset, and association with tobacco use of ulcerative colitis and crohns disease.

A

prevalence varies widely
throughout the world (>1
million in the US)

•as countries become more
developed, incidence of IBD
increases

second most common
chronic inflammatory
disorder after RA

Incidence (per 100,000)
UC:2-10
CD:1-6

Prevalence (per 100,000)
UC: 35-100
CD:10-100

Racial incidence
Caucasians = African American

Ethnic incidence
High in Jews

Gender
Male = Female

Age at onset
15-25 (? 55-65)

Tobacco
UC: More in non/previous
smokers
CD: More in smokers

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3
Q

What are 3 factors involved in the pathogenesis of IBD?

A

idiopathic disorder, mechanism not well understood

combination of

immunologic abnormalities

genetic susceptibility

environmental factors

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4
Q

Describe what immunologic abnormalities occur in IBD. Describe this on a cellular basis. What is the difference in the pathogen. of CD and UC?

A

the mucosal immune system responds against ingested
pathogens but is unresponsive to normal intestinal microflora

•IBD: disrupted mucosal immune system leading to

defects in epithelial barrier function

unregulated and exaggerated immune response against
normal flora

consequence of too much T-cell activation and/or too
little control by regulatory T lymphocytes.

Cellular Basis: antigenic triggers and intrinsic factors activate T-cells in lamina propria  exaggerated immune response  inflammation and epithelial damage

  • differentiation of type 1 helper T cells (Th1)  CD
  • differentiation of type 2 helper T cells (Th2)  UC
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5
Q

Describe some environmental factors involved in IBD

A

development of colitis in murine models does not occur
when they are maintained in a germ-free environment,
but develops rapidly when these mice are colonized by
commensal bacteria

some antibiotics can be helpful in Crohn’s disease

  • improved sanitation is related to increased incidence of IBD
  • smoking is associated with higher risk for CD

•CLIMATE
–IBD more common in cold climates

•INDUSTRIALIZED NATIONS
–IBD more common in industrialized nations

  • NSAIDS
  • DIET?
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6
Q

What is the inflammation of CD like? Where can it occur? Where is the most common site? Describe the classic histopathologic features of CD.

A

inflammation is transmural

•any part of the GI tract may be
involved

•most common site terminal ileum,
ileocecal valve and the cecum

•sharp demarcation between
involved and uninvolved regions
•skip lesions: intervening normal
bowel between involved segments
•Focal mucosal ulcers which
coalesce later on to form long,
serpentine linear ulcers along the
long axis of the bowel
•with intervening uninvolved
mucosa between the ulcers: the
mucosa acquires a cobblestone
appearance
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7
Q

Describe some gross features of CD.

A
•transmural inflammation-->
–Ulcers progresse to fissures between
folds of the mucosa
–Extension of fissures → fistulas and
sinus tracts penetrating the serosa
•the intestinal wall becomes rubbery
and thick due to edema, fibrosis and
hypertrophy of muscularis propria
-->lumen narrowing “string sign”
(strictures) and obstruction

•serosa: granular and dull gray

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8
Q

Describe the symptoms of CD. What is the timeline like? What triggers its? How do they compare to UC?

A

generally more subtle as compared to UC

•intermittent attacks or progressive continuous course

•Diarrhea
Fever
abdominal pain

asymptomatic periods in between

•reactivation can be associated with stress, infection
(CMV, C. diff), NSAID’s or smoking

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9
Q

Describe some complications of CD.

A
  • strictures
  • fistulas

•extensive involvement of small bowel:

protein losing enteropathy
weight loss
malabsorption of vit B12, bile salts (steatorrhea)
iron deficiency anemia
Surgery for 50% to 80% of CD patients
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10
Q

Describe the morphology of UC.

A

superficial ulcerative
inflammation limited to the
colonic mucosa and submucosa

always begins in the rectum,
extends proximally in a
continuous fashion (no skips)
then abruptly stops with a clear
demarcation between involved
and uninvolved areas

the small intestine is normal

mucosa: red, granular, friable and easy to
bleed with superficial broad based ulcers
no mural thickening or stricture

Progressive mucosal atrophy–> flattened and
attenuated mucosal surface

the repeated cycle of ulceration,
alternating with the deposition of
granulation tissue during the healing
phase -->raised areas of inflamed tissue
(not neoplastic): pseudopolyps

•serosal surface is completely normal

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11
Q

Describe the presentation and symptoms of UC.

A

relapsing disorder: episodes of lower abdominal pain, cramps and
bloody mucoid diarrhea persisting for variable period of time
followed by asymptomatic intervals

25% of patients present with constipation (proctitis)

severity at first presentation:

60% mild

30% moderate

10% severe/fulminant

30% patients require colectomy due to uncontrollable disease

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12
Q

How common is toxic megacolon in UC? Desscribe it and its presentation.

A

Toxic Megacolon: 5%

•colonic distension of >6 cm

signs of systemic toxicity

Usually during fist 3 months of
diagnosis

inflammatory mediators damage
the muscularis mucosa and disturb
neuromuscular function

significant risk of perforation

surgery needed in 50% of cases

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13
Q

List 2 opthalmic, 2 dermatologic, 3 musculoskeletal, 1 liver, and 1 oral manifestation of IBD

A

Ophthalmic:
Anterior uveitis
Episcleritis

Dermatologic
Erythema Nodosum
Pyoderma Gangrenosum

Muskulosceletal
Migratory polyarthritis
Sacroiliitis
Ankylosing spondylitis

Liver: PSC (primary sclerosing polyangiitis)

Aphthous ulcer (canker sores)

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14
Q

What is the incidence of colorectal cancer in IBD pts? What are 5 risk factors?

A

the cumulative incidence of colorectal cancer in ulcerative/
Crohn’s colitis patients is 5% - 13%

risk factors:

extent of disease
duration ( >10 years)
activity
PSC
family history of colon cancer
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15
Q

Review mediations

A

Review Medications

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