Coeliac Disease Flashcards

1
Q

Define coeliac disease

A

Inflammatory disease of SMALL COLON caused by intolerance to gluten, causing chronic intestinal malabsorption

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2
Q

Aetiology

A

Genetics - HLA-B8, DR3, DQW2
Sensitivity to gliadin component of gluten
Triggers immunological reaction in the small intestine, leading to mucosal damage and loss of villi

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3
Q

Epidemiology

A

1/2000 in UK
1/300 in west of Ireland
Rare in east asia

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4
Q

History/symptoms

A
Asymtomatic 
Abdo discomfort, pain, bloating 
Steatorrhoea/diarrhoea 
Tiredness, malaise, weight loss despite normal diet 
Failure to 'thrive' in children
Amenorrhoea in young adults
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5
Q

Which three genetic markers are associated with coeliac disease?

A

HLA-B8
DR3
DQW2

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6
Q

Explain the pathophysiology behind malabsorption

A

Sensitivity to gliadin component of gluten

triggers an immunological reaction in the small intestine, leading to mucosal damage and loss of villi

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7
Q

Signs

A

Anaemia - pallor
Malnutrition - short stature, abdo distention, wasted buttocks in children
Vitamin/mineral deficiencies e.g. osteomalacia, easy bruising
Dermatitis herpetiformis - Intense itchy papulovesiclualr blisters on extensors e.g. elbows, knees or buttocks
?clubbing

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8
Q

What would you look at as an indication of fat stores?

A

Triceps skinflap

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9
Q

Explain the pathophysiology behind dermatitis herpetiformis

A

Normally, gliadin is de-amidated by tissue transglutaminase (tTG), however there is often a cross reaction where the antibodies produced against tTG also bind to epidermal transglutaminase and thus cause these herpes-like blisters!

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10
Q

Initial investigations

A
FBC 
Serology
Stool culture
D-xylose test
Endoscopy
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11
Q

What would you look at in an FBC for coeliac disease?

A
  • low iron
  • low folate
  • low Hb
    U&Es
    Albumin (protein losing enteropathy)
    Calcium
    Phosphate
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12
Q

What serological tests would you conduct?

A
Tissue transglutaminase (TTG)
IgG anti-gliadin (AGA)
IgA and IgG anti-endomysial transglutaminase
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13
Q

What else must you do with serology?

A

Measure immunoglobulin levels as low IgA is common in coeliac disease

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14
Q

What percentage of people have an IgA deficiency?

A

1/50

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15
Q

Why do you do a stool test?

A

To exclude infection

To look at fat content (faecal fat tests for steatorrhoea)

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16
Q

Explain a D-xylose test

A

You give a pt oral xylose

If there is reduced urinary excretion, it suggests malabsorption

17
Q

What would endoscopy show?

A

Flat, smooth mucosa and villous atrophy in small intestine

18
Q

What would a biopsy show of the:

  • villi
  • crypt
  • epithelium
  • lamina
  • propria
A

Villous atrophy
Crypt hyperplasia of duodenum
Cuboidal appearance of epithelium (should be simple columnar)
Inflammatory infiltrate in lamina propria

19
Q

Management

A

Gluten avoidance
Avoid all types of wheat, rye and barley products

Vitamin and mineral supplements
Oral corticosteroids if disease does not subside with gluten withdrawal

20
Q

Complications

A

Iron, folate and B12 deficiency
Osteopenia/osteoporosis
Ulcerative jejunoileitis

Bacterial overgrowth
Rarely cerebellar ataxia
Small bowel lymphoma = EATL (enteropathy-associated T-cell lymphoma)

21
Q

Prognosis

A

With strict adherence to gluten-free diet, most patients make a full recovery.
Symptoms usually resolve within weeks. Histological changes may take longer to resolve. A
gluten-free diet needs to be followed for life.

22
Q

What might be seen on biopsy?

A

Villous atrophy
WBC infiltration
Cryptal hyperplasia

23
Q

Further investigations

A
Refer to:
Dietitians 
Biopsy 
Screening for first degree relatives 
Bone density scan
24
Q

What would you do if someone’s symptoms don’t improve with a gluten free diet?

A

Rerefer to dietitian to ensure diet is strictly adhered to

Repeat TTG/serology