Small Intestine Flashcards

1
Q

What are the 3 mechanisms of malabsorption

A

Structural disorder
Mucosal disorder
Abnormal luminal digestion

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2
Q

What are the general clinical features of malabsorption

A
Malaise
Anorexia 
abdominal bloating
diarrhoea 
weight loos
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3
Q

What are some specific clinical features of malabsorption

A

Steatorrhoea (fat malabsorption)
Oedema ascites (protein malabsorption)
Skin rash (Zn or Vit B malabsorption)
Cheilitis, glossitis (vitamin B malabsorption)
Neuropathy, psychological effects (vit B12 malabsorption)
Night blindness (vit A malabsorption)
Bruising (vit K or vit C malabsorption)
Bone pain, myopathy, oesteoporosis (vit D malabsorption)

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4
Q

What are the 3 aims of investigating malabsorption

A

To establish the condition
To identify the site of abnormality
To identify the severity

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5
Q

What is short bowel syndrome

A

This is typically when there is

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6
Q

When does short bowel syndrome occur

A

When there is insufficient functioning small intestine to allow normal digestion and absorption

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7
Q

What are some causes of short bowel syndrome (intestinal failure)

A
Extensive surgery 
Crohn's disease
Mesenteric ischaemia 
Radiation damage 
Volvulus 
Congenital abnormalities in children
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8
Q

What is the short term management of SBS

A

Correct malnutrition

Reduce gut secretions (PPI, codeine, loperamide)

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9
Q

What is the long term management of SBS

A

Monitor nutrition and ensure adequate calorie intake
Monitor hydration status
Replace vitamins and mineral
Reduce gut secretions
Treat small intestinal bacterial overgrowth
Cholecystectomy if gallstones develop
Small bowel transplantation

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10
Q

What is Ceoliac disease

A

An immune mediated disorder resulting in small intestinal villous atrophy which resolves on gluten withdrawal from the diet

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11
Q

What is the main toxic antigenic component of fluten

A

Alpha - gliadin

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12
Q

What does the protein in gluten cause

A

A T cell mediated inflammatory response of the small bowel

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13
Q

What is the prevalence of Coeliac disease in the UK

A

1:200

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14
Q

What are clinical features of Coeliac disease

A
Failure to thrive at weaning time (infants) 
Abdominal pain / bloating 
Lethargy
Anaemia
Diarrhoea or constipation
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15
Q

What is Coeliac disease linked to

A

HLA-DQ2

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16
Q

What is coeliac disease often linked to

A

Other autoimmune diseases such as dematitis herpetiformis, insulin dependent diabetes, thyroid disease, primary biliary cirrhosis

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17
Q

What are the investigations to confirm the fiagnosis

A

Duodenal biopsy is GOLD STANDARD

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18
Q

What would be seen on a duodenum biopsy in someone with Coeliac disease

A

Villous atrophy
Crypt hyperplasia
Intraepithelial lymphocytosis

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19
Q

What antibody needs to be tested for in Coeliac disease

A

IgA antibodies to Tissue transglutaminase (TTG)

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20
Q

Why might a patient get a false negative result for IgA

A

IgA deficiency

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21
Q

What should be tested when investigating the consequences of Coeliac disease

A

FBC and blood film
Haematinincs
Clotting screen
Bone investigation

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22
Q

What is the management for Coeliac Disease

A

Life long gluten-free diet to prevent the ongoing antigen provocation of the inflammatory response
Correct deificencies
Aggressive management of any bone disease

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23
Q

What is tropical sprue

A

A rare condition associated with small intestine villous atrophy and is thought to be post-infectious.

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24
Q

Who does tropical spruce normally affect

A

Residents of tropical countries (not travellers)

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25
Q

What are 2 common symptoms of tropical sprue

A

Diarrhoea and abdominal distension

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26
Q

What is the treatment for Tropical sprue

A

Longterm tetracycline and folic acid

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27
Q

What 3 things does colonisation of the small intestine by colonic flora result in

A

Deconjugating bile salts (diarrhoea)
Metabolising vitamin B12 (anaemia)
Metabolising carbohydrate (resulting in calorie malnutrition and halitosis)

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28
Q

What 2 investigations are carried out for the condition of small intestinal bacterial overgrowth?

A

Jejunal aspirate

Hydrogen breath test after ingesting glucose or lactulose

29
Q

How is the cause of small intestinal bacterial overgrowth investigated

A

Small bowel radiology (identifies structural or communication abnormalities )

30
Q

What is a complication of Small intestinal bacterial overgrowth investigated

A

Low B12 and normal folate

31
Q

What 3 things are required in the management of small intestinal bacterial overgrowth

A

Antibiotics directed towards colonic flora
Replace vitamin B12
Definiteive treatment if poosible - surgery or prokinetics

32
Q

What is bile acid malabsorption characterised by

A

Postprandial diarrhoea due to osmotic effect of bile salts in the colon or steatorrhoea

33
Q

If bile acid malabsorption is a secondary abnormality, what is it most commonly due to

A

Crohn’s disease
ileal resection
intestinal failure

34
Q

What is teh treatment for bile acid malabsorption

A

Cholestyramine - a bile acid sequestrant

35
Q

What is Whipple’s disease

A

A rare disease characterised by malabsorption, finger clubbing, fevers, skin pigmentation, seronegative large-joint arthropathy

36
Q

How is the diagnosis of Whipple’s disease established

A

By identifying foamy fmacrophagses which stain positive with periodic acid-Schniff on jejunal biopsy

37
Q

What is the treatment for Whipple’s disease

A

Cotrimoxazole or tetracycline for 1 year

38
Q

What is protein-losing enteropathy

A

Gut loss of protein sufficient to reduce serum albumin

39
Q

How common are small intestine tumours

A

Very rare - account for

40
Q

What are the 2 important types of small intestine tumours

A

Carcinoid and lymphoma

41
Q

Describe carcinoid tumours

A

Slow growing and arise from the appendix, small intestine or rectum

42
Q

When does carcinoid syndrome occur

A

Only if the tumour metastasises

43
Q

What is carcinoid syndrome caused by

A

Systemic release of serotonn, prostaglandins and bradykinins

44
Q

How are carcinoid tumours diagnosed

A

By measuring urinary 5-HIAA

45
Q

What is the treatment for carcinoid tumours

A

Surgical resection

46
Q

What are 3 main presentations of carcinoid syndrome

A

Wheezing
Flushing
Diarrhoea

47
Q

What is the diagnostic test for lymphoma

A

Abdominal CT

48
Q

What is the treatment of choice for lymphoma

A

Surgical resection

49
Q

What is immunoproliferative small intestinal disease

A

A rare condition also known as alpha heavy chain disease

50
Q

Who does immunoproliferative small intestinal disease normally affect

A

Mediterranean and Arab races

51
Q

How do patients with immunoproliferative small intestinal disease typically present

A

With diarrhoea
malabsorption
clubbing
weight loss

52
Q

What shows the alpha heavy chains in immunoproliferative small intestinal disease

A

Serum electrophoresis

53
Q

What is the treatment for immunoproliferative small intestinal disease

A

Long term antibiotics

Only some need chemotherapy

54
Q

What is more common: single polyp or multiple polyps

A

Multiple polyps

55
Q

What are the 3 types of multiple polyps

A

Nodular lymphoid hyperplasia
Hamartomas
Andeomatous

56
Q

What is chronic intestinal pseudo-obstruction

A

Refers to a dpectrum of rare disorders characterised by the signs and symptoms of intestinal obstruction in the absence of true obstruction

57
Q

What is required to determine the diagnosis of chronic intestinal pseudoobstruction

A

Radiological demonstation of a dilated proximal small bowel

58
Q

What is Meckel’s diverticulum

A

The commonest congenital gut abnormality resulting from failure to close the vitelline duct

59
Q

If a patient is symptomatic with Meckel’s diverticulum, at what age would they present?

A

Before the age of 2

60
Q

Males are twice as likely to be affected. True or False

A

True

61
Q

What are the classic symptoms of Meckel’s diverticulum

A

Painless melaena with intestinal obstruction or intussusception being rare

62
Q

How is Meckel’s diverticulum diagnosed

A

Using a Meckel’s scan - injecting a radioisotope which is taken up by ectopic parietal cells

63
Q

Who is most likely to have hypolactasia

A

Africans and Asians

64
Q

What might secondary causes of lactase deficiency result in

A

Osmotic diarrhoea, abdominal pain
borborygmi after eating milk products
Flatulence

65
Q

How is diagnosis of lactase deficiency made

A

Using a lactose substrate hydrogen breath test

66
Q

What is the treatment for lactase deficiency

A

Minimising milk products

67
Q

In food allergy, what type of hypersensitivity reaction occurs

A

Type 1

68
Q

What is the treatment for food allergy

A

Dietary avoidance