Vomiting and malabsorption 2 (bilious vom & coeliac) Flashcards

1
Q

What is billious vomiting?

Why does it occur?

A

Vomiting with bile in it

Occurs when there is intestinal obstruction - ie obstruction further down than the 2nd part of the duodenum (beyond the hepatopancreatic ampulla)

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2
Q

Is bilious vomiting bad?

What are the causes of it?

A

Yeah pretty bad

Intestinal atresia (newborns)

Malrotation +/- volvulus

Intussusception

Ileus

Crohn’s w strictures

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3
Q

What is meant by malrotation +/- volvulus?

A

Intestinal malrotation is a congenital anomaly of rotation of the midgut

It can lead to Volvulus - which is when the intestine twists around itself and the mesentery that supports it - leading to obstruction

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4
Q

What is intussusception?

A

When part of the intestine folds into the section immediately ahead of it

like dis

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5
Q

What is an ileus?

A

When the intestines dont do the peristalsis business as they should be

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6
Q

What investigations and treatments are avaliable in the case of intestinal obstruction

A

Abdominal xray

Contrast meal

Surgical re-exploratory laparotomy

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7
Q

In the context of water usage by the GI tract…

How much:

a) enters the duodenum
b) is lost in the colon
c) is lost in the faeces

A

a) 9L enters duodenum
b) 1.5L enters colon
c) <200ml lost in poo

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8
Q

Define acute, persistent and chronic diarrhoea

A

4 or more stools per day for:

<1 week - acute

2-4 weeks - persistent

4 or more weeks - chronic

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9
Q

What are the groups of causes of diarrhoea in yungers

A

Motility disturbance, secretory abnormalities & malabsorption (osmotic)

Motility disturbance:

  • toddler diarrhoea
  • IBS

Acute secretion (secretory):

  • acute infective diarrhoea
  • IBD

Malabsorption (osmotic):

  • allergies
  • coeliac disease
  • cystic fibrosis
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10
Q

Describe how secretory diarrhoea occurs

A

Classically associated with toxin production from Vibrio cholerae and enterotoxigenic Escherichia coli

These toxins cause intestinal fluid secretion - predominantly driven by active Cl- secretion via CFTR

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11
Q

Give an overview of the clinical approach to a child with chronic diarrhoea

A

History

Growth & weight gain

Faeces analysis

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12
Q

What aspects of history are important in a child with chronic diarrhoea?

A

Age at onset

Gradual or sudden onset

Family history

Travel history / local outbreaks

Nocturnal defecation - v suggestive of organic pathology

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13
Q

For a child presenting with chronic diarrhoea - describe what faecal analysis is?

A

Appearance

Stool culture

Differentiation between secretory vs. osmotic

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14
Q

Describe how osmotic and secretory diarrhoea are differentiated between

Describe how the values on the table would relate to each other (obvs dont care about the actual numbers really)

A

Osmotic diarrhoea is relatively low in volume and very much food dependant (ie when the child stops eating, diarrhoea soon stops too)

Secretory diarrhoea is very high volume and happens regardless of food intake (bc its not really to do with food)

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15
Q

What are the conditions that cause fat malabsorption (leading to diarrhoea)?

A

Pancreatic disease - insufficient lipase production leads to steatorrhoea/diarrhoea:

  • cystic fibrosis
  • Schwachan-diamond syndrome

Hepatobiliary disease:

  • chronic liver disease
  • cholestasis
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16
Q

Wee bit of revision - What are the main features of cystic fibrosis?

A

Neonatal period:

  • meconium ileus
  • less commonly prolonged jaundice

Malabsorption:

  • steatorrhoea
  • failure to thrive

Recurrent chest infections

Liver disease

Absent vas deferens

17
Q

What is Schwachman-diamond syndrome?

A

rare congenital disorder characterized by:

exocrine pancreatic insufficiency

bone marrow dysfunction (esp neutropenia)

skeletal abnormalities

short stature

18
Q

What is coeliac disease?

What mutations is it associated with?

What ingredients cant the coeliac people eat?

A

Autoimmune condition characterised by gluten-sensitive enteropathy

HLA-DQ2 - and - HLA-DQ8

Wheat, rye and barley

19
Q

What are the features of coeliac disease?

A

Abdominal bloatedness (pot belly)

Diarrhoea

Failure to thrive, short stature, skinny

Lethargy

Persistent N&V

Dermatitis herpetiformis

20
Q

What conditions is coeliac disease associated with?

A

Type 1 diabetes (IDDM)

Autoimmune thyroid disease

Dermatitis herpatiformis

Autoimmune disease in First degree relatives v important

21
Q

Describe how coeliac disease is screened for

A

If suspicion of coeliac disease…

Serological screens:

  • TTG antibodies (anti-tissue transglutaminase) (IgA)
    • if +ve - endomyseal antibody (IgA)
  • Serum IgA

Genetic testing

  • HLA-DQ2
  • HLA-DQ8

Duodenal biopsy - if indicated

22
Q

When is duodenal biopsy indicated for coeliac investigation?

A

If all of the following are present - no need to biopsy:

  • Symptomatic children
  • Anti TTG >10 times upper limit of normal
  • Positive anti endomysial antibodies
  • HLA DQ2, DQ8 positive

If any of them are not present - then biopsy is indicated

23
Q

What are the findings on a duodenal biopsy in coeliac disease?

What is the appearance of the duodenum on the actual endoscopy?

A

villous atrophy

crypt hyperplasia

increase in intraepithelial lymphocytes

lamina propria infiltration with lymphocytes

On endoscopy:

Smooth, erythematous mucosa

Oedema

24
Q

How is coeliac disease treated?

A

Gluten-free diet for life

Gluten must not be removed prior to diagnosis as serological and histological features will resolve

In very young <2yrs, re-challenge and re-biopsy may be warranted

25
Q

If coeliac disease is untreated - what risk does the patient face?

A

Increased risk of rare small bowel lymphoma in untreated

I assume in the peyers patches or something like that

26
Q

Dunzo

A