Inflammatory bowel disease in a child Flashcards

1
Q

How has the incidence of IBD in children changed?

A

Increased in last 20 years - could be interplay between genetics, microbiome and mucosal immunity

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2
Q

Is Crohn’s or UC more common?

A

Crohn’s more common in children (opposite in adults).

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3
Q

Name 3 general effects of IBD on children.

A
  • Poor general growth
  • Growth restriction
  • Adverse effects on psychological well-being
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4
Q

What is a typical presentation of Crohn’s disease?

A
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5
Q

What can Crohn’s be mistaken for in childhood?

A
  • Psychological problems
  • Anorexia nervosa
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6
Q

What do investigations show in Crohn’s disease?

A
  • Raised inflammatory markers (platelets, CRP, ESR)
  • Iron deficiency anaemia
  • Low serum albumin

Imaging:

  • Endoscopy and biopsy - diagnostic
  • CT/MRI - narrowing, fissuring and mucosal irregularities with bowel wall thickening
  • Remission with nutritional therapy
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7
Q

Define Crohn’s disease. Which part of bowel is usually affected?

A

A transmural, focal, subacute or chronic inflammatory disease, most commonly affecting the distal ileum and proximal colon.

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8
Q

What can be a complication of acutely inflamed, thickened bowel in Crohn’s?

A

Strictures of the bowel and fistulae may develop between adjacent loops of bowel or between bowel and organs (e.g. vagina and bladder)

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9
Q

What is the histological hallmark of Crohn’s disease?

A

Non-caseating epithelioid cell granulomata, although this is not identified in up to 30% at presentation.

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10
Q

How is remission induced with nutritional therapy in Crohn’s disease?

A

Nutritional therapy - normal diet is replaced by whole protein modular feeds (polymeric diet) for 6-8 weeks. Effective in 75% of cases.

Systemic steroids if this is ineffective

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11
Q

How is relapse managed in Crohn’s disease?

A

Immunosuppressant medication - azathioprine, mercaptopurine or methotrexate; almost always required to maintain remission

Biologics - anti-TNF (infliximab, adalimumab) when conventional treatments have failed

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12
Q

How can growth failure be corrected in Crohn’s?

A

Overnight nasogastric or gastrostomy feeds

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13
Q

What complications may require surgery in Crohn’s?

A
  • Obstruction
  • Fistulae
  • Abscess formation
  • Severe localised unresponsiveness to medical treatment often manifesting as growth failure
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14
Q

What is the prognosis in Crohn’s disease?

A

Usually good in childhood and may lead normal lives, with occasional relapses

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15
Q

Define ulcerative colitis.

A

Recurrent, inflammatory and ulcerating disease involving the mucosa of the colon

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16
Q

What is a typical presentation of UC?

A
  • rectal bleeding
  • diarrhoea
  • colicky pain
  • weight loss/growth failure (less frequently than in Crohn’s)
  • erythema nodosum
  • arthritis
17
Q

What is shown here?

A

erythema nodosum

seen in both Crohn’s and UC

18
Q

What is the pattern of inflammation in UC?

A

Extends from the rectum proximally for a variable length - 90% of children have pancolitis (not just confined to the distal colon like in adults)

19
Q

How is diagnosis of UC made?

A

Endoscopy (upper and ileocolonoscopy) and histological features

20
Q

What is seen on histology in UC?

A
  • mucosal inflammation
  • crypt damage (cryptitis, architectural distortion, abscesses, crypt loss)
  • ulceration
21
Q

What investigations are done for UC?

A

Bloods:

-

Imaging/invasive:

  • Endoscopy and biopsy - excludes infectious causes of colitis
  • Imaging - excludes extra-colonic inflammation present in Crohn’s disease
22
Q

What is used for induction and maintenance of remission in UC? What other treatments are available?

A
  • Aminosalicylates e.g. mesalazine
  • Immunomodulatory therapy, e.g. azathioprine alone to maintain remission or in combination with low-dose corticosteroid therapy.

Biological therapies such as infliximab or ciclosporin in patients with resistant disease

If ineffective, surgery should not be delayed.

23
Q

What is the use for steroids in UC?

A

Topical steroids - only used in disease confined to the rectum and sigmoid colon (which is rare in children)

Systemic steroids - used in aggressive/extensive disease for acute exacerbations.

24
Q

How is severe fulminating UC managed?

A

Medical emergency and requires IV fluids and steroids. If this fails, ciclosporin may be used.

Colectomy with an ileostomy or ileorectal pouch for severe fulminating disease (may be complicated by a toxic megacolon)

25
Q

The risk of which cancer is increased in UC?

A

Increased incidence of adenocarcinoma (1 in 200 risk for each year between 10-20 years from diagnosis)

Regular colonoscopic screening is done 10 years post-diagnosis .