IBD: Ulcerative Colitis Flashcards

1
Q

What is ulcerative colitis (UC)?

A

A type of inflammatory bowel disease characterized by diffuse inflammation of the colonic mucosa and a relapsing, remitting course.

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2
Q

Briefly describe the macroscopic pathophysiology of UC

A

It is characterized by diffuse, continuous, superficial inflammation of the large bowel limited to the intestinal mucosa, and usually affects the rectum with a variable length of the colon involved proximally.

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3
Q

Briefly describe the microscopic pathophysiology of UC

A

UC usually involves only the mucosa, with the formation of crypt abscesses and a coexisting depletion of goblet cell mucin.

Further microscopic changes include inflammation of the crypts of Lieberkuhn and abscesses. Ulcerated areas are soon covered by granulation tissue.

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4
Q

Give examples of extra-intestinal manifestations of UC

A

Ulcerative colitis has a number of extra-intestinal manifestations including:

  • Uveitis
  • Inflammatory arthritis
  • Erythema nodosum
  • Pyoderma gangrenosum
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5
Q

What are the risk factors for UC?

A
  • Family history of IBD
  • HLA-B27
  • Infection
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6
Q

What are the signs of UC?

A
  • Malnurition
  • Extraintestinal manifestations (e.g. erythema nodosum and acute arthropathy)
  • Abdominal tenderness
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7
Q

What are the symptoms of UC?

A
  • Rectal bleeding
  • Diarrhoea
  • Blood in stool
  • Abdominal pain
  • Arthritis and spondylitis
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8
Q

What investigations should be ordered for UC?

A
  • Stool studies
  • FBC
  • Comprehensive metabolic panel (inclduing LFTs)
  • ESR
  • CRP
  • Abdominal radiograph
  • Flexible sigmoidoscopy
  • Colonoscopy
  • Biopsies
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9
Q

Why investigate stool studies? And what may this show?

A
  • Of all the stool inflammatory tests available, faecal calprotectin is recommended. It is elevated when there is bowel inflammation and correlates with endoscopic and histological gradings of disease severity.
  • Negative culture and Clostridium difficile toxins A and B; WBC present; elevated faecal calprotectin
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10
Q

Why investigate FBC? And what may this show?

A
  • Variable degree of anaemia, leukocytosis or thrombocytosis
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11
Q

Why investigate comprehensive metabolic panel (including LFTs)? And what may this show?

A
  • May show a variety of things:
    • Hypokalaemic metabolic acidosis
    • Elevated sodium and urea
    • Elevated alkaline phosphatase
    • Bilirubin
    • Aspartate aminotransferase (AST)
    • Alanine aminotransferase (ALT)
    • Hypoalbuminaemia
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12
Q

Why investigate ESR? And what may this show?

A
  • Marker for inflammation
  • Variable degree of elevation
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13
Q

Why investigate CRP? And what may this show?

A
  • Marker for inflammation
  • Variable degree of elevation
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14
Q

Why investigate using abdominal ragiograph? And what may this show?

A
  • Used to estimate of the extent of disease because an ulcerated colon usually contains no solid faeces
  • Dilated loops with air-fluid level secondary to ileus; free air is consistent with perforation; in toxic megacolon, the transverse colon is dilated to ≥6 cm in diameter
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15
Q

Why investigate using flexible sigmoidoscopy? And what may this show?

A
  • Note: findings are as in colonoscopy, but examination is limited to distal colon
  • Dilated loops with air-fluid level secondary to ileus; free air is consistent with perforation; in toxic megacolon, the transverse colon is dilated to ≥6 cm in diameter
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16
Q

Why investigate using colonoscopy? And what may this show?

A
  • Indicated in patients with UC who are not responding well to treatment, in order to rule out infections (particularly cytomegalovirus and Clostridium difficile) and assess the need for surgery
  • Rectal involvement, continuous uniform involvement, loss of vascular marking, diffuse erythema, mucosal granularity and fistulas (rarely seen)
17
Q

Why investigate using biopsies? And what may this show?

A
  • Biopsies should be obtained at the time of endoscopy even if the mucosa appears unremarkable. Biopsies are essential for diagnosis and differential diagoses.
  • Continuous distal disease, mucin depletion, basal plasmacytosis, diffuse mucosal atrophy, absence of granulomata and anal sparing