21 Lower GI pathology Flashcards

1
Q

Describe diverticulosis of the colon.

Location?

A

Protrusions of mucosa and submucosa through the bowel wall.
Commonly in sigmoid colon.
Located between mesenteric + anti-mesenteric taenia coli.

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2
Q

What is the epidemiology of diverticulosis of the colon? (4)

A

Western, urban areas.
Related to fibre content in diet.
Increases with age.
Male = female.

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3
Q

What is the pathogenesis of diverticulosis of the colon?

A

Increased intra-luminal kPa (irregular peristalsis due to overlapping arcs in bowel wall).
Points of weakness in wall (penetration by arteries + age related connective tissue changes).

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4
Q

What is the pathology of diverticulosis? (4)

A

Thickening of muscular propria.
Elastosis of taeniae coli (shortening the colon).
Redundant mucosal folds.
Sacculation and diverticula.

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5
Q

What are the symptoms of diverticulosis?

Complications? (7)

A

Asymptomatic.
Diverticulitis, perforation, haemorrhage.
Obstruction, fistula, colitis, polypod prolapsing mucosal folds.

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6
Q

What are the acute classifications of colitis? (6)

A
Infective: campylobacter, salmonella, CMV.
Antibiotic associated.
Drug induced.
Acute ischaemic and radiation.
Neutropenic.
Phlegmonous (diffuse inflammation).
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7
Q

What are the chronic classifications of colitis? (8)

A
Chronic idiopathic IBD.
Microscopic.
Ischaemic.
Diverticular.
Chronic infective: amoebic + TB.
Diversion
Eosinophilic.
Chronic radiation.
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8
Q

What is the epidemiology of IBD?

age, sex, living, RFs (2)

A
20-40 years.
CD= 1.3F : 1M       UC Male=Female.
More UC in urban areas.
Oral contraceptive increases both.
Smoking: UC:0.5x CD:2x
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9
Q

How does IBD present? (8)

A
Diarrhoea - urgency/tenesmus.
Constipation, bleeding.
Abdo pain.
Anorexia.
Weight loss
Anaemia.
Palpable mass.
Oral ulcers if CD.
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10
Q

What are the complications of IBD? (5)

A
Toxic megacolon and perforation.
Haemorrhage.
Carcinoma.
Stricture (rare in UC, common in CD).
Short bowel syndrome in CD.
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11
Q

Where is Crohns disease commonly distributed? (3)

A

Ileocolic.
Small bowel.
Colonic.

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12
Q

What is the pathology of ulcerative colitis? (8)

Site. Appearance. Histology.

A
Affects colon, appendix, terminal ileum. 
Continuous. 
Rectum always involved. 
Granular and red. Normal serosa. 
Strictures rare. 
Mucosal. 
Crypt abscesses present with severe crypt distortion. 
Polyps common.
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13
Q

What is the pathology of Crohns disease? (10)

Site. Appearance. Histology.

A
Affects all of GI tract. 
Terminal ileum involved more than in UC. 
Anal fissures very common. 
Skip lesions. 
Cobblestone. 
Serositis. 
Strictures common. 
Spontaneous fistulae. 
Transmural. 
Sarcoid like granulomas are present.
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14
Q

What are the extra-intestinal manifestations of IBD? (6)

A

Hepatic: fatty change, carcinoma.
Skeletal: polyarthritis, ankylosing spondylitis.
Oral ulcers, pyoderma gangrenosum, erythema nodosum.
Renal stones.
Anaemia, thrombo/leukocytosis.
Amyloid, vasculitis.

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15
Q

What are the risk factors for colorectal cancer in ulcerative colitis? (7)

A
Early age of onset.
Duration >10 years.
Total colitis.
Primary sclerosing cholangitis.
Family history.
Severe inflammation.
Dysplasia presence.
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16
Q

Name the non-neoplastic polyps of the colo-rectum. (6)

A
Hyperplastic.
Hamartomatous (Peutz-jeghers, juvenile).
Mucosal prolapse related.
Post inflammatory.
Inflammatory fibroid.
Benign lymphoid.
17
Q

Describe the pathology of hyper plastic polyps.

Size, location, ca risk.

A

1-5mm. Common. Often multiple.
In rectum and sigmoid colon.
Small and distal: NO Ca potential.
Large right sided may give rise to miscrosatellite unstable carcinoma.

18
Q

Describe the pathology of juvenile polyps.

Shape, size, who, ca potential.

A

Often pedunculate. 10-30mm.
Common in children.
Sporadic: NO Ca potential.
Juvenile polyposis increased colorectal + gastric Ca risk.

19
Q

What is peutz-jeghers syndrome?

Gene, symptoms (3), external feature

A

Autosomal dominant - STK11 gene. Increased Ca risk.
Teens - abdo pain, GI bleeds + anaemia. Multiple GI polyps - mostly small bowl.
Also muco-cutaneous pigmentation.

20
Q

What are adenomas in the colon?

Risks, distribution.

A

Benign epithelial tumours.
Polypoid.
Precursor to 80% of CRC. Adenocarcinoma sequence over 10-15 years.
Evenly distributed, larger in recto-sigmoid + caecum.

21
Q

What are the risk factors for colonic adenomas becoming malignant? (5)

A
Flat.
Size >10mm.
Villous + Tubule-Villous.
Severe displasia.
HNPCC associated adenomas.
22
Q

What are the risk factors for colorectal cancer? (9)

A
Diet. Obesity. Alcohol.
NSAIDs, HRT, OC.
Schistosomiasis.
Radiation.
IBD.
23
Q

Describe the genetics of Familial adenomatous polyposis (FAP).
Inheritance, risk, mutation.

A

Autosomal dominant.
100% risk of large bowel cancer.
Mutation in APC tumour supressor gene.

24
Q

Describe the genetics of HNPCC.

Inheritance, risk, mutation.

A

Autosomal dominant.
50-70% risk large bowel cancer, increased risk of others.
Mutation in DNA mismatch repair genes.

25
Q

How does colorectal cancer spread? (5)

A
Direct invasion.
Lymph metastasis.
Haematogenous mets (liver + lung).
Transcoelemic mets.
Iatrogenic.
26
Q

What is the Dukes staging used for and what are the stages?

5 year survival?

A
Colorectal cancer.
A: confined to bowel wall >90%.
B: invades bowel wall 70%.
C: regional lymph node mets. 40%
D: distant mets