Colorectal Cancer Flashcards

1
Q

What are the differentials for fresh blood in the stool?

A
  • Haemorrhoids
  • Acute anal fissure (following trauma or severe constipation)
  • Colo-rectal neoplasms
  • Acute proctitis
  • IBD
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2
Q

How do you differentiate between haemorrhoids and anal fissures?

A

Anal fissures present with severe pain on defecation

Haemorrhoids do not have pain but bright red blood is separate from the stool

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3
Q

What is an anal fissure?

A

Break/tear in the skin of the anal canal caused by over-stretching of the anal mucosa

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4
Q

Where do colorectal malignancies most commonly occur?

A

2/3 within colon
- Mostly in the left half (recto-sigmoid colon)
- Second most common = caecum
1/3 within rectum

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5
Q

What are the clinical features of colorectal cancer?

A
  • Sudden change in bowel habit
  • Unexplained microcytic anaemia (iron deficiency)
  • Abdominal/rectal mass
  • Intestinal obstruction
  • Abdominal pain
  • Tenesmus
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6
Q

What are the red flags of colorectal cancer?

A
  • Family Hx
  • Change in bowel habit >60yrs
  • Anaemia
  • Unexplained weight loss
  • Rectal bleeding
  • Rectal or abdominal mass
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7
Q

What are the risk factors for colorectal cancer?

A
  • Increasing age
  • Adenomatous polyposis coli (APC) mutation (FAP)
  • Lynch syndrome (HNPCC)
  • MYH-associated polyposis
  • Hamatomatous polyposis syndromes
  • IBD
  • Obesity
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8
Q

When would you send patients down the 2WW pathway?

A
  • > 40 with unexplained weight loss and abdominal pain
  • > 50 with unexplained rectal bleeding
  • > 60 iron-deficiency anaemia or changes in bowel habit
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9
Q

How do you diagnose colorectal cancer?

A
  • Barium enema or Colonoscopy
  • CT colonography
  • PET
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10
Q

What is CEA (carcinoembryonic antigen) used for?

A

Predicts and detects recurrence of colorectal cancer

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11
Q

Who is screened for colorectal cancer and how often?

A

• Aged 60-74, 2-yearly

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12
Q

If the faecal occult blood test is +ve, what is done next?

A

Colonoscopy

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13
Q

What are the inherited CRCs with polyposis?

A
  • Familial Adenomatous Polyposis (FAP)
  • Peutz Jeghers Syndrome (PJS)
  • Juvenile Polyposis Syndrome (JPS)
  • MUTYH Associated Polyposis (MAP)
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14
Q

What is the inherited CRC without polyposis?

A

Hereditary Non-Polyposis Colorectal Cancer (HNPCC) /Lynch syndrome

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15
Q

What is Familial Adenomatous Polyposis (FAP)?

A
  • Autosomal dominant mutation in the APC tumour suppressor gene
  • Causes multiple colorectal adenomas which undergo malignant transformation
  • CRC in 20-30s
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16
Q

What is K-ras?

A
  • Oncogene (gain of function)
17
Q

What is P53?

A
  • Tumour suppressor gene (loss of function)
18
Q

What is MUTYH Associated Polyposis (MAP)?

A
  • Autosomal recessive mutation in MUTYH

- Proximal colon cancer

19
Q

What is Peutz Jeghers Syndrome (PJS)?

A
  • Autosomal dominant mutation in STK11
  • Multiple hamartomatous polyps in the small intestine and colon
  • Melanin pigmentation of the lips, mouth and digits
20
Q

What is Juvenile Polyposis Syndrome (JPS)

A
  • Autosomal dominant mutation in SMAD4

- Mucus-filled hamartomatous polyps are found in the colorectum

21
Q

What is Hereditary Nonpolyposis Colorectal Cancer (HNPCC) / Lynch Syndrome?

A
  • Autosomal dominant mutation in mismatch repair (MMR) genes
  • More likely to be right-sided
  • Onset 30-50s
22
Q

What other cancers does Hereditary Nonpolyposis Colorectal Cancer (HNPCC) / Lynch Syndrome make patients at higher risk of developing?

A
  • Endometrial cancer (most common)
  • Ovary
  • Stomach
  • Small intestine
  • Hepatobiliary tract
  • Urinary tract
23
Q

What is the preventative treatment for HNPCC/ Lynch syndrome?

A

Aspirin 150-300mg o.d.