Pathology of Colorectal Cancer Flashcards

1
Q

Give an overview of the epidemiology of colorectal cancer.

A
  • 3rd most common cancer diagnosed worldwide.
  • Incidence and mortality are 25% lower in women than men.
  • Highest rates in developed countries - can be considered a ‘Western disease’.
  • Decreased in developed countries due to nationwide screening programmes, improved surgery and uptake of colonoscopies.
  • However, an increased trend in <50s has been observed - potentially due to lifestyle, obesity and environmental factors.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the risk factors for colorectal cancer?

A
  • Non-modifiable
    • Age
    • Sex
    • IBD
    • FHx
  • Modifiable
    • Diet (low fibre and high fat)
    • Lack of exercise
    • Smoking
    • Alcohol
    • Obestiy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Describe the clinical presentation of coloretal cancer.

A
  • Early stage CRC is usually asymptomatic until more advanced stages.
  • Therefore screening plays a major role in diagnsing curable (early stage) disease or precursors to disease.
  • Symptoms:
    • Occult or overt rectal bleeding
    • Change in bowel habit (diarrhoea or constipation)
    • Pain & discomfort in bowel
    • Weakness and fatigue
    • Weight loss
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How is colorectal cancer diagnosed?

A
  • Rectal bleeding and discomfort in bowel and change in bowel habit may not be due to cancer. Bleeding is a common symptom of both benign and malignant causes.
  • Endoscopy
    • Colonoscopy is the most common, but invasive, method to diagnose colorectal cancer.
  • Imaging
    • CT colonography is used as a complementary imaging method for the diagnosis of polyps and colorectal cancer.
    • Also used for assessing the stage of the disease both locally (colon) and distant (e.g. lesions in the liver).
  • Labooratory
    • Complete blood count, as checking CEA concentrations at the time of diagnosis (high CEA = worse prognosis).
  • Pathology
    • Histological assessment is the basis for pathological diagnosis and staging of the disease.
    • Mismatch repair testing (immunohistochemistry) is used for diagnosis of lynch syndrome and adjuvant immunotherapy decision making.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Name and describe each layer of the colon.

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Which features of the colon are depicted in these histological sections?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Name each of these features of colon cancer histopathology shown in this slide.

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Name each of these features of colon cancer histopathology shown in this slide.

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the factors which affect prognosis for colorectal cancer?

A
  • The earlier the detection, the better the prognosis.
  • Generally:
    • 1 year survival 80%
    • 5 year survival 60%
  • What affects prognosis and survival?
    • TNM staging
    • Other histopathological features
    • Health and fitness
    • Effectiveness of surgery and treatment
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Describe the ‘T’ staging of colorectal cancer.

A
  • T = extent of local invasion.
  • pT0 = no evidence of primary tumour.
  • pT1 = tumour invades submucosa.
  • pT2 = tumour invades muscularis propria.
  • pT3 = tumour invades into subserosa or into perirectal tissues.
  • pT4 = tumour perforates visceral peritoneum (4a) and/or directly invades other organs or structures (4b).
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Describe the ‘N’ staging of colorectal cancer.

A
  • pN = extent of regional lymph node invasion.
  • pN0 = no positive regional lymph nodes.
  • pN1 = 1-3 regional lymph nodes involved.
    • pN1a = metastasis in 1 regional lymph node
    • pN1b = metastases in 2-3 regional lymph nodes
    • pN1c = tumour deposit
  • pN2 = metastatic disease in 4 or more regional lymph nodes.
    • pN2a = metastases in 4-6 regional lymph nodes.
    • pN2b = metastases in 7 or more regional lymph nodes.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe the ‘M’ staging of colorectal cancer.

A
  • M = extent of distant metastasis.
  • pM1a = metastasis confined to one organ without peritoneal metastases.
  • pM1b = metastases in more than 1 organ.
  • pM1c = metastases to the peritoneum with or without other organ involvement.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the prognosis for a patient who has colorectal cancer?

A
  • 5 year survival:
    • 95% of men and ~100% of women survive stage 1 CRC.
    • 80% of men and ~90% of women survive stage 2 CRC.
    • 65% of men and women survive stage 3 CRC.
    • 25-40% of patients survive stage 4 CRC if the tumour can be surgically removed from the liver.
    • 5% of men and 10% of women survive stage 4 CRC.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the other prognostic factors for a patient with CRC (other than TNM)?

A
  • Differentiation (grade) - architecture and specifically gland formation (how closely it resembles a normal gland).
  • Tumour deposits - discrete nodules of cancer in the tissue’s lymph drainage area, separate from the primary tumour and with no lymph node or identifiable vascular or neural structures.
  • Venous invasion - has it invaded the blood vasculature.
  • Lymphatic invasion - has it invaded the lymphatic vessels.
  • Perineural invasion - has it invaded the space surrounding a nerve.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe the pathogenesis of colorectal cancer.

A
  • Most CRCs arise from a polyp.
  • Progression from a polyp (precursor lesion) to cancer can take 10-15 years.
  • Cell of origin is thought to be a stem cell in the base of the colonic crypts.
  • Progression is a result from multiple genetic mutations and epigenetic alterations.
  • 2 major pathways to neoplastic disease
    • Adenoma to carcinoma sequence (chromosomal instability).
    • Serrated neoplasia sequence (microsatellite stable or instable).
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the variants of CRC?

A
  • Adenocarcinoma (70-90%)
  • Serrated neoplasia (10-20%)
  • In 95% of cases, these are sporadic cancers.
  • 5-7% hereditary (Lynch syndrome and FAP).
  • Rare variants:
    • Mucinous adenocarcinoma
    • Signet ring-cell carcinoma
    • Neuroendocrine
17
Q

Why is it important to know the different molecular subtypes of CRC?

A
  • There are different molecular subtypes which occur in different areas of the colon.
  • The reason for molecular subtyping is because it affects the efficacy of different treatments.
  • Prognostic and treatment decisions can be made on molecular subtyping and not just histopathological staging and features.
18
Q

What are the prevention strategies for CRC?

A
  • Stop smoking
  • Eat healthily
  • Exercise
  • Drink alcohol within recommended limits
  • Maintain a healthy weight
  • Aspirin