colorectal CA Flashcards

1
Q

DDx of BRBPR (4)

A
  • hemmoroids
    2. proctiis (IBD)
    3. polyps
    4. CA
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2
Q

*** what is important about hemmooids

A

diagnosis of exclusion - need to rule out all others

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3
Q

what is important in workup of anemia

A

scope

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4
Q

what is only way to say lesion is not malig.

A

look under a microscpe

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5
Q

what is part of blood supply to colon that systemic

A

middle and inferior rectal

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6
Q

epi

A

3rd most common CA

  • 12% of all CA in ont.
  • male>female
  • 1/3 local, 1/3 regional, 1/4 mets
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7
Q

sporadic causes (majority

A
  • AGE
  • men
  • env. (diet, obese, DM)
  • personal Hx of CRC or polyps
  • fam. Hx
  • IBD
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8
Q

3 known hereditary

A
  1. HNPCC
  2. FAP
  3. MYH polyposis
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9
Q

what is precursor to CA

A

adenoma that can then be removed- target for screenign

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10
Q

what is tubular adenoma

A

adenomatous epi with a stalk

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11
Q

what is villous adenoma

A

sessile ( no stalk) with finger-like projections

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12
Q

2 features of high grade dysplasia

A
  1. nuclear atypia

2. architectural complexity

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13
Q

WHO definition

A

metastitis (carcinoma def.) of the colon and rectum requires invasion of the muscilaris mucosa into the submucosa

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14
Q

3 variants

A
  1. mucinous - > 50% of lesion has extracellula mucin epithelium
  2. signet ring cell - > 50% with prominent intracytoplasmic mucin
  3. other rare types
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15
Q

2 grade types

A

low - 50-100% gland formation

high - 0-49% gland formation

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16
Q

3 margins

A
  1. proximal
    2 distal
  2. radial - around fatty edge
17
Q

what is problematic margins

A

1mm is same as being at the edge

18
Q

2 types of polyps

A

neoplastic and non

19
Q

3 non-neoplastics

A
  1. hyperplastic
  2. inflammatory
  3. juvenile
20
Q

3 neoplastic

A
  1. adenomatous - all dysplastic
  2. serrated
  3. hamarotomatous
21
Q

3 types of adenomatous polyps

A
  1. pedunclulated
  2. sessile or tubular
  3. villous
22
Q

epi of adenomatous polyps

A

v. common
- 1/4 will become CA
- need to be removed

23
Q

what is FAP

A

1-2% of patients with CRC

  • develop in teens
  • carpet of polyps
  • APC gene mutation
  • ALL NEED prophylactic colectomy
24
Q

what is attenuarted FAP

A
  • later age
  • less polyps
  • may spare rectum
  • same APC, but point mutation
25
Q

what is HNPCC

A
3% of all CRC
- other associated CAs
3,2,1 rule - 3 relatives, 2 gens, 1 first degree
- mismatch repair gene mutation
- 80% risk of CRC
26
Q

screening for avg.

A
  • no family Hx, or over 60
    @ 50, scope q10 years
    annual FOBT
27
Q

screening for moderate risk

A

fam Hx, or 1st degree relative

28
Q

screening for FAP

A

scope annually in teens until surg

29
Q

screen for HNPCC

A

scope biannually from 20-25 and annually from 40 onward

30
Q

screen for IBD

A

scope q 1-2 years after 8 years of colitis

31
Q

5 common presentations of CRC

A
  1. BRBPR
  2. change in bower habits
  3. abdo pain or mass
  4. weight loss
  5. anemia
32
Q

diagnosis

A

scope with biopsy

33
Q

***best predictor of survival

A

nodal status

34
Q

what is treatment

A

curable - surg with 5cm margins
node + - adjuvant chemo
incurable - chemo

35
Q

what is treatment for incurable

A

chemo and pallaitice surgery or stents

36
Q

what is done for survors

A
  • followed 5-10 years
  • scopes q 1,3,5 years
  • CEA q 6 months