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
what is HNPCC
``` 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
screening for avg.
- no family Hx, or over 60 @ 50, scope q10 years annual FOBT
27
screening for moderate risk
fam Hx, or 1st degree relative
28
screening for FAP
scope annually in teens until surg
29
screen for HNPCC
scope biannually from 20-25 and annually from 40 onward
30
screen for IBD
scope q 1-2 years after 8 years of colitis
31
5 common presentations of CRC
1. BRBPR 2. change in bower habits 3. abdo pain or mass 4. weight loss 5. anemia
32
diagnosis
scope with biopsy
33
***best predictor of survival
nodal status
34
what is treatment
curable - surg with 5cm margins node + - adjuvant chemo incurable - chemo
35
what is treatment for incurable
chemo and pallaitice surgery or stents
36
what is done for survors
- followed 5-10 years - scopes q 1,3,5 years - CEA q 6 months