Colorectal Cancer, Merter Flashcards

1
Q

What are the symptoms of colorectal cancer/

A

BAP, SSAID
Bleeding
Anorectal pain
Pelvic pain/Pain
,
Swelling
Stomach ache
Anal discharge
Incontinence
Defecation change=constipation/dirrhea

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2
Q

In which side of the colon is the perforation more likely to occur?

A

Left colon, bcz it is much smaller than the right

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3
Q

Obstruction in the right /left colon will lead to what?

A

*perforation

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4
Q

Having a tumor in which side of the colon will cause bleeding and Anemia

A

Right colon

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5
Q

Clinical evaluation of colorectal cancer?

A

Family history
CT
MRI
Colonoscopy
PET-CT

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6
Q

Colectomy:
Colostomy:

A

Colectomy: removal of colon/section of colon
Colostomy: forming a an exterior stoma for the colon to excrete the feces

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7
Q

Which type of polyp has 100% colorectal cancer risk?

A

FAP; familial adenomatous polyposis

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8
Q

Any polyp that is …….. has a high risk of being cancerous?

A

Adenomatous

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9
Q

What are the etiologies of CRC?

A

-Age 40-50>
-Gender;25% more in males
-Having the APC gene affected by FAP disease
-BRCA gene mutation
-5% Hereditary CRC’s
-80% HNPCC (hereditary nonpolyposis CRC)
-Having Crohn’s or ulcerative colitis

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10
Q

In which patients does the risk of CRC increases 3.5-6.5 times?

A

1)adenomatous* polyp larger than 1cm*
2)villous or tubulovillose polyp
3)high grade dysplasia*

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11
Q

What are other etiological factors for CRC?

A

-Acromegaly
-Diabetes milletus
-obesity
-insulin resistance

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12
Q

What are the lifestyle risks that inc the chances of having CRC?

A

-Red/processed meat
-smoking
-alcohol
-androgen therapy (fertility-related )

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13
Q

Which type of polyp provides a risk for CRC?

A

Neoplastic (adenomatous) polyps has high risk for cancer dev.

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14
Q

Which type of the Neoplastic (adenomatous) polyps has the highest risk of CRC?

A

1-Villous adenoma type 40%

(2-tubular adenoma5% & 3-Tubulovillous adenoma 22%)

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15
Q

What are the polyp size classifications according to their level of risk for cancer?

A

<1cm=<1% ca
1cm=10%risk ca
2cm=15% risk ca

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16
Q

Describe the treatment for each cancer case?

1-In-situ cancer:
2-Invasive ca; in-pedunculated polyp :
3-Invasive ca; sessile polyp:

A

1-polypectomy(removal of polyps in the colon)
2-polypectomy
3-colon resection

17
Q

APC gene mutation is positive in which diseases related to CRC?

A

FAP (familial adenomatous polyposis) ;APC 75% +ve
&
Attenuated form of FAP; APC 60% +ve and needs screening at the age of 15 plus colonoscopy

18
Q

What is the Amsterdam criteria for HNPCC (hereditary non-polyposis colorectal cancer)/Lynch Syndrome diagnosis?

A

-3 relatives with colorectal cancer, where one of them is 1st degree.
- 2 generations of colorectal cancer
- 1 colorectal cancer before age of 50
- FAP is excluded

19
Q

What is the pathway of carcinoma development in Lynch syndrom (HNPCC)?

A

RER pathway, DNA mismatch repair gene defect (hMLH1, hMSH2)

20
Q

What is the pathway of carcinoma development in FAP?

A

APC gene mutation

21
Q

What are the Bethesda criteria?

A

1-Amsterdam criteria is met

2- 2 or more HNPCC related malignancies in one patient.

3-1st degree relative with CRC or HNPCC; one of the cancers diagnosed <45 yr

4-colon or endometrial ca diagnosed <45 yrs

5-diagnosed w/ adenoma before the age of 40

6-signet ring cell or undifferentiated right colon ca <45 yrs

22
Q

What is the most imp sign for poor prognosis in CRC?

A

Lymph node metastasis (BY TNM staging)

23
Q

Know TNM staging for malignant metastasis;

A

Tis; tm in mucosa
T1; tm in submucosa
T2;tm in muscularis propria
T3; tm in serosa
T4; tm spread into visceral peritoneum

N1;1-3 lymph node in pericolic and perirectal involved
N2; 4> LN pericolic or perirectal involved
N3; vascular pedicle(cardiac) LN involvement

M0;no metastasis
M1; metastasis

24
Q

what is a specific finding in FAP?

A

retinal pigment epithelial hypertrophy

25
Q

describe stage 1 CRC

A

T1-2,N0,M0

26
Q

describe stage 2 CRC

A

T3-4,N0,M0

27
Q

describe stage 3 CRC

A

Tany,N1-3,M0

28
Q

describe stage 4 CRC

A

Tany,Nany,M1

29
Q

what is the surgical treatment for FAP?

A

restorative proctocolectomy (procto=rectum), J-pouch ileoanal anastomosis

30
Q

what are the diagnostic tests required for FAP?

A

colonoscopy and endoscopy (since periampullary tumors and GIS polyps dev)

31
Q

which disease is characterized by being autosomal dom with Hyperpigmentation and hamartomatous(benign) polyps found in the small intestines plus in the rectum and colon

A

peutz -jegher syndrome

32
Q

describe the 3 types of polyps and which surgery they require ?

A

sessile polyp; colon resection
in situ ca; polypectomy
in-pedunculated ; polypectomy

33
Q

which disease is symptomatic at 16yrs with many adenomatous polyps which if left untreated before 45yrs, 90% can dev into CRC and lifetime risk of 100%

A

FAP

34
Q

which CRC risky diseases occur in children b/w 10-12 yrs

A

FAP

35
Q

which CRC risky diseases occur in patients b/w 20-25 yrs

A

HNPCC

36
Q

which diagnostic staging method is used to diagnose CRC?

A

TNM staging