Colon polys and Cancer Flashcards

1
Q

Proximal colon

A

ascending and transverse colon

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2
Q

What are the 4 parts of the colon

A
  • ascending
  • transverse
  • descending
  • sigmoid
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3
Q

What vitamin does the colon absorb

A

vitamin K

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4
Q

What is a polyp

A

growth in the inner lining of the colon

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5
Q

How are polyps diagnosed

A
  • colonoscopy
  • barium enema
  • sigmoidoscopy
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6
Q

Physical exams signs common with polyps

A

usually asymptomatic

can have GI bleed or intestinal obstruction

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7
Q

Symptoms of polyps

A
  • BRBPR
  • rectal tenesmus
  • change in bowel habits
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8
Q

What are the 4 morphologic characteristic of polyps

A
  • sessile
  • flat
  • pedunculated (polypoid)
  • depressed
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9
Q

Which two shapes of polyps are associated with malignancy

A

flat and depressed

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10
Q

Classifications of non- neoplastic polyps

A
  • mucosal
  • inflammatory pseudopolyps
  • hyperplastic
  • submucosal
  • hamartamous
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11
Q

Classification of neoplastic polyps

A

adenomatous polyps

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12
Q

What are muscoal polyps

A

small polyps that resemble adjacent tissue and are histologically normal

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13
Q

What are inflammatory pseudopolyps?

A

irregularly shaped islands of intact mucosal

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14
Q

What causes inflammatory pseudopolyps

A

mucosal ulceration and regeneration (inflammatory bowel disease process)

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15
Q

What are the most common non-neoplastic polyps

A

hyperplastic

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16
Q

What pattern do hyperplastic polyps present with

A

serrated or sawtooth pattern

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17
Q

Where are most hyperplastic polys found?

A

rectosigmoid

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18
Q

What are the types of submucosal polyps

A
  • lymphoid
  • fibromas
  • lipoma (most common)
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19
Q

Why do hyperplastic polyps have to be removed

A

they are impossible to distinguish from adenomatous polys so they need to be biopsied

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20
Q

Which type of polyps do most polyposis syndromes derive from

A

hamartamous polyps

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21
Q

How long does it take adenomatous polyps to develop into cancer? What type of cancer?

A

7-10 years

adenocarcinoma

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22
Q

What are some risk factors for adenomatous polyps

A
  • older age
  • increased BMI
  • lack of physical activity
  • smoking
  • men>women
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23
Q

What are the histological classifications of adenomatous polpys

A
  • tubular
  • tubulovillous
  • villous
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24
Q

Which type of adenomatous polyp has the highest malignancy potential

A

villous

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25
Q

Which type of adenomatous polyp is most common

A

tubular

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26
Q

What characteristics of adenomatous polyps are associated with high CRC risk

A
  • villous histology
  • high grade dysplasia
  • number and size (one or more greater than 1 cm or more than 3 of any size)
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27
Q

Screening/diagnostic tests for polyps

A
  • FOBT
  • double contrast barium enema
  • CT colonography
  • flex sig
  • colonoscopy
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28
Q

What does an FOBT look for

A

blood in the stool–> bleeding polyp

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29
Q

What would a double contrast enema show if there were polyps

A

applecore narrowing of the colon with distension

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30
Q

What is the gold standard for examining polyps? What major benefit does it have?

A

colonoscopy

can remove the polyps immediately

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31
Q

What are the risk associated with colonoscopy

A
  • perforation
  • bleeding
  • intolerance to sedation
  • dehydration/electrolyte imbalance in elderly
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32
Q

What is a polypectomy

A

removal of polpys

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33
Q

What technique is used to remove a <5mm diminutive polyp

A

cold biopsy forceps or cold snare excision

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34
Q

What technique is used to remove a 5-10 cm polyp

A

standard snare excision

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35
Q

What technique is used to remove large sessile polyps (2-3cm)

A

piecemeal excision
or
saline assisted endoscopic mucosal resection

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36
Q

When should you do a follow up colonoscopy if you removed a polyp >2cm or you are concerned for incomplete removal of polyps

A

3-6 months

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37
Q

If you find >10 adenomas, when should you do a follow up colonoscopy

A

in less than 3 years

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38
Q

For most polyps found on endoscopy, when should a follow up colonoscopy be done?

A

3 years

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39
Q

If small tubular adenomas <10mm or sessile serrated polyps with no dysplasia are found when should a follow up colonoscopy be done?

A

5 years

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40
Q

If there are no polyps found or small hyperplastic polyps <10mm are found when should a follow up colonoscopy be done?

A

10 years

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41
Q

When do you consider that your patient might have a hereditary intestinal polyposis syndrome

A
  • family history of CRC affecting more than one family member
  • personal of family hx of CRC >50
  • personal or family history of multiple polyps (>20)
  • personal or familiy hx of multiple extracolonic malignancies
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42
Q

Which is the most common inherited colon cancer

A

lynch syndrome

43
Q

What part of the colon does lynch syndrome typically affect? What kind of polyps does it cause?

A

right colon

adenomatous

44
Q

What is the most common extracolonic malignancy with lynch syndrome

A

endometrial carcinoma

45
Q

What is turcot syndrome

A

varient of extracolonic malignancy that affects the brain

46
Q

What are the cancers/masses tested for if lynch syndrome is suspected

A

microsatellite instability

47
Q

What is the treatment for lynch syndrome

48
Q

When are colonoscopies done in a patient with lynch syndrome

A

every 1-2 years starting at age 20-25

49
Q

How is familial adenomatous polyposis characterized

A

> 100 adenomas

50
Q

What other cancers does FAP increase a patients risk for

A
  • small bowel
  • gastric
  • pancreatic
  • thyroid
51
Q

What is Gardner syndrome

A

FAP patients with extracolonic manifestations

52
Q

What types of extracolonic manifestations do patients with FAP have

A
  • desmoid tumors
  • extra teeth or missing teeth
  • congenital hypertrophy of the retinal pigment
  • duodenal adenomas
  • fundic gland polyps
53
Q

What is the most common type of extracolonic manifestation in a patent with FAP

A

desmoid tumor

54
Q

When does screening begin in patients with FAP

A

10-12 start with yearly flex sigs

55
Q

How are patients with FAP treated

A
  • prophylactic colectomy
  • screen remaining rectum every 6 months- 2 years
  • EGD at 20 to 25 every 1 to 3 years
  • use NSADI and COX2 as chemoppx
56
Q

What types of hamartomatous syndromes

A
  • familial juvenile polyposis

- peutz jeghers polyposis

57
Q

Where does familial juvenile polyposis present

A
  • small bowel
  • stomach
  • colon
  • rectum
58
Q

What are the symptoms of familial juvenile polyposis

A

typically asymptomatic

can have

   - painless rectal bleeding
   - rectal prolapse
   - failure to thrive
59
Q

How are patients with familial juvenile polyposis screened

A

start at age 15 and every 1-3 years after

60
Q

What things give a diagnosis of familial juvenile polyposis

A
  • > 5 juvenile polys in the colon
  • multiple juvenile polys in the GI tract
  • family hx/genetic testing
61
Q

What is Peutz- Jehgers syndrome

A

inherited GI diorders where patients develop polyps on the mucous lining of the intestine and dark discolorations on the skin and mucous membrane

62
Q

How to patients with PJS present

A

GI bleeding, intussusceptions or obstructions

63
Q

What are the most common extracolonic malignancies associated with PJS

A

breast and testicular cancer

64
Q

What screening needs to be done in patients with PJS

A
  • colonscopy every 2-3 years at age 18
  • EGD every 2-3 years at age 10
  • breast and testicular exams
65
Q

How often should you do a colonscopy? flex sig? flex sig plus fit? CT colonography?

A

colonoscopy: 10 years

flex sig: 5 years

flex sig with FIT: 10 years

CT colonography: 5 years

66
Q

How often should you do cancer detection tests? What are they?

A

annually

  • fecal immunochemical test
  • fecal occult blood test
  • fecal DNA
67
Q

When should cancer prevention and cancer screening tests begin?

A

over 50

over 45 in African Americans

68
Q

When do patients stop getting screened for CRC

69
Q

When do you begin to screen patietns with a 1st degree relative w/ CRC <60 or two 1st degree relatives of any age? When do you repeat it?

A

40 or 10 years before family member was diagnosed

repeat every 5 years

70
Q

When do you screen a patient with a personal history of CRC

A

-total colon examination 1 year after resection
-repeat a 3 years
if normal repeat at 5

71
Q

When should you screen a patient with IBD?

A

8 years after onset of pancolitis, repeat every 1-2 years

72
Q

Most common location for colorectal cancer

A

left side (rectum, rectosigmoid)

73
Q

Where does colorectal cancer commonly metastasize to

A

lymph nodes, liver, lung, peritoneum

74
Q

What are some modifiable risk factors for colorectal cancer?

A
  • “western diet”
  • obesity
  • smoking
  • alcohol consumption
  • diabetes
75
Q

What are non modifiable risk factors for colorectal cancer?

A
  • being african american
  • heriditary polyposis syndromes
  • family hx
  • IBD
  • abdominal radiation in childhood
76
Q

Symptoms of right sided colon cancer

A
  • vague abdominal pain
  • iron deficiency anemia
  • fatigue/weakness
  • GI bleeding
77
Q

Symptoms of left sided colon cancer

A
  • obstructive sx
  • colicky abd pain
  • change in bowel habits
  • stool streaked with blood
78
Q

Symptoms of rectal cancer

A
  • rectal tenesmus
  • urgency
  • recurrent hematochezia
  • narrow caliber stools
79
Q

Physical exam findings of a patient with colon cancer

A
  • rectal bleeding

- abdominal pain

80
Q

What physical exam findings would indicate progressive colon cancer

A
  • cachexia/weightloss
  • back pain
  • urine or bowel changes
  • acites
  • pallor
81
Q

What tests do you need to get before you can stage colon cancer?

A
  • CBC with diff
  • LFTs
  • CEA level (tumor marker)
  • CT chest/abd/pelvis
  • endorectal ultrasound
82
Q

How many lymph nodes do you need to dissect to stage colon cancer

83
Q

What is the treatment for colorectal cancer

A
  • surgery: resection is treatment of choice
  • chemo (stages III or IV)
  • radiation plus chemo stages II-IV
84
Q

What are the surgical options for colon cancer?

A
  • laprascopic colectomy
  • open colectomy

+/- ostomy

85
Q

What are the surgical options for rectal cancer

A
  • total mesorectal excision
  • transanal excision
  • transanal endoscopic microsurgery
  • transsphincteric excision
  • low anteriorrescection with colorectal anastamosis
  • abdominoperineal rescection with a colostomy
86
Q

Treatment of stage I colon cancer

87
Q

Treatment of stage II colon cancer

A

colectomy

*adjuvent therapy typically not indicated

88
Q

Treatment of stage III colon cancer

A

colectomy + adjuvent therapy

CapeOx or 5-FU/leucovorin or folfox

89
Q

Treatment of stage IV colon cancer

A

chemotherapy

folfox or folfiri +/- biologic

+/- resection of lung or liver met
+/- colectomy

90
Q

How often is a physical exam done after surgery for colorectal cancer

A

every 3-6 months for two years then every 6 months for three years

91
Q

When is a abd/pelvic CT done after surgery for colorectal cancer?

A

anually for 5 years

EXCEPT if resceted metastasis
every 3-6 months for 2 years then every six months for 5 years

92
Q

When are colonoscopies done after surgery for colorectal cancer

A

1 year after surgery then every 3 years, can do every 5 years if negative

93
Q

When are proctoscopies done after surgery for rectal cancer

A

every 6 months for 3-5 years

94
Q

What is the most common type of anal cancer

A

small cell carcinoma

95
Q

Non keratinizing SCC of the anus

A

tumors arising above the dentate line of the anal canal

96
Q

Keratinizing SCC of the anus

A

tumors arising distal to the dentate line

97
Q

What are other types of anal cancer you can get?

A
  • adenocarcinoma
  • melanoma
  • sarcoma
98
Q

What is anal cancer caused by

99
Q

Risk factors for anal cancer

A
  • HPV
  • HIV
  • genital warts
  • smoking
  • receptive anal intercourse
  • chronic immunosuppressive conditions
100
Q

Initial tests for diagnosis of anal cancer

A
  • endoscopy with biopsy
  • anoscopy
  • rigid proctosigmoidoscopy
101
Q

Tests for workup of anal cancer

A
  • CT or MRI or abd/pelvis
  • PET scan
  • fine need aspiration or biopsy of node if noted on imaging
102
Q

Treatment of stage 0-III anal cancer

A

neoadjuvant chemotherpay and surgery

103
Q

Treatment of stage IV anal cancer

A
  • systemic chemotherapy

- palliative chemoradiotherapy

104
Q

What is the post treatment surveillance for a patient that had rectal cancer? How often is it done?

A
  • DRE
  • anoscopy
  • inguinal node palpation

every 3-6 months for 5 years

+/- CT annually for three years