Appendix and colon tumors Flashcards

1
Q

Appendix tumors are very ___ and are usually discovered accidently post ___.

A

rare

appendectomy

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2
Q

What is the most and second most common tumors in the appendix?

A

carcinoid

AC

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3
Q

The ___ of the appendix tumor is the best predictor to the level of its aggressiveness and malignancy

A

size

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4
Q

Appendix carcinoid tumor < 1 cm should be treated as a ___ tumor- treating with regular ___

A

benign

appendectomy

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5
Q

Appendix carcinoid tumor > 2 cm should be treated aggressively with ____ and regional ___

A

right hemicolectomy

lymphadenectomy

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6
Q

Appendix AC should be treated like AC of the cecum with- ____ and regional ___. We can also use adjuvant treatment of ____

A

right hemicolectomy
lymphadenectomy
FOLFOX (5 fu, leucovorin, oxaliplatin)

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7
Q

When finding cyst in the appendix, we should consider ___ tumor. Beware of leakage to prevent ___

A

mucinous

seeding

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8
Q

Colon polyps frequency increase with ___

A

age

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9
Q

__% of the polyps are found in the ___

A

50

rectum-sigmoid

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10
Q

Most colon polyps are ____, but may cause rectal ___ and ___

A

asymptomatic
bleeding
constipation

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11
Q

How can we characterize polyps as ___ or ___

A

non-neoplastic

neoplastic

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12
Q

Non-neoplastic polyps can be: (3)

A

inflammatory
hamartomatous
hyperplastic

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13
Q

Neoplastic polyps can be: (2)

A

adenomas

adenocarcinoma

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14
Q

2/3 of all polyps in the colon are of ___ type

A

adenoma

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15
Q

Inflammatory polyps develop in the ___ are called solitary ___ ___ syndrome and may lead to damage to the ___ sphincter, long lasting ___ leading to ___

A
rectum
rectal
ulcer
anorectal
constipation
ulceration
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16
Q

Juvenile tumors are ___, usually found in the ___ and characterized with rectal ___, usually in children < age of ___

A

pedunculated
rectum
bleeding
5

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17
Q

Peutz- Jeghers syndrome is __ with large ___ polyps scattered all around the GI. It leads to increased risk for different cancers

A

AD

pedunculated

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18
Q

Cronkhite–Canada syndrome ____tumors all along the GI with cutaneous ___, alopecia, nail ___, and ___ atrophy. This has no genetic disorder and not malignancy potential.

A

hamartomatous
hyperpigmentation
atrophy
tonsils

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19
Q

Name the 3 hamartomatous polyps

A

juvenile polyps
Peutz- Jeghers syndrome
Cronkhite–Canada syndrome

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20
Q

What are the most common non neoplastic polyps?

A

Hyperplastic

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21
Q

Hyperplastic polyps are usually found at the ages of __-__. It is an epithelial hyperplasia with ___ malignancy potential. Their hallmark is ___, usually located on the __ colon.

A

50-60
no
serrated
left (recto sigma)

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22
Q

Adenomatous polyps has ___ characteristics with risk to convert into ___

A

dysplastic

CRC

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23
Q

What are the macroscopic strictures of polyps? (2)

A

sessile :(

pedunculated :)

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24
Q

What kind of histological types adenomas can present with?
___ (65-80%)
___ (5-10%)
___ (10-25%)

A

Tubular (peduncular)
villous (sessile)
mixed

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25
Q

When performing pathology to the polyp, we need > __% to determine the type. If < ___% then mixed

A

80

60

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26
Q

The ___ the adenoma, the ___ likely it will progress to malignancy

A

bigger

more

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27
Q

Advanced (invasive) adenoma is defined by high grade ___ / > __cm / ___

A

dysplasia
1
villous

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28
Q

Treating all polyps includes ___ using ___ when performing ___

A

resection
snare
colonoscopy

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29
Q

Safe removal of polyp requires __ mm of clean margins

A

2

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30
Q

Invasive adenocarcinoma penetrates through the MM (___) and can ___

A

muscularis mucosa

metastasize

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31
Q

Non-invasive adenocarcinoma = carcinoma _____

A

in situ

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32
Q

Which classification is used for cancerous polyps?

A

Haggitt

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33
Q

Every sessile polyp with invasive carcinoma is considered level __

A

4

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34
Q

Pedunculated polyps levels - should be removed.

Every polyp level __ should be considered as CRC

A

3-4

4

35
Q
Give 10 risk factors to CRC:
old \_\_\_
Westman \_\_\_
personal \_\_\_
family history (remember syndromes (3))
IBD (2)
strep bovis bacteremia
radiation
obesity
smoking
A
age
diet
history
FAP/HNPCC/MYH
UC/CD
36
Q

Name 4 protective factors from CRC:

A

aspirin
estrogen
calcium/folic acid
low BMI

37
Q

What is the relevant marker for CRC?

A

CEA (Carcinoembryonic antigen)

38
Q

FAP is an ___ disease due to a mutation in the __ gene on chromosome __

A

AD
APC
5

39
Q

We must find at least ___ polyps to diagnose FAP. The mean age at diagnosis is __

A

100

29

40
Q

Although FAP adenomas do not have higher malignancy potential than sporadic adenomas, ___% of untreated patients will develop cancer, usually by the age of ___

A

100

30

41
Q

What is the preferred treatment for FAP

A

total proctocolectomy with ileoanal pouch

42
Q

FAP can also appear in the ___ or ___, therefor EGD (___) should be performed every __ years

A

Esophagogastroduodenoscopy

2

43
Q

Patients with FAP are recommended to go through surgery by the age of

A

20

44
Q

Describe the screening in FAP patients:

A
yearly colonoscopy starting at the age of 10-12
EGD every 2 years from the age of 30
thyroid every year
abdominal US (pancreas cancer)
yearly physical examination
45
Q

HNPCC= ____ and __

A

hereditary non polyposis colon cancer

lynch

46
Q

HNPCC may lead mostly to __ and ___, but also (3)

A
CRC
endometrium
stomach
ovary 
small bowel
47
Q

HNPCC is more common in the ___ colon, and at younger (__) age

A

right

46

48
Q

What are the common mutations in Lynch syndrome? (2)

A

MLH1

MSH2

49
Q

Describe the Amsterdam classification for Lynch (5)

A

CRC in 3 family members (at least 1 first degree)
2 generations involved
at least 1 of the mentioned above <50 when diagnosed
FAP ruled out
pathology

50
Q

How do you treat Lynch?

A

abdominal colectomy + ileorectal anastomosis

hysterectomy +BSO

51
Q

Who has better CRC prognosis? HNPCC or regular patient?

A

HNPCC, why? unclear…

52
Q

Describe the recommended screening for Lynch patient: (3)

A

colonoscopy every 2 years age 20-40 + every year when >40 or 10 years before the age the family member was diagnosed

pelvic examination (US) every 1-2 years from ages 25-35

renal/urinary US every 1-2 years ages 30-35

53
Q

Sporadic CRC adenocarcinoma is the ____ common GI tract malignancy

A

most

54
Q

The leading way CRC spreads is through the ___ to the regional ___ ___. If ___ than we will find tumors in the ___

A

lymph system
lymph nodes
hematogenic
liver

55
Q

____ has a protective effect from CRC through COX-2 inhibition

A

aspirin

56
Q

Name the common late symptoms for CRC: (7)

A
constipation
hematochezia 
iron deficiency anemia
abdominal pain
tenesmus
bowel obstruction
fistulas
57
Q

Left colon tumors tend to be more ___

A

obstructive

58
Q

Sigma tumors may imitate ___- (3)

A

LLQ pain
fever
leukocytosis

59
Q

Right colon tumors usually ____ and cause ___ and ___

A

bleed
iron deficiency
lethargy

60
Q

The gold standard for CRC is ____

A

colonoscopy

61
Q

Colon with complete obstruction due to tumor should be treated with ___ ___

A

urgent

surgery

62
Q

Why we should not perform primary anastomosis in urgent surgery due to complete bowel obstruction due to tumor?

A

lack of preparation which will lead to anastomotic leak

63
Q

Hartman procedure:

A

sigmoidectomy + end colostomy + rectal stump

64
Q

When dealing with a patient with a partial obstruction due to a tumor there is no indication for an ___ ___, ___ imaging, ___ functions, ___ levels, full ___, CT and MRI

A

urgent surgery
CXR
liver
colonoscopy

65
Q

Preoperative colon preparation includes: 1) mechanical (___), 2) ABx (PO (__,__,__)

A

PEG (laxative)

neomycin, erythromycin, Flagel

66
Q

When removing CRC we should strive for clean margin of ___ cm + ___ + ___

A

5
lymph nodes
mesentery

67
Q

Right hemicolectomy surgery requires the dissection of the ___ branches (3) and the right branch of the middle colic.

A

SMA
ilio-colic
middle colic
right colic

68
Q

Left hemicolectomy surgery requires the dissection of the left ___ artery + left branch of mid ___

A

colic

colic

69
Q
Staging of CRC:
1- \_\_\_
2- \_\_\_
3- \_\_\_
4- \_\_\_
A

T1/2 + N0 + M0
T3/4 + N0 + M0
any T + N1/2 + M0
any T + any N + M1

70
Q
What are the 5 years survival of CRC?
1- \_\_\_%
2- \_\_\_%
3- \_\_\_%
4- \_\_\_%
A

90
75
50
<5

71
Q

Treating stage 1 colon cancer is with ___ alone, ___ after 1 year. If no polyp, next colonoscopy after ___ years, if we find polyps- after 1 year. ___ levels should be monitored every ___ months in the first 2 years. If increased- CT/MRI/PET

A
surgery
colonoscopy
5
CEA
3
72
Q

Treating stage 2 colon cancer is with ___ + consider adjuvant chemotherapy (___) only in very severe patients. Monitor like in stage 1, but add CEA for 5 years every 6 months, and chest/abdomen CT once a year for ___ years

A

surgery
FOLFOX
3

73
Q

Name the 4 criteria for very severe colon cancer patient:

A

less than 12 nodes were resected
T4 tumor
poorly differentiated tumor
perforation

74
Q

Treating stage 3 colon cancer is with ___ and ___ for all patients. monitor like stage 2. ___ chemotherapy with FOLFOX4 (___)

A

surgery
chemotherapy
adjuvant
5fu+oxaliplatin+leucovorin

75
Q

Treating stage 4 colon cancer involves __ + __ + __

A

chemotherapy
biological
palliative surgery

76
Q

What does the stage 4 biological treatment include? (3)

A

Avastin (anti VEGF)
Erbitux
Panitumumab (anti EGFR)

77
Q

The best prevention test for CRC is ___ every __ years over the age of ___

A

colonoscopy
10
50

78
Q

For patients refusing colonoscopy- flexible ___/ coronographic __ every 5 years

A

sigmoidoscopy

CT

79
Q

If patients prefer to avoid all prevention tests- we move to ___ tests: (3)

A

detection
FIT- fecal immunochemical test
FOBT- fecal Occult Blood Test
Fecal DNA testing

80
Q

When performing colonoscopy and finding >__small adenoma + __ grade -> repeat colonoscopy within the next - years

A

1
low
5-10

81
Q
What is an advanced adenoma?
> \_\_cm
\_\_\_
\_\_\_
_-_ small ones in the colonoscopy
A

1
villous
high grade
3-9

82
Q

When finding 3-9 small adenomas-> repeat ___ every __ years

A

colonoscopy

3

83
Q

When finding >10 small adenomas-> repeat ___ every __ year + ___ study

A

1

genetic