Chapter 17- Small Intestine And Colon Cancers Flashcards

1
Q

What is the most common neoplastic polyp

A

Adenoma, which is able to progress to cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

When are colonic hyperplastic polyps commonly discovered

A

60/70s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the cause of hyperplastic polyps and what is the prognosis

A

Piling up of goblet cells and parietal cells, but do not have malignant potential

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What location are hyperplastic polyps most commonly found

A

Left colon

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the histological hallmark of the hyperplastic polyps

A

Serrated surface architecture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the triad of symptoms that lead to the diagnosis of inflammatory polyps

A

Rectal bleeding, mucus discharge, inflammatory lesion on the anterior rectal wall

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is that cause of inflammatory polyps

A

Impaired relaxation of the anorectal sphincter leads to a sharp angle of the anterior rectal shelf and leads to abrasion and ulceration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the histological hallmarks of an inflammatory polyp

A
  • Mixed Inflammatory infiltrates
  • Erosion
  • epithelial hyperplasia with fibromuscular hyperplasia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Inflammatory polyps develop as part of which syndrome

A

Solitary rectal ulcer syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the cause of the formation of hamartomatous polyps

A

Germline mutations in the tumor suppressor genes or protooncogenes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the ability of harmartomous polyps to malignancy

A

There is an increased risk of cancer and they are characterized as pre-malignant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

In which patients do the juvenile polyps form

A

Patients younger than 5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the main location of juvenile polyps and how do the typically preset

A

Rectum and present with rectal bleeding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are complication of juvenile polyps

A
  • Intussusception
  • Intestinal obstruction
  • polyp prolapse
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Patients with autosomal dominant syndrome of juvenile polyposis commonly have what characteristic of polyps and what is the treatment

A

Multiple (3 to 100) and must have colectomy to prevent perforation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the extraintestinal malformation of juvenile polyposis

A

Pulmonary arteriovenous malformation and other congenital abnormalities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What are the morphological findings of juvenile polyps

A

Pedunculated, smooth surfaced, reddish lesions with characteristic cystic spaces after sectioning, usually filled with mucin and inflammatory debris

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the most common mutation found in juvenile polyps

A

SMAD4, which codes for the BMPR1A of the TGF pathway

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Patients with juvenile polypropsis are most at risk for which condition

A

Development of colonic adenocarcinoma (30-50% of patients)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is the clinical presentation of pests-jeghers syndrome

A

Multiple GI hamartomatous polyps and mucocutaneous hyperpigmentation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What are the characteristics of the mucocutaneous hyperpigmentation seen in Peutz-Jeghers syndrome

A

Dark blue, brown macules on the lips, nodules, buccal mucosa, hands, genitals and perianal regions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What is the complication seen with Peutz-Jeghers polyps

A

Can cause intussuseption and multiple malignancies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Which tumors are monitored for in those with Peutz-Jeghers syndrome

A
  • Sex cord tumors of the testes (birth)
  • gastric and small intestine cancers (late childhood)
  • colon, pancreatic, breast, lung, ovarian, and uterine cancer (20s)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the mutation in Peutz-Jeghers

A

Loss of function mutation in STK11

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
What is the histological finding in Peutz-Jeghers syndrome
Arborizing network of connective tissue, smooth muscle
26
What are colorectal adenomas characterized by
Presence of epithelial dysplasia
27
What are the histological hallmarks for epithelial dysplasia in colon polyps
Nuclear hyperchromasia, elongation, and stratification
28
How are sessile serrated adenomas secreted from the hyperplastic polyps
Located on the right side of the colon
29
What are the histological findings of the sessile serrated adenomas
Have malignant potential, but tend to not have the cytological features of dysplasia -have the serrated architecture through the full length of the glands, including the crypt base, dilation and lateral growth
30
What are the histological characteristics of the intramucosal carcinoma
Dysplasia epithelial cells breach the membrane to invade the lamina propria
31
What is the malignant potential of intramucosal carcinoma
Non metastatic because the lymphatic channels are absent in the colonic mucosa
32
What is the most important characteristic of colorectal adenomas that correlates with malignancy
Size, but there is some with high grade dysplasia
33
What is the hereditability of Peutz-Jeghers syndrome
Autosomal dominant
34
What is the hereditability of Familial adenomatous polyposis
Autosomal dominant
35
Which mutation and pathway is affected in Familial adenomatous polyposis
APC for Wnt pathway
36
How many polyps are present for Familial adenomatous polyposis tobe diagnosis
At least 100, but may be 1000s
37
Patients with Familial adenomatous polyposis are guaranteed to get which condition
Colorectal adenocarcinoma
38
What is the treatment for patients with Familial adenomatous polyposis
Prophylactic colectomy
39
Despite removal of the colon, patients with Familial adenomatous polyposis develop adenomas in which location
Adjacent to the ampulla of Vater in the stomach
40
Which extraGI manifestation is commonly seen at birth in patients with Familial adenomatous polyposis
Congenital hypertrophy of the retinal pigment epithelium
41
What is the condition called when Familial adenomatous polyposis also have a mutation in MYH gene
Autosomal recessive MYH associated polyposis
42
What are the other names for Hereditary non-polyposis colorectal cancer
HNPCC | Lynch syndrome
43
What is the most common Syndromic form of colon cancer
HNPCC
44
In patients that have HNPCC, what cancers are common
Colorectal, endometrium, stomach, ovaries, urease, brain, small bowel, pancreas, and skin
45
What are the clinical presentations that can give away HNPCC patients
Colon cancers at a younger age and are located on the right side
46
What is the most common malignancy of the GI tract
Adenocarcinoma of the colon
47
What is the relative amount of tumors in the small intestine
Very rare
48
What dietary factors are most related to increased risk of colorectal cancer
Low intake of unabsorbable vegetable fiber and high intake of refined carbs and fat
49
How do NSAIDs have a protective effect on colorectal cancer development
Inhibition of COX2, which is over-expressed in adenocarcinomas
50
In colorectal cancer, what is the process of formations with the mutations that are the “hits”
``` First hit-loss of first APC Second hit-Loss of second APC and beta catenin Subsequent: -Protoonogene mutations in KRAS -TP53 -SMAD ```
51
What is the role of APC in the Wnt pathway
Negative regulator of Beta-catenin
52
Where in the stage of colorectal cancer do mutations in TP53 occur
Late
53
In patients with DNA mismatch repair deficiency, mutations occur in which areas
Microsatallite instability (MSI)
54
In colorectal cancers without mutations in DNA mismatch repair, what is commonly seen
CpG island hypermethylation phenotype (CIMP)
55
In those colorectal cancers with CIMP, what is the promoter region commonly affected
MLH1, with mutations in BRAF region
56
What are the mutations in the colon cancers with increased CpG methylation wihtoutthe microsatallite instability
KRAS mutation
57
Invasive carcinomas with microsatellite instability have which characteristics
-Mucinous differentiation and peritumoral lymphocytic infiltrates i the right side of the colon
58
How can tumors with microsatellite instability be recognized histologically
-Absence of Immuno histological staining for mismatch repair proteins or by molecular genetic analysis of sequences
59
What is a high risk for patients with HNPCC
Second malignancies of the colon and other organs
60
What are the characteristics of the adenocarcinomas in the proximal colon
Polyposis, exophytic masses, rarely causing obstruction
61
What are the characteristics of adenocarcinomas of the distal colon
Annular lesions with “napkin ring lesions” with lumen narrowing
62
Which location is common to see “napkin ring” and luminal narrowing
Distal colon
63
What is the clinical appearance of patients with Cecil and right sided colon cancers
Fatigue and weakness due to iron deficiency anemia
64
What are the clinical presentations of the patients with left sided colon adenocarcinomas
Occult bleeding, bowel habit changes, cramping, and left lower quadrant discomfort
65
What are the prognostic factors for colorectal cancers
-Depth of invasion and lymph node metastases
66
What is the most common site of metastasis in colorectal cancers
Liver
67
What causes condylomata acuminatum
HPV