Bowel Path IV Flashcards
lymphoid polyp
non-neoplastic
adenoma
adenomatous polyp
neoplastic
most common adenoma
tubular adenoma - small and pedunculated
greater than 4cm diameter polyp
40% chance contain foci of cancer
epithelial dysplasia
in adenoma
is pre-malignant
tubular adenoma
neoplastic
pedunculated
velvety surface
have small round tubular glands
villous adenomas
larger and sessile - covered in villi
sessile serrated adenomas
like hyperplastic polyp
-but more common in right colon
hyperplastic polyp vs. sessile serrated adenoma
serrated architecture throughout in a sessile serrated adenoma
-also in right colon
only on surface of hyperplastic polyp
malignant risk
larger polyp
more epithelial dysplasia
villous > tubular
APC/WNT pathway
typical adenocarcinoma of colon
both familial and sporadic colon cancer
FAP
100% patients get colon cancer if don’t do anything hundreds to thousands of polyps
microsatellite instability
mutation of MSH2 or MLH1 gene result in loss of enzymes in repair of damaged DNA - accumulation of microsatellite repeats
- mutation in TGF-beta receptor
- BAX genes
- BRAF gene
seen with HNPCC
-MLH1 and MSH2
familial adenomatous polyposis
auto dominant
-500-2500 colon polyps
colon cancer in 100% by age 30
most have APC gene defect, some MYH
HNPCC
lynch syndrome
hereditary non-polyposis colorectal cancer
auto dom
colon ca at young age
right sided and mucinous
microsatellite instability due to mismatch repair gene defect
CHRPE
congeintal hyperplasia of retinal pigmented epithelium
newborn with FAP
1st indication of mutation
colon carcinoma
common
clinical sx - mild abdominal discomfort, fatigue, weight loss, anemia
elevated CEA
with strep bovis
majority left sided
diet, smoking, alcohol, adenoma hx, black, older age
iron deficiency anemia in older man or postmenopausal woman
GI cancer - unless proven otherwise
path of colon carcinoma
requires multiple hits
two pathways:
- classic -APC/beta catenin - majority
- microsatellite instability - DNA mismatch repair defect
microsatellite instability
DNA mismatch repair defect
in colon carcinoma
majority of colorectal neoplasias
sporadic 97%
familial 3%