Polyps, Esophagitis, Surgical Abdomen Flashcards
(104 cards)
define polyp classifications
non-neo
neo

Smooth surface “cloud-like” appearance polyp
tx?
sessile serrated
Complete excision is recommended - due to their sessile nature and indistinct borders, special care is needed to ensure their complete removal endoscopically.
adenomas ≥10 mm in size or with villous components or high-grade dysplasia.
Advanced Adenomatous Polyps
Most common non-neoplastic polyp
•Normal cellular components but may be indistinguishable from adenomatous polyps
Hyperplastic Polyps
Look similar to tubular adenomas
Irregularly shaped islands of intact mucosa that forms as a result of mucosal ulceration and regeneration
•Seen in UC and Crohn’s Disease
Inflammatory Pseudopolyps
define high greade vs low grade dyplasia
Low-grade dysplasia – some cells are abnormal, but unlikely to spread
High-grade dysplasia- represents a step in the progression from a low-grade dysplasia to cancer - unlikely to metastasize
•applied to lesions that are confined to the epithelial layer and lack invasion into the lamina propria.
Recommend that CRC screening begin at
- age 45 in African Americans, and that colonoscopy is the preferred test - More likely to develop right sided CRC
- Age 50 for other races
CRC screening recc in
lynch syndrome
FAP
lynch
- Age 20-25 or 10 years younger then youngest affected relative
- Colonoscopy 1-2 years
- Then yearly at age 40
- Genetic testing recommended
FAP
- Age 10-12 sigmoidoscopy yearly
- Colonoscopy yearly after polyp discovered genetic testing and counseling
CRC screening reccomendations
hx of CRC
hx of adenoma
IBD
Personal Hx of CRC
- Total colon exam w/in 1 yr, repeat at 3 yrs
- Repeat 5 yrs if normal
Personal Hx of Adenoma- Repeat colonoscopy every 3-5 yrs
IBD
- Begin 8 yrs after diagnosis
- Colonoscopy every 1-2 yrs
differnetiate b/w cancer prevention vs cancer detection tests

Fecal Occult Blood Test(Stool Guaiac)
Testing stool for the presence of blood – 3 separate stools
Lowest specificity / sensitivity
•Detects ANY blood – could be from nose bleed etc
Fecal Immunochemical test (FIT)
More sensitive for colonic blood loss -Higher CRC detection rates compared to FOBT
Detection of advanced adenomas is VERY low
Fecal DNA (FIT-DNA
Looks for evidence of mutations associated molecular changes leading to malignancies – KRAS mutations, methylation biomarkers associated with neoplasia, and hemoglobin
•Full stool sample in a special collection kit
Higher specificity for CRC –Still LOW detection od adenomas
Convenient, no sedation
The definitive test for detection of precancerous adenomas and CRC
colonoscopy
Avg risk – 10 yrs
May be shorter for higher risk (3-5 yrs)
Patients who cannot take colonoscopy or who are sick –
why BAD for AAs or younger population ??
Sigmoidoscopy
•BAD for AAs or younger population as they are most likely affected by Right sided colon cancer
41-45% of CRC are on the right side and will be missed
Most colorectal cancers, regardless of etiology, arise from ____ polyps polyps
adenomatous
Currently Influence CRC Screening
- Personal or Family History of CRC or polyps
- Age
- Hereditary CRC Syndromes
Carcionembryonic antigen (CEA) level
but used to monitor progression pre-post surgery, of CRC
• indicator of Recurrence. Expect to normalize after surgery
si/sx of CRC
Change in bowel habits – 74%
Rectal bleeding/bloody stool/black stool – 51%
Anemia
tx of CRC
Surgery – Resection of primary colonic or rectal cancer is the treatment of choice in all stages (I+II ONLY surgery)
- Poorly differentiated histology
- Lymphovascular invasion
- T2 lesion, cancer at stalk margin
Chemotherapy –Stages III&IV Colon cancer
Radiation + Chemotherapy – Rectal Cancer stages II-IV
differntiate b/w iron deficency pattern vs anemia of chronic dz
iron deficency
Transferrin/TIBC – Increased
- Transferrin Sat% - low
- Ferritin* - low
anemia of chronic dz
•Transferrin/TIBC – low
- Transferrin Sat% - normal or low-normal
- Ferritin* – normal or elevated
chemo for CRC is reccomended at what stage
III
Indications to Consider Hereditary Intestinal Polyposis Syndrome
- Patient with family history of CRC affecting more than one family member.
- Personal or family history of colorectal cancer developing early age <50 years
- Personal or Family History of multiple polyps >20 cumulative!)
- Personal or family history of multiple extracolonic malignancies.
Intestinal Polyposis Syndromes
Lynch Syndrome / HNPCC
Familial Adenomatous Polyposis (FAP)