Path Notes: Intestinal Polyps: Non-Neoplastic Polyps******** Flashcards
What are intestinal polyps? What is their morphology?
Intestinal polyps are masses that extend into the intestinal lumen.
Morphologically, they are:
- Sessile (no stalk)
- Pedunculated (with stalk)
What are the two pathological types of intestinal polyps? (Just name them)
- Non-neoplastic
Can arise from abnormal maturation, inflammation or architecture. There is no malignant potential per se. - Neoplastic
What are some examples of Non-neoplastic Intestinal polyps, describe them>
Non-Neoplastic polyps can arise from abnormal maturation, inflammation or architecture
Examples:
1. Inflammatory Polyp = May form from chronic cycles of injury and healing
- Hyperplastic Polyp = Associated with changes in cell turnover - decreased epithelial cell turnover leads to accumulation of mature cells on surface
- Hamartamotous Polyp = Tumour-like growth composed of mature tissue which is normal to the area in which the polyp has arisen. E.g. of this is Juvelile Polyp (which can be sporadic or syndromic). Or Peutz-Jeghers Polyp (rare AD syndrome)
What are Neoplastic Polyps?
A common type of neoplastic polyp is an adenoma (adenomatous polyp). These can progress to cancer
Describe Hyperplastic Polyps:
Account for 90% of non-neoplastic intestinal polyps
Unknown aetiology
Typically rectosigmoid
Very common
Associated with changes in cell turnover: decreased epithelial cell turnover leads to an accumulation of mature cells on the surface.
Describe Hamartomatous Polyps (not including subtypes)
Generally have no malignant potential - non-neoplastic intestinal polyp
80% of harmatomatous polyps develop in the rectum, but they may be scattered
What are the three subtypes of Hamatomatous Polyps?
- Juvenile Polyps (sporadic type)
- Juvenile Polyposis (syndrome)
- Peutz-Jeghers Polyps
Describe Juvenile Polyps - sporadic type. Epidemiology, macro features
AKA retention polyps
Involves hamatomatous malformation (growth that resembles a tumour that is non-neoplastic) of the mucosal epithelium and lamina propria
Typically occurs in those <5yo
Mostly occur in the rectum
Macroscopically: 1-3cm diameter Rounded smooth or slightly lobulated Stalks up to 2cm long The lamina propria bulk of the polyp contains cystically dilated glands
Describe Juvenile Polyposis syndrome. Epidemiology and maco features
Autosomal Dominant syndrome
Sometimes associated with SMAD / DZPC4 gene mutations - an intermediate signalling by TGF-B
Invovles multiple juvenile polyps: 50-100
Associated with increased risk of adenocarcinoma*
Macroscopically: 1-3 cm diameter Rounded smooth or slightly lobulated Stalks up to 2 cm long Lamina propria bulk of the polyp contains cystically dilated glands
Describe Peutz-Jhegers Polyps: Epidemiology / Pathological features
Rare autosomal dominant syndrome
Mutation of the LKB1 / STK11 gene of chromosome 19
LKB1 / STK11 is a kinase that regulates cell polarisation, growth and metabolism
Involves multiple polyps scattered throughout entire GIT - 25% in stomach, 30% in colon, 100% in small bowel
Melanotic mucosal and cutaneous pigmentation around the lips, oral mucosa, face, genitalia, palmar surfaces of the hands
The polyps have no malignant potential, but GIT adenocarcinoma can arise independently of the Peutz-Jhegers polyps.
Generally, people with Peutz-Jhegers have an increased risk of cancer of colon, pancreas, breast, lung, ovary, testes and uterus
Peuts-Jhagers Polyps: Macro and Micro features
Macroscopically:
- Polyps are large and pedunculated
- Have firm, lobulated contour
Microscopically:
- Network of of connective tissue and well developed smooth muscle extends into the polyp
- This network also surrounds normal glands