Intestinal neoplasia Flashcards
(43 cards)
Name the parts of the small intestine
Duodenum
Jejunum
Ileum
Duodenum features and function
- shortest region
- retroperitoneal
- starts at pyloric shincter and is C-shaped tube
- Duodenum means 12 - named because it is as long as the width of 12 fingers
Function: Digestion
Jejunum features and function
- 1m long extends to ileum
- jejunum means “empty” which is how it is found at death
Function: Absorption
Ileum features and function
- 2m long joins large intesting at a smooth muscle sphincter called ileocecal spinter
Primary functions of the small intestine
- further digestion of food, aided by pancreatic enzymes (forproteins) and bile (for fat).
- Lipids, peptides and sugars are all absorbed in the intestine
How long is the small intestine?
3m
Histology of the small intestine
- mucosa
- simple collumnar epithelium
- contains:
- absorptive cells - digest and absorb nutrients
- goblet cells - secrete mucus
- Deep crevices
- intestinal glands or crypts of liberkuhn - secrete intestinal juice
- submucosa (loose connective tissue),
- contains brunner gland - secrete and alkaline mucus that helps neutralise gastric acid in the chyme
- muscularis propria (thick muscle to move food),
- subserosal fat/adventitial fat (depending on location)
Which features of the small intestine Increase the surface area?
Circular folds or plica - folds of mucosa and submucosa, permanent ridges, near porximal portion of duodenum that enhance the surface area
Villi- finger like projections of mucosa, increase the surface area
Microvilli- projecions of apical(free membrane) of the absorptive cells on villi
Which ducts does the smalll intestine receive?
- Pancreatic dunct
- Bile duct
Controlled by the Spincter of oddi
- muscular valve that controls the flow of digestive juices (bile and pancreatic juice) through the ampulla of Vater into the second part of the duodenum.
Name the Parts of the large intestine
Features of the large intestine
- 1.5 m long extends from ileum to anus
- attached to posterior abdominal wall by mesocolon( double layer of periotenum)
Histology of the large intestine
- Mucosa
- simple collumnar epithelium
- absorptive
- goblet cells
- simple collumnar epithelium
- submucosa
- Musculars (CILO)
- Taenia coli - three separate longitudinal ribbons of smooth muscle on the outside of the ascending, transverse, descending and sigmoid colons. -ongtiudinal contraction
- Haustra - small pouches caused by sacculation, which give the colon its segmented appearance- circular contraction
Main function of the large intestine?
- absorption of water and electrolytes,
- Ileo-caecal valve prevents large intestinal contents passing back into small intestine – significant if obstruction nearby
Blood supply of the GI tract
3 main vessels all arising from the abdominal aorta
Epidemiology of Colorectal cancer
- Lifetime risk
- 1 in 16 for men (6%)
- 1 in 20 for women (5%)
- Overall 50% 5-year survival rate
Risk factors for colon cancer
- increasing age
- smoking (2-3 increased risk)
- Diseases:
- previous CRC
- IBD: Crohns/ UC
- Diet- low in fibre, high in red meat, processed meat
- reduced exercise
- increased alcohol intake
Pathogenesis of adenoma-carcinoma sequence
- Normal colon is exposed to DNA damage e.g. from bile acids / slow transit of stool etc.
- Accumulate mutations or may have inherited some mutations:
- APC / DCC – tumour suppressor genes
- Activation of oncogenes e.g. K-ras
- Adenomas – dysplastic but BENIGN neoplasms of glandular origin - NOT yet cancer as contained within mucosa
- Further mutations; basement membrane breached - adenocarcinoma
What are polyps?
Benign overgrowths in mucous membranes
- ricks of malignant change is related to number and size
- sessile polyps tend to develop into cancer and more often than peduculated polyps
Clinical features of benign disease
most andeomatous lesions have to clinical signs and are picked up on screening
Management of benign disease
Endoscopic mucosal resection (EMR) – this is a technique to remove polyps by colonoscopy. Upon discover of one or more polyps, colonoscopy, and subsequent EMR is advisable, whereby all visible lesions should be removed.
The patient should then be given regular and lifelong surveillance (every 3-5 years up to the age of 75) to check for the development of more polyps and / or colorectal cancer.
50% of patients will develop further polyp
Malignant potentials of adenomas
- size
- number
- histological type
Differential of adenomas
- Hyperplastic (metaplastic) polyps
- Hamartomatous polyps – normal tissue, disorganised in structure
- Inflammatory polyps – resulted from overgrowth as part of a healing response
- Submucosal lesions- e.g.lipoma, leiomyoma
Types of colorectal cancer
Familial adenomatous polyposis (FAP)
Hereditary Non-polyposis Colon cancer (HNPCC)
Familial adenomatous polyposis (FAP)
- Due to autosominal dominant APC gene (tumour suppressor gene) or Autosomal recessive MUTYH gene
- ‘Carpet’ of polyps – 1000s!
- Not common
- Linked to retinoblastoma gene so use opthalmoscopy to confirm diagnosis
- Mechanism: Via phosphorylation of beta-catenin, the APC protein which controls activation of a variety of transcription factors within cells.. Affects expression of a variety of genes thatchange proliferation and differentiation of cells