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risk factors for colorectal cancer
family history
familial adenomatous polyposis (FAP)
hereditary nonpolyposis colorectal cancer (HNPCC)
IBD
increased age
diet high in red meat, low in fibre, low in fruit and veg, calcium
alcohol
smoking
what is FAP
autosomal dominant condition involving malfunctioning of tumour suppressor genes called adenomatous polyposis coli (APC)
- results in polyps in large intestine
- potential to become cancerous
-screening annual colonoscopy from age 10-12 years
what is HNPCC
autosomal dominant condition resulting in mutations in DNA mismatch repair (MMR) genes
- patients at high risk of cancer
-screening from age 25 → 2 yearly colonoscopy
what do majority of colorectal cancers arise from
polyps
adenoma to carcinoma in the colon - molecular aspect
activation of oncogene - k-ras or c-myc
loss of tumour suppressor genes - APC, p53, DCC
defective DNA repair pathways - microsatellite instability
ALL LEAD TO CELL GROWTH PROLIFERATION APOPTOSIS
red flag symptoms that may make you consider colorectal cancer
changes in bowel habit - usually more diarrhoea
unexplained weight loss
rectal bleeding - can be mixed with stool
unexplained abdominal pain
iron deficiency anaemia
palpable abdominal or rectal mass upon examination
NICE guidelines for referral in suspected colorectal cancer
under 40 with abdominal pain AND unexplained weight loss
over 50 with unexplained rectal bleeding
over 60 with a change in bowel habit or iron deficiency anaemia
investigations for colorectal cancer
COLONOSCOPY = gold standard
radiological imaging
- CT colonography
- barium enema
- CT abdomen/pelvis
staging of colorectal cancer
Duke's staging A-D
- A = confined to mucosa and part of muscle of bowel wall
- B = extending through muscle of bowel wall
- C = lymph node involvement
- D = metastatic
more advanced the disease, the worse your outlook
TNM classification of colorectal cancer
T - tumour
- TX = unable to assess size
- T1 = submucosa involvement
- T2 = muscularis propria involvement
- T3 = involvement of subserosa and serosa but not through
- T4 = spread through serosa (4a) reaching other tissues or organs (4b)
N - nodes
- NX = can't assess
- N0 = no nodal spread
- N1 = 1-3 nodes
- N2 = 3 or more nodes
M - metastasis
- M0 = no
- M1 = yes
treatment/management of colorectal cancer
colectomy
chemotherapy
radiotherapy (rectal cancer only)
surgical resection (very early lesions)
palliative care
complications of surgery in colorectal cancer
bleeding
infection
pain
damage to nerves, vessels, bladder, ureters or bowel
post op ileus
anaesthetic risk
laparoscopic surgery converted to open surgery
leakage or failure of anastomosis
requirement for stoma
failure to remove tumour
DVT
PE
incisional hernia
intra-abdominal adhesions
screening modalities for colorectal cancer
faecal occult blood test - colonoscopy if +ve
FIT
flexible sigmoidoscopy
colonoscopy
CT colonography
normal function of colon
water and electrolyte absorption
production and absorption of vitamins K and B
storage of faeces (Rectum)
hosts gut microbiota - role in immune function and diseases
arterial supply of colon
SMA - right colic, middle colic and ileocolic arteries.
IMA - left colic, sigmoid colic arteries
Marginal artery of Drummond.
innervation of colon
T10-L1
complications of a stoma
bleeding
infection
anastomotic leak
stomach problems - ischaemia, prolapse, hernia, high output
possible impaired fertility
post op management of colorectal cancer
adjuvant chemo
- complications may delay this
surveillance CT, colonoscopy
bowel obstruction cardinal signs
abdominal pain
vomiting
absolute constipation - not flatus or faeces
abdominal distension
large intestine causes of obstruction
tumour
strictures - diverticulitis
faecal impaction
pseudo-obstruction
small intestine causes of obstruction
adhesions
hernia
importance of screening
prevention method to detect early cancers in the general population, high risk groups AND those that are symptomatic - rule out test for significant bowel disease, avoiding unnecessary colonoscopy
MAP
autosomal recessive, caused by pathogenic variants in the MUTYH base-exicsion repair gene
colorectal cancer mostly right sided and synchronous
-high risk of cancer at later age (60)
-annual colorectal surveillance commencing 18-20 years
what do patients with colorectal cancer complain of the most
-Rectal bleeding – anorectal pain, colour, mixed in stool
-Change in bowel habits (diarrhoea, constipation)
-Fatigue
-Abdominal pain - colicky
-Weight loss
-Tenesmus
-Vomiting
why is MRI important in rectal cancer
could dictate if neoadjuvant chemotherapy, radiotherapy or both required followed by surgery
when is colon cancer almost always straight to surgery?
if no metastatic disease & patient fit