This document summarizes information about colorectal carcinoma:
- It is the 3rd most common cancer and most common after age 60. Risk factors include diet, diabetes, ulcerative colitis, and genetic conditions.
- Inherited conditions like familial adenomatous polyposis (FAP) and Lynch syndrome can cause colorectal cancer. FAP causes multiple polyps developing by the teen years and cancer by age 40.
- Presenting symptoms include blood in stool, changes in bowel habits, abdominal pain, obstruction, and weight loss. Investigations include colonoscopy, imaging, and blood tests. Treatment depends on staging but may include surgery, chemotherapy, and radiation.
2. epidemiology
3rd most common
3rd of this disease arise in rectum
rare before 50( except in inherited colorectal
cancer syndromes)
common after 60
other factor: diet(low fibre , high fat,red
meat,alcohol,) , diabetic, UC, inherited genetic
condition
more common in developed (sporadic young
indian subcontinent)
reduction in dss if taken aspirin
3. inherited condition causing bowel
cancer
1.polyposis syndromes
2.hereditary non polyposis colorectal cancer
(HNPCC)- low polyp but high risk to get CA
4. polyposis syndromes
• familial adenomatous polyposis (FAP)
• AD in APC gene coz hundredss polyps develop
by mid teen.
• develop CA at age 40
• prevention : surgery in early adulthood 1.
(subtotal colectomy with ileorectal anastomosis)
2. (panproctocolectomy)
5. polyposis syndromes
peutz-jeghers syndrome
develop hamartomas polyps throughout GI tract
others features: freckles around mouth, hand,
feet, genitalia
die at 50 because - bowel intussusception
-cancer
cancer usually at
small/large/stomach/pancreas/testes and breast
6. HNPCC
Lynch syndrome
defect in mismatch repair genes which mend
damaged DNA
70% risk to get colorectal CA
indicator cancer : endometrium/ ovary/
urothelium/ small bowel / brain
when patient > 45 develop indicator cancer then
we test marker for genetic condition.
7. pathophysiology
• most CA initially exophytic(protrude into lumen)
then ulcerated and progressively invade the
muscular bowel wall. then eventually involved
serosa and surrounding structures.
• stromal fibrosis cause luminal narrowing (IO)
large bowel spread via lymphatic then blood
stream
lymphatic 1-mesenteric node 2.para aortic
nodes( duodenal obstruction)(compress bile
duct coz jaundice)
blood spread 1. liver
8. presentation
blood loss anaemia
caecum and asc colon rare cause obstruction
palpable mass in right iliac fossa
change in bowel habit
blood and mucus and loose stool
large bowel obstruction(partial and complete)
left colon because more solid
17. Treatment
• SURGERY (indicated in potentially curable or symptomatic cases
-not always in stage IV)
• Curative: wide resection of lesion (5 cm margins) with nodes and
mesentery
• Palliative: if distant spread, then local control for hemorrhage or
obstruction
• 80% of recurrences occur within 2 years of resection
• Improved survival if metastasis consists of solitary hepatic mass that
is resected
• Colectomy:
• -most patients get primary anastomosis (e.g. hemicolectomy, low
anterior resection (LAR)-
• -if cancer is below levators in rectum, patient may require an
abdominal perineal resection (APR) with a permanent end
colostomy, especially if lesion involves the sphincter complex
• -complications: anastomotic leak or stricture, recurrent disease,
pelvic abscess, enterocutaneous fistula
18. RADIOTHERAPY & CHEMOTHERAPY
• Chemotherapy (5 FU based regimens): for patients with
node-positive disease
• Radiation: for patients with node-positive or transmural
rectal cancer (pre ±post-op), not effective in treatment of
colon cancer
• Adjuvant therapy –chemotherapy (colon) and radiation
(rectum)
• Palliative chemotherapy/radiation therapy for
improvement in symptoms and survival