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colorectal carcinoma
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
inherited condition causing bowel
cancer
1.polyposis syndromes
2.hereditary non polyposis colorectal cancer
(HNPCC)- low polyp but high risk to get CA
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)
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
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.
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
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
 rectal bleed
 tenesmus
 perforation
SIGN
cachexia
low
supraclavicular lymp node enlarge
mass/ liver/ ascitis
 rectal examination mandatory
Investigations
• Colonoscopy (best), look for synchronous
lesions -Alternative: air contrast barium enema
(“apple core” lesion) + sigmoidoscopy
• FBC
• Metastatic workup: CXR, abdominal
CT/ultrasound
• Bone scan, CT head only if lesions suspected
• Labs: CBC, urinalysis, liver function tests, CEA
(before surgery baseline)
barium enema
capsule
staging
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
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
Local Excision, Resection Anastomosis
Resection and Colostomy
Thank You
Kingsoft Office
published by www.ksosoft.com @Kingsoft_Office
kingsoftstore

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Colorectal carcinoma

  • 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
  • 9.  rectal bleed  tenesmus  perforation SIGN cachexia low supraclavicular lymp node enlarge mass/ liver/ ascitis  rectal examination mandatory
  • 10.
  • 11. Investigations • Colonoscopy (best), look for synchronous lesions -Alternative: air contrast barium enema (“apple core” lesion) + sigmoidoscopy • FBC • Metastatic workup: CXR, abdominal CT/ultrasound • Bone scan, CT head only if lesions suspected • Labs: CBC, urinalysis, liver function tests, CEA (before surgery baseline)
  • 14.
  • 15.
  • 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
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