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TUMORS OF COLON
• COLORECTAL POLYPS:
o any growth or mass protruding from mucus
membrane into lumen.
o Large intestine > small intestine
o Recto - Sigmoid colon > proximal colon
o Classification :
1. Non – neoplastic
2. Neoplastic
Non – neoplastic polyps:
Types:
1. hyperplastic / metplastic polyps
2. Hamartomatous polyps
3. Inflammatory polyps
4. Lymphoid polyps
HYPERPLASTIC POLYPS:
• Most common
• Rectosigmoid
• Any age. Common: 60 – 70 yrs
• Areas of hyperplasia and areas of metaplasia
present
• Polyp + adenoma = malignant; polyp = benign
G / A:
• Multiple
• Sessile
• Smooth surface
• Small : < 0.5 cm
M / E:
• Long and cystically dilated glands lined by normal
epithelium
HAMARTOMATOUS POLYPS :
• Tumor like lesions containing abnormal mixture of
cells indegenous to that part.
• 2 types:
1. Peutz – Jeghers Polyps and Polyposis:
• Autosomal dominant defect
• Character: hamartomatous intestinal polyposis
with melanotic pigmentation on lips, mouth and
genitalia
G / A:
• Variable size. Common : large
• Multiple
• Pedunculated
M / E:
2. Juvenile / retention polyps:
• Hamartomatous polyps occuring in children below
5 years
• Solitary
• Common in rectum
G / A:
• Spherical
• smooth surfaced
• Pedunculated
• 2 cm = dm
M / E:
• Cystically dilated glands containing mucus
• Normal mucus secreting epithelial cell lining
• If chronic ulceration of surface is present then
stroma shows inflammatory cell infiltrates.
INFLAMMATORY POLYPS:
• Re-epithelization of undermined ulcers and
overhanging margins in inflammatory bowel
diseases like ulcerative colitis and Crohn’s
disease.
G / A:
1. Multiple
2. Cylindrical to rounded
3. Minute nodules – several centimeters
M / E:
• Centre of the polyp contains connective tissue
core that contains some inflammatory cell
infiltrates and are covered by thin layer of
regenerating epithelial cells and cystically
Lymphoid polyps:
• Reactive hyperplasia of lymphoid tissues.
• Prominent in rectum and terminal ileum
• Also called rectal tonsils
G / A:
• Solitary / multiple
• Tiny
• Elevated lesions
M / E:
• Prominent lymphoid follicles with germinal
centres located in mucosa and submucosa
• Inflammed epithelial covering
 Neoplastic polyps:
• Colorectal adenomas which have potential for
malignant change
• 3 main varieties
1. Tubular
2. Villous
3. Tubulovillous
TUBULAR ADENOMA / ADENOMATOUS
POLYP:
• most common
• > 30 years
• Male > female
• Common in distal colon and rectum
• Asymptomatic / rectal bleeding
G / A:
• single or multiple
• sessile or pedunculated
• less than 1 cm or more
• large, spherical masses with an irregular
M / E:
• Branching tubules embedded in the lamina
propria.
• The lining epithelial cells are of large intestinal
type with diminished mucus secreting capacity,
large nuclei and increased mitotic activity.
• Variable degree of cytologic atypia ranging from
‘carcinoma in situ’ to frank adenocarcinoma
VILLOUS ADENOMA / VILLOUS PAPILLOMA:
• Less common.
• >60 years
• Both men and women.
• Often in the distal colon and rectum.
• invariably symptomatic
• rectal bleeding, diarrhoea and mucus being the
common features.
• The presence of severe atypia, carcinoma in
situ and invasive carcinoma are seen more
frequently.
G / A:
• round to oval exophytic masses
• sessile
• 1 to 10 cm or more in diameter.
• surface may be haemorrhagic or ulcerated.
M / E:
• many slender, finger-like villi, which appear to
arise directly from the area of muscularis
mucosae.
• Each of the papillae has fibrovascular stromal
core that is covered by epithelial cells varying
from apparently benign to anaplastic cells.
TUBULOVILLOUS ADENOMA / PAPILLARY
ADENOMA / VILLOGLANDULAR ADENOMA:
• intermediate form of pattern between tubular
adenoma and villous adenoma
• most common
• > 30 years
• Male > female
• Common in distal colon and rectum
• Asymptomatic / rectal bleeding
G / A:
• single or multiple
• sessile or pedunculated
• less than 1 cm or more
• large, spherical masses with an irregular surface.
M / E:
• Branching tubules embedded in the lamina
propria.
• The lining epithelial cells are of large intestinal type
with diminished mucus secreting capacity, large
nuclei and increased mitotic activity.
• Variable degree of cytologic atypia ranging from
‘carcinoma in situ’ to frank adenocarcinoma
 OTHER BENIGN TUMORS ARE:
1. Leiomyomas
2. Leiomyoblastoma
3. Neurilemmoma
4. lipoma
5. vascular tumours - haemangioma,
lymphangioma
MALIGNANT TUMORS :
1. Colorectal Carcinoma
2. leiomyosarcoma
3. malignant lymphoma
4. Hindgut carcinoids may occur in the rectum
and colon
COLORECTAL CARCINOMA:
• commonest form of visceral cancer
• Age : 60 years and above
• Common in males than females
ETIOLOGY:
1. Geographic variations
2. Dietary factors.
3. Adenoma-carcinoma sequence.
4. Hereditary non-polyposis colonic cancer
(HNPCC or Lynch syndrome)
5. Other factors
GROSS ANATOMY:
• Right-sided colonic growths:
• large
• cauliflower-like, soft and friable masses
projecting into the lumen (fungating polypoid
carcinoma).
• Left-sided colonic growths:
• napkin-ring configuration - they encircle the
bowel wall circumferentially with increased
fibrous tissue forming annular ring
• central ulceration on the surface with slightly
elevated margins (carcinomatous ulcers).
• However, early lesion in left as well as right
colon are small, button-like areas of elevation.
Microscopically:
• the appearance of right and left-sided growths is
similar.
• adenocarcinomas of varying grades of
differentiation, most are mucin-secreting colloid
carcinomas while some are uncommon microscopic
patterns like undifferentiated carcinoma, signet-ring
cell carcinoma, and adenosquamous carcinomas
seen in more distal colon near the anus.
• The histologic grades indicating the degree of
differentiation are: well-differentiated, moderately
differentiated and poorly-differentiated
SPREAD:
1. Direct spread
2. Lymphatic spread
3. Haematogenous spread
CLINICAL FEATURES:
1. Melaena
2. Change in bowel habits, more often in left-
sided growth
3. Cachexia
4. Anorexia
5. Anaemia, weakness, malaise.

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Tumors of colon

  • 2. • COLORECTAL POLYPS: o any growth or mass protruding from mucus membrane into lumen. o Large intestine > small intestine o Recto - Sigmoid colon > proximal colon o Classification : 1. Non – neoplastic 2. Neoplastic
  • 3. Non – neoplastic polyps: Types: 1. hyperplastic / metplastic polyps 2. Hamartomatous polyps 3. Inflammatory polyps 4. Lymphoid polyps
  • 4. HYPERPLASTIC POLYPS: • Most common • Rectosigmoid • Any age. Common: 60 – 70 yrs • Areas of hyperplasia and areas of metaplasia present • Polyp + adenoma = malignant; polyp = benign G / A: • Multiple • Sessile • Smooth surface • Small : < 0.5 cm M / E: • Long and cystically dilated glands lined by normal epithelium
  • 5.
  • 6. HAMARTOMATOUS POLYPS : • Tumor like lesions containing abnormal mixture of cells indegenous to that part. • 2 types: 1. Peutz – Jeghers Polyps and Polyposis: • Autosomal dominant defect • Character: hamartomatous intestinal polyposis with melanotic pigmentation on lips, mouth and genitalia G / A: • Variable size. Common : large • Multiple • Pedunculated M / E:
  • 7.
  • 8. 2. Juvenile / retention polyps: • Hamartomatous polyps occuring in children below 5 years • Solitary • Common in rectum G / A: • Spherical • smooth surfaced • Pedunculated • 2 cm = dm M / E: • Cystically dilated glands containing mucus • Normal mucus secreting epithelial cell lining • If chronic ulceration of surface is present then stroma shows inflammatory cell infiltrates.
  • 9.
  • 10. INFLAMMATORY POLYPS: • Re-epithelization of undermined ulcers and overhanging margins in inflammatory bowel diseases like ulcerative colitis and Crohn’s disease. G / A: 1. Multiple 2. Cylindrical to rounded 3. Minute nodules – several centimeters M / E: • Centre of the polyp contains connective tissue core that contains some inflammatory cell infiltrates and are covered by thin layer of regenerating epithelial cells and cystically
  • 11.
  • 12. Lymphoid polyps: • Reactive hyperplasia of lymphoid tissues. • Prominent in rectum and terminal ileum • Also called rectal tonsils G / A: • Solitary / multiple • Tiny • Elevated lesions M / E: • Prominent lymphoid follicles with germinal centres located in mucosa and submucosa • Inflammed epithelial covering
  • 13.
  • 14.  Neoplastic polyps: • Colorectal adenomas which have potential for malignant change • 3 main varieties 1. Tubular 2. Villous 3. Tubulovillous
  • 15. TUBULAR ADENOMA / ADENOMATOUS POLYP: • most common • > 30 years • Male > female • Common in distal colon and rectum • Asymptomatic / rectal bleeding G / A: • single or multiple • sessile or pedunculated • less than 1 cm or more • large, spherical masses with an irregular
  • 16.
  • 17. M / E: • Branching tubules embedded in the lamina propria. • The lining epithelial cells are of large intestinal type with diminished mucus secreting capacity, large nuclei and increased mitotic activity. • Variable degree of cytologic atypia ranging from ‘carcinoma in situ’ to frank adenocarcinoma
  • 18. VILLOUS ADENOMA / VILLOUS PAPILLOMA: • Less common. • >60 years • Both men and women. • Often in the distal colon and rectum. • invariably symptomatic • rectal bleeding, diarrhoea and mucus being the common features. • The presence of severe atypia, carcinoma in situ and invasive carcinoma are seen more frequently.
  • 19. G / A: • round to oval exophytic masses • sessile • 1 to 10 cm or more in diameter. • surface may be haemorrhagic or ulcerated. M / E: • many slender, finger-like villi, which appear to arise directly from the area of muscularis mucosae. • Each of the papillae has fibrovascular stromal core that is covered by epithelial cells varying from apparently benign to anaplastic cells.
  • 20.
  • 21. TUBULOVILLOUS ADENOMA / PAPILLARY ADENOMA / VILLOGLANDULAR ADENOMA: • intermediate form of pattern between tubular adenoma and villous adenoma • most common • > 30 years • Male > female • Common in distal colon and rectum • Asymptomatic / rectal bleeding
  • 22. G / A: • single or multiple • sessile or pedunculated • less than 1 cm or more • large, spherical masses with an irregular surface. M / E: • Branching tubules embedded in the lamina propria. • The lining epithelial cells are of large intestinal type with diminished mucus secreting capacity, large nuclei and increased mitotic activity. • Variable degree of cytologic atypia ranging from ‘carcinoma in situ’ to frank adenocarcinoma
  • 23.
  • 24.  OTHER BENIGN TUMORS ARE: 1. Leiomyomas 2. Leiomyoblastoma 3. Neurilemmoma 4. lipoma 5. vascular tumours - haemangioma, lymphangioma
  • 25. MALIGNANT TUMORS : 1. Colorectal Carcinoma 2. leiomyosarcoma 3. malignant lymphoma 4. Hindgut carcinoids may occur in the rectum and colon
  • 26. COLORECTAL CARCINOMA: • commonest form of visceral cancer • Age : 60 years and above • Common in males than females ETIOLOGY: 1. Geographic variations 2. Dietary factors. 3. Adenoma-carcinoma sequence. 4. Hereditary non-polyposis colonic cancer (HNPCC or Lynch syndrome) 5. Other factors
  • 27.
  • 28. GROSS ANATOMY: • Right-sided colonic growths: • large • cauliflower-like, soft and friable masses projecting into the lumen (fungating polypoid carcinoma). • Left-sided colonic growths: • napkin-ring configuration - they encircle the bowel wall circumferentially with increased fibrous tissue forming annular ring • central ulceration on the surface with slightly elevated margins (carcinomatous ulcers). • However, early lesion in left as well as right colon are small, button-like areas of elevation.
  • 29.
  • 30. Microscopically: • the appearance of right and left-sided growths is similar. • adenocarcinomas of varying grades of differentiation, most are mucin-secreting colloid carcinomas while some are uncommon microscopic patterns like undifferentiated carcinoma, signet-ring cell carcinoma, and adenosquamous carcinomas seen in more distal colon near the anus. • The histologic grades indicating the degree of differentiation are: well-differentiated, moderately differentiated and poorly-differentiated
  • 31.
  • 32. SPREAD: 1. Direct spread 2. Lymphatic spread 3. Haematogenous spread CLINICAL FEATURES: 1. Melaena 2. Change in bowel habits, more often in left- sided growth 3. Cachexia 4. Anorexia 5. Anaemia, weakness, malaise.