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Tumors of Intestine s. Introduction. Overall, colorectal cancer ranks second only to bronchogenic carcinoma among the cancer killers. Adenocarcinomas constitute the vast majority of colorectal cancers and represent 70% of all malignancies arising in the gastrointestinal tract. T erminology.
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Introduction • Overall, colorectal cancer ranks second only to bronchogenic carcinoma among the cancer killers. • Adenocarcinomas constitute the vast majority of colorectal cancers and represent 70% of all malignancies arising in the gastrointestinal tract.
Terminology • •A polyp is a tumorous mass that protrudes into the lumen of the gut; traction on the mass may create a stalked or pedunculated polyp. • Alternatively the polyp may be sessile, without a definable stalk. • •Non-neoplastic Polyps • abnormal mucosal maturation, • inflammation • do not have malignant potential (excl.Peutz-Jeghers) • •NeoplasticPolyps: • adenomatous polyps, or adenomas, • precursors of carcinoma.
Non-neoplastic (benign) Polyps • Hyperplastic polyps • Hamartomatous polyps • Juvenile polyps • Peutz-Jeghers polyps • Inflammatory polyps • Lymphoid polyps
Neoplastic epithelial lesions • Benign lesions: • Neoplastic polyp • Adenoma • Malignant lesions: • Adenocarcinoma • Carcinoid tumor • Anal zone (anorectal) carcinoma • Mesenchymal lesions (benign/malignant) • Lymphoma
Common Hyperplastic polyps Adults Rectosigmoid Multiple Nipple-like, Small protrusions (5 mm) Abundant crypts. Juvenile polyps Children Rectum Single Round mass 1-3 cm Dilated cystic glands. Non-neoplastic (benign) Polyps
Hyperplastic polyp Polyps Juvenile polyp
Sessile Pedunculated
Small-pedunculated; large-sessile Colon Familial predisposition Risk of carcinoma Subtypes: Tubular Villous Tubulovillous Malignancy: Rare: tubular adenoma less than 1 cm High: sessile villous adenomas more than 4 cm Dysplasia: villous adenomas. Adenomas
Tubular adenomas: Colon (rectosigmoid) Small-sessile; large-pedunculated Stalk is covered by normal mucosa Tumor is composed of neoplastic epithelium Intramucosal Ca or invasive Ca. Villous adenomas: Rectum/rectosigmoid Larger than tubular Sessile Cauliflower-like Dysplasia Ca. Tubulovillous adenomas: Peduculated or sessile Mix of tubular and villous patterns Dysplasia Malignancy.
Peutz-Jeghers Syndrome Multiple polyps (polyposis coli) large, firm polyps with a tree-like structure distinctive freckles on thelips, palms, and genitals risk for colon cancer. Turcot's syndrome Multiple polyps brain tumors. Gardner's syndrome Multiple polyps minor birth defects risk for other tumors (notably mesenchymal). Cowden's syndrome Multiple polyps Risk of tumors of: Thyroid Breast Uterus Skin. Familial polyposis syndromes
Small Intestine tumors: • Small intestine -75% but tumors – 3-6% • Benign tumors (common) • Adenoma(25%), lipoma & leiomyoma. • Malignant tumors (rare; <1%) • Adenocarcinoma of Duodenum or Jejunum, Carcinoid, Lymphoma, Sarcoma • Present at late stage, 70% 5 year survival.
Classification • Non neoplastic polyps • Hyperplastic, lymphoid & hamartomatous • Inflammatory • Neoplastic – epithelial • Benign – Adenoma(ampulla of Vater) • Malignant – Adenocarcinoma, carcinoid • Neoplastic – Mesenchymal • Benign - Lipoma, leiomyoma, neuroma, angioma • Malignant – Leiomyosarcoma, liposarcoma. • Lymphoma
Benign tumors: Lipoma • Most common • Mature adipose tissue
Napkin-ring or polypoid Duodenum (ampulla of Vater’s) Spreading: Regional lymph nodes Liver Obstructive jaundice. Adenocarcinoma
Colorectal carcinoma • Adenocarcinomas (98%) • often arises in one of the benign neoplastic colonic polyp • risk factors • (1) mild hereditary defects in anti-oncogenes lost in colon cancer, • (2) years of eating the typical western diet. • Low content of vegetables • High content of refined carbohydrates • High content of fat (animal) • Low content of micronutrients (vitamins A, C, E).
Morphology Proximal colon tumors: polypoid Cecum and ascending colon: exophytic Distal colon: napkin-ring Progression: slow (years) Types: Gut: Adenocarcinoma Mucin production Anal zone: Squamous cell carcinoma Spreading: Regional lymph nodes Liver
2% of colorectal malignancies. Origin:Neuroendocrine cells (paracrine, Kulchitsky, enterochromaffin, neurosecretory, chromaffin) Location: gut (common in appendix) pancreas or peripancreatic tissue, lungs, biliary tree liver. Rectal and appendiceal carcinoidsalmost never metastasize The classic carcinoid syndrome (serotonin) (1) wheezing (asthmatic); (2) flushing (vasomotor); (3) fibrosis (cardiac, pulmonic, pleural, pelvic); (4) intestinal hypermotility. Carcinoid Tumors
Midgut carcinoids: small intestinal, appendiceal, most colonic carcinoids. These are usuallyargyrophil (hormonally active). Foregut carcinoids: lung, duodenal, biliary carcinoids. These are almost never argyrophil (hormonally inactive).
Less common than carcinomas Westernlymphomas are usually familiar B-cell lymphomas Mediterranean lymphomas usually feature plasmacytoid differentiation (a subset is alpha-heavy chain disease). Sprue-associated lymphoma exhibits T-cell markers Gastrointestinal lymphoma