GIT neoplasia patho Flashcards
what is a polyp
a fleshy protuberant growth on an epithelial surface
*some benign polyps are precancerous
difference between pedunculated and sessile polyps
- pedunculated - presence of stalk holding polyps
- sessile - no stalk
benign polyps
- fundic gland polyps
- hyperplastic polyps
what are fundic gland polyps caused by
- sporadic -> eg due to PPI inhibitor reactions/ stress
- familial -> eg FAP
*associated with reduced acidity in stomach
what does hyperplastic polyps usually precede
- chronic erosive gastritis
what are hyperplastic polyps indicative of
- regenerative response to injury
presentation of hyperplastic polyps
- surface erosions leading to bleeding
- multiple polyps present in gastric atrophy
malignant stomach carcinomas
- gastric carcinoma
- gastric adenocarcinoma
what is gastric adenocarcinoma
- malignant neoplasm showing GI
glandular epithelial differentiation
is gastric carcinoma symptomatic in early stages?
NO
*most pts are not scoped in time to discover carcinoma
clinical presentation of gastric carcinoma
- weight loss (due to VOMITING)
- abdominal pain
- dysphagia
- haemorrhage (vomit blood)
what is early gastric cancer (EGC)
- invasive cancer (gastric carcinoma) that invades no deeper than submucosa
*irrespective of lymph node metastasis
what is gastric carcinoma associated with
- asians
- JAPAN
*thus japan has mass endoscopy screening to identify gastric cancer at EGC rather than progressing to late stage gastric carcinoma
how to describe gastric carcinoma
Exophytic
- protrusion of tumour mass into lumen (ie small bump)
- early exophytic tumour does not erode submucosa, late tumour will erode into submucosa and even into smooth muscle
Flat/ depressed
- no obvious tumour mass within mucosa
- early flat tumour does not erode submucosa, late tumour will erode into submucosa and even into smooth muscle
Excavated
- shallow/ deeply erosive crater present in walls of stomach
- early vs late excavated tumour differs in submucosal vs submucosal + muscle erosion as well
types of gastric adenocarcinoma (2)
- intestinal type adenocarcinoma (MAJORITY)
- diffuse type adenocarcinoma
describe intestinal type adenocarcinoma
- arise from complete-type intestinal metaplasia
- genetic alterations resemble colonic carcinoma
describe diffuse type adenocarcinoma
- arise from gastric foveolar epithelium
presentation:
- broad region of gastric wall extensively infiltrated by malignancy -> create RIGID, THICKENED “leather bottle” termed linitis plastica
growth and spread of gastric carcinomas
local infiltrations:
- pylorus and antrum > cardia lesser curve > greater curvature
metastasis
- distant metastases to adrenal gland, peritoneum, ovary, spleen
- metastases to SUPRACLAVICULAR NODES (VIRCHOW’S NODE)
intestinal adenomas definition and types
- benign epithelial neoplastic polyps composed of proliferating neoplastic GLANDS
types (different growth patterns)
- tubular adenoma
- tubulovillous adenoma
- villous adenoma
what is Peutz-Jeghers Syndrome associated with
- POLYPS (HAMARTOMATOUS) in GI tract
- increased PIGMENTATION around lips, genitalia, feet & hands
- YOUNG CHILDREN
- little malignant potential
- GENETIC related
colorectal cancer (malignant) imaging
- polypoidal, ulcerated appearance
- CIRCUMFERENTIAL growth (grows around entire circumference of colon -> constricts colon lumen greatly -> aka APPLE CORE lesions
colorectal cancer presentation
- abdominal pain due to intestinal obstruction
- UNEXPLAINED ANEMIA
- spurious diarrhea (alternate diarrhea & constipation due to mucus accumulation and seeping through thin lumen [diarrhea] and faecal obstruction from thin lumen [constipation]
- pneumaturia (gas in urine) due to bladder invasion
colon adenocarcinoma epidemiology
- cancer begins in the cells of colonic crypts and spreads first through the wall of the colon and potentially into the lymphatic system and other organs
what causes colorectal cancer
- stems from colon polyps that turn cancerous
- individuals that develop multiple polyps -> higher risk of colon cancer
hereditary causes of colorectal cancer
- lynch syndrome
- classic FAP (younget age of cancer onset)
- attenuated FAP
what is FAP caused by
- autosomal dominant inherited syndrome
- inactivating mutation in APC gene chromosome 5q21 -> disrupt function of tumour suppressor gene at birth -> cancer
what are carcinoids
- neuroendocrine tumours
effects of carcinoid metastases
- carcinoid syndrome (from over production of substances like serotonin
most frequent sarcoma of GI tract
- GIST (gastrointestinal stromal tumour)
gastrointestinal stromal tumour (GIST) presentations
- polypoidal intramural tumour masses, ulcerate overlying GI mucosa
- rare: separate masses within mesentery
markers used for GIST diagnosis
- CD117
- CD34