Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
66 Cards in this Set
- Front
- Back
circumscribed pouch of a tubular ogan
|
diverticulum
|
|
true vs. false diverticulum
|
True: pouch contains all layers (mucosa, submucosa, muscularis propria, adventitia)
false: pouch contains mucosa and submucosa that have herniated thru the muscularis propria |
|
Meckel's diverticulum: defn
|
Failure of the vitelline duct to involute.
A True diverticulum in distal ileum. |
|
What is the rule of 2s for Meckels diverticulum?
|
2% of population
2" long Located in ileum 2 feet from ileocecal valve usually presents at 2 years old |
|
Complications of Meckels diverticulum
|
Bleeding, volvulus, intussusceptions or obstruction, generally during first two years of life.
|
|
T/F approximately 50% of symptomatic Meckel's diverticula have ectopic gastric or pancreatic cells and can develop gastric ulcers in there
|
T
|
|
Hirschsprung’s Disease: defn
|
disorder of the gut which is caused by the failure of the neural crest cells (enteric ganglion cells) to migrate completely during fetal development of the intestine.
aka enteric aganglionosis |
|
Diverticular Disease of the Colon
involves (true, false) diverticula. |
False
|
|
Where are false diverticula most common?
|
sigmoid colon
|
|
Sx of false diverticula?
|
cramping pain, bleeding, and perforation
|
|
pathogenesis of false diverticula
|
Low fiber diet makes the colon have to develop very high pressures to move food through. These high pressures cause outpouchings of areas that are naturally weaker because they're where blood vessels enter
|
|
What is duodenal atresia?
|
Failure of duodenum to develop
|
|
What other disease is associated wtih duodenal atresia?
|
Down syndrome
|
|
What is the polyhydramnios in duodenal atresia from?
|
Amniotic fluid that has been swallowed and can't go anywhere, causing distension of stomach and duodenum.
Gives rise to double bubble sign on xray |
|
Twisting of bowel around mesentery, leading to ishemia
|
volvulus
|
|
Telescoping of proximal bowel into a distal segment, with resulting infarction causing currant jelly stool
|
intussusception
|
|
What must be present for an intussusception to develop?
|
Must have something for the bowel to "catch" on
Children: usually lymphoid hyperplasia Adults: usually tumor |
|
What must be present for an intussusception to develop?
|
Must have something for the bowel to "catch" on
Children: usually lymphoid hyperplasia Adults: usually tumor |
|
T/F the small bowel is highly sensitive to ischemic injury
|
T
|
|
What HLAs is celiac disease associated with?
|
DQ2 and DQ8
|
|
What is the primary pathologic component of gluten?
|
Gliadin
|
|
caseating lymph nodes may be seen in what?
|
tuberculosis of intestine
|
|
What is mycobacterium avium intracellulare?
|
atypical mycobacterial infection which can occur in the later stages of AIDS.
|
|
What is the stain for acid-fast bacteria? How will acid-fast bacteria appear?
|
Ziehl–Neelsen stain; Appear bright pink
|
|
To diagnose amebic colitis, where will you look for the organisms?
|
In histological section, look for the organism in the necrotic base.
|
|
Sloughed mucosa and mucopurulent exudate form a "____" in C. difficile infection.
|
pseudomembrane
|
|
What is the classic look of C. difficile pseudomembranous colitis on histological exam?
|
see "exploding volcano" exudate coming out of surface
|
|
What is microscopic colitis?
|
Refers to colitis that isn't visible on gross specimen, but when biopsied, see inflammatory cells (increased intraepithelial lymphocytes).
Symptoms are watery diarrhea, but when they get colonoscopy, it looks normal. |
|
What is crypt hyperplastic villous atrophy?
|
Seen in celiac disease. THe villi have atrophied, but the bowel is trying to proliferate, results in hyperplasia or crypts. The section of small bowel looks like colon.
|
|
What is crypt hypoplastic villous atrophy?
|
Seen in radiation enteritis. The bowel has lost ability to proliferate.
|
|
Celiac disease is a ___ cell mediated chronic inflammatory reaction
|
T
|
|
Celiac disease is found almost exclusively in what ethnic group?
|
Caucasians
|
|
What cancer are Celiac patients susceptible to if the disease is refractory?
|
T cell lymphoma (most lymphomas are Bcell).
|
|
What is tropical sprue?
|
damage to small bowel villi due to organism. Responds to antibiotics.
|
|
Where are these primarily found in small intestine?
1) Celiac disease 2) Tropical sprue |
1) Duodenum
2) Jejunum, Ileum |
|
What is Whipple's disease?
|
Systemic infection by gram positive bacillus Trophyerma whippelli.
Macrophages engulf the bacteria but they don't die. The bacterial-laden macrophages then obstruct intestinal lacteals causing impaired transport. |
|
Sx of Whipple's disease
|
Steatorrhea due to obstruction of fat transport
|
|
What stain is used to dx Whipple's disease?
|
PAS - will see it within macrophages.
|
|
What is abetalipoproteinemia?
|
Defeciency in certain lipoproteins involved in making chylomicrons and VLDL.
Deficiency in fat soluble vitamins (A,D,E,K) |
|
Sx of abetalipoproteinemia
|
Steatorrhea
Failure to thrive Vitamin deficiency (esp vitamin E) and its sequelae |
|
What is the wall involvement in
A) Ulcerative colitis B) Crohn's disease |
A) ulceration/inflammation limited to mucosa
B) full thickness inflammation with knife fissures |
|
What is the intestinal location in
A) Ulcerative colitis B) Crohn's disease |
A) Starts in rectum and spreads proximally, always involving continuously (doesn't jump from section to section)
B) Anywhere from mouth-anus, but terminal ileum is most common site. Least common site is rectum. |
|
IBD of the rectum is most likely to be
|
Ulcerative colitis
|
|
Symptoms of
A) Ulcerative colitis B) Crohn's disease |
A) LLQ pain, bloody diarrhea
B) RLQ pain, nonbloody diarrhea |
|
Histology of
A) Ulcerative colitis B) Crohn's disease |
A) Crypt abscesses: see neutrophils in the crypts
B) See lymphs and GRANULOMAS |
|
Granulomas are associated with:
A) Ulcerative colitis B) Crohn's disease |
B
|
|
Gross appearance of
A) Ulcerative colitis B) Crohn's disease |
A) Pseudopolpyps: bumps on colon and loss of haustra
B) Cobblestone mucosa, stricture, thickening, creeping fat |
|
What is the difference in wall thickness in
A) Ulcerative colitis B) Crohn's disease |
A) Normal in thickness
B) Very thickened |
|
What is an aphthous ulcer?
|
Canker sore. Can occur in intestine, common with Crohn's
|
|
Fissures and fistulae are more common with
A) Ulcerative colitis B) Crohn's disease |
B
|
|
Any benign lesion that protrudes above surface of surrounding mucosa
|
polyp
|
|
Benign proliferation of smooth muscle
|
rectal leiomyoma
|
|
What is a hyperplastic polyp?
|
Failure of sloughing. A non-dysplastic lesion. Not necessarily concerning for cancer but a preponderance of them increases risk.
|
|
Sessile serrated adenoma: defn
|
Dysplastic, precancerous lesion in colon.
Unlike traditional colonic adenomas (e.g. tubular adenoma, villous adenoma), they do not (typically) have nuclear changes (nuclear hyperchromatism, nuclear crowding, elliptical/cigar-shaped nuclei). |
|
What gene is frequently mutated in colon cancer, originally leading to a proliferative state, and leading to cancer with DNA hypomethylation?
|
APC
|
|
Pedunculated tubular adenoma: defn
|
The type that leads to cancer.
|
|
What is familial adenomatous polyposis?
|
an inherited condition in which numerous polyps form mainly in the epithelium of the large intestine. While these polyps start out benign, malignant transformation into colon cancer occurs when not treated.
|
|
Treatment of familial adenomatous polyposis
|
Most individuals with the APC mutation will develop colon cancer by the age of 40. Therefore, prophylactic surgery is generally recommended before the age of 25.
|
|
Exophytic: defn
|
Growing outward.
|
|
Annular: defn
|
Growing inward, forming a stricture
|
|
Exophytic carcinomas tend to be ___ sided while annular carcinomas tend to be ____ sided
|
R; L
|
|
Hereditary Nonpolyposis Colon Cancer Syndrome is characterized by mutations in ______ pathway.
|
Mismatch repair.
|
|
What is the carcinoid syndrome?
|
Paroxysmal flushing - vasomotor disturbances
Diarrhea - hypersecretion/hypermotility Wheezing - bronchoconstriction Tricuspid/pulmonary stenosis - endocardial fibrosis |
|
What does it mean when the carcinoid syndrome appears?
|
The tumor has already metastasized to the liver.
|
|
What do carcinoid tumors stain positive for?
|
Chromogranin
|
|
_____ is excreted in urine in patients with carcinoid syndrome
|
5-HIAA
|