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41 Cards in this Set

  • Front
  • Back
what is congenital aganglionosis
hirschsprungs disease- absence or PS neuronal cell bodies of enteric ganglia
What is genetic disorder is common in Hirschsprungs
trisomy 21
the myenteric plexus is also named?
auerbachs
The genetic problem resulting in hirschprungs is commonly due to what?
RET gene loss of function...TK receptor, plays a role in neural crest development
What is the most common congentil cause of intestinal obstruction?
Hirschsprungs
How is DX made for hirschsprungs?
suction rectal biopsy- you see absence of submucosal enteric ganglion cells and hypertrophy of non-enteric PS nerves that innervate the enteric ganglion
What is the most common functional GI tract disorder?
Irritable bowel syndrome
What are the DX criteria for IBS?
absence of structural abnormalities, ROME III criteria, and must rule out alarming sx, like anema, FOB, weight loss
What is diverticulosis?
acquired herniations of mucosa/submucosa into muscularis propia (externa)
The muscular wall around pseudodiverticula in diverticulosis looks like what?
hypertrophied
What is the pathogenesis of diverticulosis?
prolonged increased intraluminal pressure

lack of adequate fiber
Diverticular disease most often effects what part of the colon?
Sigmoid colon
What is diverticulitis?
Inflammation destroys and weakens the wall forming an abcess and then perforation. Fistulas form between adjacent structues.
Can diverticulitis have a positive fetal occult blood test?
Yes
Clostridium difficile in pseudomembranous colitis is found in what two instances?
neonatal enterocolitis NEC

or older adults following antibiotic therapy
What is pathognomonic for Crohns diseases?
noncaseating granulomas with multinucleated giant cells
If you see crypt abcesses, what are they more common in UC or CD?
ulcerative colitis
In radiography, what does the string sign point to?
Crohns disease
Buzz-word: cobblestonign
Crohns
Buzz-word: creeping fat
Crohns
CD effects what portion of the gut wall?
Transmural or full thickness
Where do you see Paneth cell metaplasia in the left colon?
Crohns
Where do you see apthous ulcers?
Crohns
In UC vs CD, what has continuous lesions?
Ulcerative colitis
In radiography, a "lead pipe" appearance, points to?
Ulcerative Colitis
If you fail to see any colonic haustra, you should be thinking?
Ulcerative colitis
inflammatory pseuopolyps can be found in?
UC
The clinical presentation of CD vs UC
CD: RLQ colicky pain, aphthous ulcers

UC: left sides bloody diarrhea with mucus
p-ANCA positive, and ASCA negative, makes you think?
Ulcerative Colitis
Hamartomatous polyps are abnormal proliferations of?
normal tissue constituents
Cowden's syndrome is autosomal?
dominant
Peutz-Jeghers polyposis is autosomal?
dominant
Mucosal pigmentation, like blue lips, is seen in?
Peutz-Jeghers polyposis
What is a greater risk for adenocarcinoma, tubular or villous adenomas?
Villous
Familial adenomatous polyposis usually involves what gene?
APC, inactivation of it, it's a tumor suppressor gene
Gardner's syndrome is of what inheritance?
autosomal domintnat
Turcot's syndrome is of what inheritance?
autosomal recessive
FAP is of what inheritance?
Autosomal dominant
If you see polyposis with desmoid tumors and osteomas, you should be thinking?
Gardner's syndrome
What is the adenocarcinoma or vogelgram sequence?
APC----RAS-----p53
The second most common cause of colorectal cancer is ____and what are the two common ones of that?
DNA mismatch repair gene

two most common are MLH1, MSH2