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54 Cards in this Set

  • Front
  • Back
atresia
absence of nL opening or failure of tubular structure
stenosis
narrowing of lumen
diverticula
- jejunum, ilium
- in mesenteric border at sites of penetration of blood vessels
why is there bacT overgrowth in diverticula?
overgrowth in content "stasis" b/c content doesn't move around
other things that happen w/ diverticula?
stenosis
ulcer
bleeding
Meckel diverticulum
- ileum
- persistent vitelline duct
- 1-3 ft?? from ileocecal valve
what abnL tissue may be present in meckel diverticulum?
heterotropic gastric mucosa
heterotrophic pancreatic tissue**
abnL in size
may be mistaken for a TUMOR
malabsorption syndromes
- whatever you need is not absorbed and it is excreted out
what happens w/ excretion in malabsorption syndrome?**
steatorrhea - bulky, greasy, foul smelling feces
--> fat, vitamins, mineral, carbohydrates, proteins
what defects cause malabsorption?

MCC in US?**
digestion, absorption, transport

- Celiac ds and Crohn's ds
specific abnLs that cause malabsorption?"
Crohns
Whipple
Lymphoma
TB
Diverticulosis
Blind loop syndrome
clinical features of malabsorption
steatorrhea
weight change, abd distention
skeletal changes
dermatitis, peripheral neuro
excessive diarrhea
celiac ds
- villous atrophy of jejunal mucosa
- improvement w/ w/d of gluten containing food
patho of celiac ds
- immune rxn to gliadin
- T cell mediated
- gluten -> ab -> t cell -> t cells + ab react to cells -> destruction -> villous atrophy
celiac ds:
genetic predisposition
MCC of...**
complications
- clustering HLA-B8, DQ2
- flat biopsy
- MC - lymphoma
tropical sprue
- MC in 3rd world
- enterotoxigenic E. coli
- possible villous atrophy
- folate/B12 def common
Whipple ds
- multi-system***
- M:F 10:1; 40-50
-***foamy macro w/ granules in villi
- *tropheryma hippelii - gram + actinomycete; PAS stain
what 3 things is whipple ds a/w?
1. lactase deficiency
2. bacT overgrowth
3. abetalipoproteinemia
lactase def
- seen in whipple ds
- diarrhea & malabsorp
- common in black americans
bacT overgrowth
- seen in whipple ds
- abnL large pop of bacT in jejunum
- due to lumenal stasis
- a/w hypochlorihydria & achlorhydria
abetalipoproteinemia
- familial, inborn error
- (-) lipoprotein transport
- lipid vacuolation of mucosal cells
- failure to absorb essential FA
MCC causes of obstruction**

what % of cause?
1. hernia
2. adhesions
3. intussusception
4. volvulus

80%
how are intestinal obstructions mostly acquired?
surgery
hernia
usually in inguinal canal; femoral canal; umbilicus; sx scar; defect in post wall
- incarceration -> obstruction
- pressure -> venous -> arterial -> strangulation -> gangrene
adhesions
- after peritonitis or hx of operations
- congenital fibrous bands from Meckel diverticulum
intussusception**
- invag of proximal intestine to distal
- drags mesentery and vessels --> strangulation --> infarction
- MC in children
- adults: tumor mass is leading
volvulus
twisting of loop of bowel
in SI or sigmoid colon
Ischemic bowel ds:
- cause
- acute
- chronic
- dec blood flow to SI
- MCC of occlusive ischemic BD-> mucosal necrosis ->transmural infarction
- less common, atherosclerosis
A.I.I.:
MCC
other causes
SMA occlusion
- thrombosis, embolism
- nonocclusive ischemia - hypoperfusion
- hypotension
- ischemia ->necrosis -> infarction
AII:
mesenteric venous thrombosis
- portal venous thrombosis
-**pylephlebitis -> inflamm of portal vein
AII:
secondary to
morphology
micro
- intestinal obstruction
- dusky, purple-red, moist, easily torn
- inflamm along margin of infarct; perforation risk high for 3 d
nonocclusive hypoperfusion
only mucosal infarction; corrected w/ inc blood flow and totally reversible
acute abd
- abrupt onset pain
- anginia
- perforation and shock common
Chronic intestinal ischemia
atherosclerosis
recurrent pain - celiac compression syndrome
IBD
1. infectious ds
2. noninfectious conditions
3. idiopathic IBD
how is idiopathic IBD dx'd?
dx of exclusion: exclude infectious and noninfectious conditions
epidemiology of IBD
- freq in US, Britian, Scandinavia
- increase incidence in US
- common in 20-30s
- white 5x more susceptible
- UC > CD
CD and UC
10-20% can't be differentiated --> indeterminate colitis
CD
- mouth -> anus; MC in terminal ileum
- **discontinuous lesions
CD:
morphology**
skip areas
creeping fat
wall thickening w/ inflamm
string sign
string sign
narrowing of gut lumen, w/ mucosal edema, ulceration and sloughing --> fibrous strictures
CD extra intestinal manifestations
pericholangitis
amylodidosis
stomatis
arthritis
iritis
CD MC site
UC MC site
- terminal ileus (regional ileitis) and colon (Granulomatous Colitis)
- colon and rectum
UC:
sites
morphology**
- colon & rectum; continuous lesions
- rectum -> colon
- backwash ileitis
- proctitis (confined to rectum)
- pancolitis (up to R colon)
UC:
backwash ileitis
- UC that involves terminal ileum (10%)
UC:
clinical
complications
-bloody d
- severe chronic ulceration -> colonic dilatation-> systemic toxicity -> toxic megacolon***

- development to carcinoma in 1% in 10 yrs; >30% in 30 yrs
CD vs. UC ddx
CD: **fistula, **skip lesions, **transmural inflamm (fissures/granulomas), **fibrous strictures
UC: **rare fistulas, **cont. lesions, **submucosal inflamm, **strictures rare
rat tailing effect
skip areas --> wall thickening w/ nL segments in between
results in areas of narrow and nL areas
tumors in SI:
benign
- rare
- **Peutz-Jeghers syndrome - hereditary GI polyposis a/w excessive melanin pig.
tumors in SI:
malignant
- carcinoid, lymphoma, adenocarcinoma
Carcinoid tumor
* NE tumor
- from NE cells of GIT mucosa; *low malignancy
- **can give you carcinoid syndrome
- locally invasive, ICS (ileum, colon, stomach)
- freq metastasize
carcinoid syndrome:
general

symptoms
- R heart then lungs
- not L heart b/c of monoimunoxidase destruction of serotonin

-> flush, bronchoconst, inc urine 5-HIAA
serotonin in carcinoid syndrome
send urine to lab --> serotonin decarboxylated in liver to 5-HIAA and excreted in urine**