large intestine Flashcards

(40 cards)

1
Q
failure of neural crest cell migration
dysfunctional Auerbach (muscularis externa layer) + Meissner plexus (submucosal layer) → abnormal peristaltic waves
A

Hirschsprung disease

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2
Q

congenital megacolon with meconium ileus or if less severe, chronic constipation as infant (chronic distention)

A

Hirschsprung disease

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3
Q

twisting of colon around mesentary → ischemia

A

volvulus

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4
Q

most common location of volvulus in elderly (most commonly affected by volvulus)

A

cecum or sigmoid colon

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5
Q

most abundant bacterial flora in large intestine

A
#1 bacteroides fragilis
#2 E. coli (enterobacteraciae)
other enterobacteraciae:
proteus mirabilis
proteus vulgaris
salmonella
shigella
klebsiella pneumoniae
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6
Q

complication of obstruction of appendicitis with:

adults: fecalith (fecal stone)
kids: viral infection (hyperplasia of lymphoid tissue= MALT tissue)

A

appendicitis

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7
Q

N/V
diffuse periumbilical pain → later, pain localizes to RLQ (McBurney’s point)
rebound tenderness in RLQ
leukocytosis on CBC

A

appendicitis

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8
Q

McBurney’s point

A

2/3 the way from umbilicus to ASIS

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9
Q

confirm diagnosis of appendicitis

A

r/o ectopic pregnancy with female (serum bHCG)
adults: CT scan
kids or pregnant: US

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10
Q

line anus that marks end of endoderm and beginning of ectoderm (squamous cell)

A

pectinate line

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11
Q

pathology proximal to pectinate line

A

internal hemorrhoids: not painful, may bleed

tx: can band → necrosis

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12
Q

sensory + arterial blood supply + venous drainage above and below pectinate line

A

above: no sensation, superior rectal artery (from IMA), superior rectal vein (to IMV)
below: sensation, inferior rectal artery (from pudendal artery - not IMA), inferior rectal vein (to internal pudendal vein → to internal illiac vein→to IVC)

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13
Q

cancer above pectinate line is most likely

A

adenocarcinoma (rectal)

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14
Q

pathology distal to pectinate line

A

external hemorrhoids: very painful

tx: numbing agent -symptomatic relief

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15
Q

cancer below pectinate line is most likely

A

squamous cell carcinoma (anus)

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16
Q

biggest risk factor for squamous cell carcinoma of anus

A

HPV 16, 18, 31

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17
Q

inflammation of perianal region + rectum due to fecal matter in area for an extended period of time
associated with ulcerative colitis
tx: topical steroids

18
Q

most common type of polyp in colon - found in rectum or rectosigmoid

A

hyperplastic polyp

19
Q

polyp with no precancerous risk (benign)

removed during colonoscopy since need bx to prove not cancerous

A

hyperplastic polyp

20
Q

types of adenomatous polyp (neoplastic - precancerous polyp for adenocarcinoma)

A
tubular adenomas (lots of glands)
tubulovillous adenomas
villous adenomas (most VILLainOUS - most precancerous, lots of finger-like projections)
21
Q

child

A

juvenile polyps
if one: no malignant potential
if many: juvenile polyposis syndrome →↑ risk adenocarcinoma

22
Q

AD
multiple benign hamartomas in GI tract (excess accumulation of normal tissue that is located at the site of growth)
hyperpigmentation: lips, mouth, hands, genitalia
↑ risk cancer (50% by 60 yo): colorectal cancer, small intestinal, stomach, pancreatic, breast, ovarian, uterine

A

Peutz-Jeghers Syndrome

23
Q

risk factors for colon cancer

A

IBD: UC > chron’s
smoking
high fat/low fiber diet
alocohol use
obesity
adenomatous polyps (villous adenomatous polyps greatest risk)
strep bovis bacteremia: 50% of colon cancer patients colonized it in their stool
polyposis syndrome: FAP, HNPCC, Peutz-Jeghers syndrome, juvenile polyposis

24
Q

fatigue, weight loss, LAD, night sweats
abdominal pain, bowel obstruction → N/V
change in bowel habits if L-sided colon affected: “pencil-thin stools”
hematochezia: if rectosigmoid region affected
IDA - chronic GI bleed: if R-sided colon

25
incidental finding of anemia in >50 yo
screen for colon cancer (GI bleed - most commonly R. sided cancer)
26
diagnosis of colon cancer
``` colonoscopy: >50 yo fecal occult blood testing barium enema flexible sigmoidoscopy confirmation: tissue bx ```
27
"apple-core" lesion with barium enema
narrowing of lumen of colon | suggest colon cancer
28
CEA is a tumor marker for
colon cancer | nonspecific: but useful for monitoring for recurrence after treatment for colon cancer
29
AD (germline) mutation in APC gene 1000s of polyps begin at young age 100% progress to colorectal cancer unless colon is resected
familial adenomatous polyposis (FAP)
30
FAP (mutation of APC gene, 1000s of polyps) + malignant CNS tumors (medulloblastoma)
turcot syndrome TURcot = TURban (brain tumors)
31
FAP (mutation of APC gene, 1000s of polyps) + bone and soft tissue tumors (lipomas, retinal hyperplasia)
Gardner syndrome lumpy vegetables in garden = lumps, bumps all over body
32
AD mutation in DNA mismatch repair gene → microsatelite instability pathway colorectal cancer DOESN'T arise from polyp (nonpolyposis colorectal cancer) PROXIMAL colon cancer (vs 50% of colon cancer in distal 1/3 -distal to splenic flexure)
Heriditary nonpolyposis colorectal cancer (HNPCC/Lynch syndrome)
33
>60 yo with many blind pouches in sigmoid colon usually asymptomatic or vague pain in LLQ RELIEVED with defecation or painless rectal bleeding
diverticulosis
34
true diverticula
outpouching of all three layers of gut wall | example: meckel diverticulum
35
false diverticula
outpouching of only mucosa + submucosa due to weak spots in muscularis externa (where vasa recta perforate muscularis externa) example: colonic diverticulum
36
diagnosis
barium enema
37
``` LLQ pain (sigmoid colon) fever elevated WBC count rectal bleeding constipation due to inflammation in colon peritonitis (if perforation) ```
diverticulitis
38
free air in abdomen (below diaphragm) on CT scan
perforated bowel from: appendix PUD diverticulitis
39
treatment of acute flare of diverticulitis
antibiotics: metronidazole (anaerobic bacteria) + TMP-SMX or FQ (ciprofloxacin)
40
screening colonoscopy guidelines
begin at 50 yo if + family history: begin at 40 yo or 10 yr before youngest 1st degree relative diagnosis if FAP: every year from 10-12 yr to 35-40 yr if Lynch syndrome: begin at 20-25 yo or 10 yr before youngest relative diagnosis