Colorectal Flashcards
MC cause of death after TAC in FAP
How to prevent
duodenal adenomas and adenocarcinoma.
Prevention includes regular upper esophagogastroduodenoscopy every 2 to 3 years @ 20-25 YO
How to monitor anal tissue after TAC in FAP?
Regular procto with Bx
surveillance after TAC with IPAA in FAP?
q1 year vs q2 (elevated risk for rectal recurrence)
score says q1yr endoscopy
when to perfrom an IPAA after proctocolectomy
6 mos at least.. still need a DLI x 6-8 wks fr IPAA to heal
FAP surveillance?
Flex proctosigmoidoscopy @10 to 12 years (repeated every 1-2 years until age 35 and every 3 years thereafter)
Upper endoscopy every 1 to 3 years once polyps are identified
Cowden disease surveillance?
PTEN mutation (hamartoma dz)
Clinical thyroid examination (annually)
Mammography annually beginning at age 30 or 5 years before earliest breast cancer diagnosis in family members
Routine colonoscopic surveillance
Peutz Jeghers syndrome surveillance
HAMARTOMAS
Upper endoscopy
Small bowel radiographic study
Colonoscopy (every 2 years)
Pancreatic ultrasound (annually)
Gynecologic examination with pelvic ultrasound
Mammography annually (beginning at age 25)
CDH1 mutation (e-cadherin)
hereditary diffuse gastric cancer and increased risk for breast ca
when to ppx gastrectomy in hereditary diffuse gastric ca?
20-30 YO
Lynch syndrome = hereditary nonpolyposis colorectal ca
ADominant. DNA mismatch repair = MLH1, PMS2, MSH2, and MSH6.
A deletion in the epithelial cell adhesion molecule, which results in MSH2 promotor methylation, can also cause HNPCC.
how to dx HNPCC
AMSTERDAM CRITERIA.
3+ family members with CRC (1 first degree)
2+ generations
1 <50 YO
what kind of cancers pop up in HNPCC?
RIGHT sided colon cancer
Endometrial tumors
Ovarian tumors
Stomach ca
Urinary tract ca
Small bowel ca
CNS ca
APC somatic vs germline mutations
somatic: in more than 80% of sporadic colon cancers
germline: cause familial adenomatous polyposis (FAP).. TSG regulates intracytoplasmic B-catenin
HNPCC screening?
Colonoscopy at age 20 to 25 years (repeated every 1-3 years)
Transvaginal ultrasound or endometrial aspiration (females) at age 20 to 25 years (repeated every year)
colorectal met chemotherapy
bevacizumab, fluorouracil, and oxaliplatin/irinotecan
or FOLFOX (leukovorin, fluoro, oxali)
early stage rectal ca transanal excision margin
1cm; full thickness
rectal ca staging ERUS vs MRI
MRI is much better at detecting mesorectal fascial involvement for CRM (CIRCUMFERENTIAL MARGIN = important PROGNOSTIC indicator)
colon ca postop chemo indication
node positive or M1 AKA… .STAGE III AND ABOVE.
FOLFOX 6 mos (or 3/3)
primary peritoneal mesothelioma
2/2 asbestos
50+ YO
M>F
staging of primary peritoneal mesothelioma
The T-stage based on peritoneal cancer index (PCI) - size and distribution of the tumor
T1 is a PCI score of 1-10
T2 is a PCI score of 11-20
T3 is a PCI score of 21-30
T4 is a PCI score of 31-39.
T1N0M0 disease is classified as stage I disease
T2-3N0M0 is classified as stage II disease
stage III disease is any T4 disease, or any T1 or greater disease with the presence of node-positive or metastatic disease
mgmt primary peritoneal mesothelioma
HIPEC / CRS
pseudomyxoma peritonei mgmt
CRS HIPEC - does not travel lymphatically so can just do an appendectomy and not a R hemi
2.5mm nodules all removed; if cannot get <2.5mm, don’t do HIPEC (no survival benefit)…
NOT radiosensitive.
rectal carcinoid tumor mgmt
Transanal excision is adequate for tumors less than 2 cm in diameter
Proctectomy would be indicated with mesorectal excision for larger lesions (> 2 cm).
Invasion of the muscularis propria (T2) has been associated with lymph node metastases in up to 47% of patients.
Systemic chemotherapy is used in metastatic carcinoid lesions; however, its efficacy is limited
colon carcinoid mgmt
<1cm polypectomy
>1cm formal resection
Postop surveillance after oncologic colon cancer resection?
CEA every 3 to 6 months
CT chest/abdomen/pelvis every 6 to 12 months
Colonoscopy at 12 months
indications for proctocolectomy with or without IPAA in ULCERATIVE COLITIS
colorectal cancer, a non–adenoma-like dysplasia-associated lesion or mass (DALM), or high-grade dysplasia
which sx get better after colectomy in UC?
anemia, uveitis, arthritis, episcleritis improve
50% pyoderma gangrenosum, erythema nodosum
which sx do not get better after colectomy in UC?
PSC and ankylosing spondylitis
how long should an ileal J pouch be?
15-20 cm
what mutation associated with IBD
NOD2, HLA B27
pelvic floor dysfunction causing constipation
dx and mgmt
Sitzmarker study (distal accumulation) combined with an abnormal defecography or functional MRI
physical therapy and biofeedback training to retrain the pelvic floor muscles to relax properly to allow for normal defecation.
mgmt of toxic megacolon in UC
total colectomy without proctectomy (damage control) with end ileostomy
(can trial medicien first (NGT, fluds, steroid, bowel rest, CTX/Flagyl))
UC presentation
bloody diarrhea, pain, weight loss (less than Crohns)
UC dx
path colonoscopy = pseudopolyps, collar button ulcer, crypt abscesses, anal sparing
UC screening
8 years after dx, every 1-2 years
All abnormal lesions must be biopsied along with random biopsies performed in 4 quadrants every 10 cm along the colon and rectum
Crohns screening
8 yrs after dx q1yr
Surveillance should be performed using either random biopsies or chromoendoscopy every 1 to 3 years or more frequently if mandated by findings
MC site of perforation UC vs Crohns
transverse colon vs distal ieum
2cm+ mass on appendectomy
hemi
MC extraintestinal manifestation of UC requiring colectomy
FTT
mgmt of colovesical fistula with fecaluria presentation
- abx
- let all inflammation subside
- colectomy with fistula takedown, bladder closure, omentum interposition between colon and bladder
Gardner (desmoids and polyposis) encounter mesenteric desmoid during colectomy
core bx it; don’t resect (will end up resecting more than you should… short gut)
Crohn’s disease pathology on Bx
transmural involvement, segmental disease (skip lesions), cobblestoning, narrow ulcers, creeping at, GRANULOMAS
mgmt of Crohn’s maintenance
sulfasalazine, loperamide
refractory: remicade/infliximab (TNF-a inhibitor) good for fistulas
mgmt of Crohn’s acute
steroids
surgery in Crohn’s
NOT curative (unlike UC)… no LIS for fissure, no takedown of fistulas I.e.
rly only indication:
blind loop obstruction
anorectal advancement flap vs colostomy in anorectovaginal fistulas
strictures (see other card)
if resecting in Crohn’s, margins?
2 cm away from gross disease
severe colonic disease in Crohn’s necessitating surgery
proctocolectomy and ileostomy is procedure of choice
NO POUCHES/IPAA In CROHNS
incidental Crohn’s disease when suspected appy
take out appy (will confound in future)
stricture disease in Crohn’s
MC is resection if SHORT ISOLATED SEGMENT
consider stricturoplasty if impending short gut
<10cm: (longitudal incision close transversely = Heineke-Mikulicz)
10-20cm: FINNEY (fold stricture segment and make common channel
>20cm: MICHELASSI: same as finney but longer
Make sure to Bx if stricturoplastying
CI to stricturoplasty: malnutrition, presence of inflammatuion/fistula, malignancy
MC complication after stricturoplasty?
bleeding! not perf/restricture interestingly
;.;;oxalate stones in Crohn’s s/p TI resection
decrease oxalate binding to Ca 2/2 increased intraluminal fat
oxalate goes into colon
released in urine
ca-oxalate kidney stones
Rectal prolapse management
high fiber diet
if old/sick: Altemeier = perineal rectosigmoid resection transanally - HIGHER RECURRENCE, LESS DURABLE
if can tolerate: transabdominal rectopexy (open vs lap) +/- LAR or sigmoidectomy if CONSTIPATION concurrent.
What is positive node
0.2 mm of cancer deposit
circular layer of muscle in colon?
muscularis PROPRIA
what is haustra?
transverse bands made up of plicae semilunares