Polyps Flashcards

1
Q

Polyps classification:

A
  1. Hamartomatous
  2. Adenomatous
  3. Inflammatory
  4. Mixed polyposis syndrome
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2
Q

Eg of hamartomatous polyps

A
  1. Solitary Juvenile polyp
  2. juvenile polyposis dyndrome
  3. Peutz-Jeghers syndrome
  4. Phosphatase and tensin homolog gene mutation (PTEN)
    a. Bannayan-Riley-Ruvalcaba syndrome
    b. Gorlin syndrome
    c. cowden syndrome
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3
Q

Eg of adenomatous polyps

A
  1. Familial adenomatous syndrome
  2. Turcot syndrome
  3. Gardner syndrome
  4. Lynch syndrome
  5. MYH-associated polyposis
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4
Q

Solitary Juvenile polyp

A

painless rectal bleed
<5 in number
mean age 4, (2-6)
often rectosigmoid area
histo: dilated cysts filled with mucin, abundant lamina propria and inflammatory cells

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5
Q

Juvenile polyposis dyndrome

A

> 5 polyps
genes: SMAD4, BMPR1A. ENG1

Risk of Ca: 68% by age of 60 yo

screen: all family members should be tested for the mutation

EGD/CS: at 10-15 yo e 2-3 yr
if polyp present, yearly until no polyps
then back to e 2-3 yr

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6
Q

Peutz-Jeghers syndrome

A

AD, genes: STK11 (LKB1)

Dx:
1. 2 polyps with histology PJS
2. Any number polyp + family with PSJ
3. Mucocutanous pig. + family with PSJ
4. Any number polyp + mucocutanous pig.

Ca risk: colon, lungs, testes, breast, uterus, ovaries

Surveillance:
EGD/CS at 8 yo
if polyps seen –> e 3 yr
if no polyps –> start at 18 then e 3 yr
VCE at 8 yo then e 3 yr

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7
Q

Familial adenomatous syndrome

A

AD, APC gene
EIM:
bone- osetomas, sclerosis
dental-unerupted, supernumery
connective tissue-desmoid tumor
eye-CHRPE
Ca-hepatoblastoma, thyroid, adenal and glioblastoma

Dx:
1. FHx + neg gene–> no f/u
2. FHx + known genotype –> at 10-14yo sigmoidoscopy e yr + CS e 5 yr
3. FH + unknown genotype –> at 10-14yosigmoidoscopy e yr + CS e 5 yr until rectal adenomas found. Then yearly EGD/CS

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8
Q

Medical options for FAP

A
  1. Sunlindac
  2. NSAIDS
  3. Vit C
    DNT replace surgery
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9
Q

Polyps removal

A

5mm: biopsy forceps
>5mm: snare electrocautery
>2cm: piecemeal removal

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