Melanoma Flashcards

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1
Q

Phenotypic indications for increased rx melanomA

A
  1. light complexion and inability to tan
  2. red hair
  3. number of atypical nevi greatest than or equal to 10
  4. anatomic location of atypical nevi (especially back)
  5. freckles
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2
Q

FAMMM

A

Familial Atypical Mole and Melanoma Syndrome

1) AKA dysplastic nevus syndrome, atypical mole syndrome
2. characterized by appearance of a large number of dysplastic nevi or atypical moles at an early age in combo with MM

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3
Q

Genet assoc. with MM

A

CDKN2A

-two potential isoforms

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4
Q

CDKN2A

A

1) two potential isoforms

2) trascnribes INK4A and p14ARF

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5
Q

INK4A

A

controls progression through G1-S transition of cell cycle

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6
Q

ARf

A

stabilizes tumor supressor protein p53

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7
Q

other genes involved in MM

A
  1. CDK4

2. MC1R

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8
Q

CDK4

A

also involved in g1-s transition

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9
Q

MC1R

A

melanocortin 1 receptor

  • found on surface of melanocytes
  • red hair and freckles assoc with certain alleles of mc1r
  • phenotype is assoc. with increased rx MM
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10
Q

pertinent family hx predicators

A

1) MM in first- or second-degree relatives
2) MM of more than three occurrences among any family members
3) MM with multiple primaries in one parent
4) MM with multiple primaries in any one individual
5) MM with multiple cases on same side of family
6) MM diagnosed in family member at young age (before 30)
7) Pancreatic adenocarcinoma
8) Breast cancer
9) Central nervous system cancers
10) Non-melanoma skin cancer

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11
Q

dx melanoma

A
  1. requires dermatological/provider investigation
  2. ABCDES
  3. asymmetry, itch, bleeding, satellite moles, moles growing in pattern around existing moles
  4. bx to stage
    - wide local excision
    - lymph node mapping
    - imaging studies
    - lab assay (LDH)
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12
Q

familial patters

A
  1. younger at time dx < 30
  2. more affected in 1st or 2nd degree releatives
  3. higher risk for subsequent primary tumors
  4. poor ability to tan, fair skin, red hair, multiple melanocytic nevi
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13
Q

sporadic patterns

A
  1. older at time dx > 30
  2. no affected 1st/2nd degree relatives
  3. few or no subsequent primary tumors
  4. less likely to have poor ability to tan, fair skin, red hair
  5. few or no dysplastic nevi
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14
Q

Stage I mgmnt

A

surgical removal lesion with free margin

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15
Q

stage II

A

surgical wide excision +/- sentinel node biopsy

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16
Q

stage III

A
  1. wide excision
  2. node bx
  3. adjuvant therapy with interferon
17
Q

stage IV

A

poor prognosis

-mets present
-surgery to debulk tumor
and prodive symptomatic relief
-rediation
-chemo
-no improvement overall survival