Wk 7 Melanoma Flashcards

1
Q

Stages of melanoma

A

Stage 0: confined to epidermis
Stage 1: localized

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2
Q

What is Breslow depth?

A

Measurement in mm of depth of melanoma for staging

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3
Q

Melanoma growth patterns

A

Nodular -> greater mortality

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4
Q

What does survival w/ melanoma relate to most?

A

Lesion depth
-increased depth by mm -> higher T stage

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5
Q

Warning signs of melanoma acronym

A

Asymmetry
Border (irregular)
Color (multiple)
Diameter (>6 mm)
Evolving

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6
Q

Melanoma characteristics in darker skin types

A
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7
Q

What is ALM?

A

Acral lentiginous melanoma

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7
Q

Where does ALM appear most often on darker skin?

A

feet, nail beds, palms
-most common melanoma subtype

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8
Q

What are melanocytic nevi?

A

=Moles
benign neoplasms of melanocytes
-tend to arise in adolescence, peak by late 40s
-start at junction of epidermis and dermis
-w/ age become elevated, lose pigmentation, eventually regress
-junctional -> compound -> intradermal -> regression

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9
Q

Do nevi give rise to melanoma?

A

increase melanoma risk 2-4 fold
-nevus cells in 25-40% of melanomas
-.50% of melanomas arise de novo

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10
Q

Images of common melanocytic nevi

A
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11
Q

3 types of nevi

A
  1. congenital
  2. blue nevus
  3. halo nevus
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12
Q

Common nevi in darker skin

A
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13
Q

Examples of when to biopsy or not

A

Tricky b/c many have features of benign and malignant

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14
Q

3D melanoma detection

A
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15
Q

What is dermoscopy?

A

=multiple objective scoring system
-increased accuracy for experienced users, decreases for inexperienced
-NOT diagnostic but can increase confidence of dx
-can see deeper and diff structures of skin

16
Q

What are signature lesions?

A

Characteristic patterns in some patients’ nevi
-does a given atypical lesion fit into a characteristic pattern?
-look for the ugly duckling lesion - the one that doesn’t fit with others= suspicious

17
Q

What is seborrheic keratosis?

A

ABCD not sufficient
-warning sign of melanoma, but not melanoma

18
Q

Compare evolving nevi and melanoma

A

Nevus - gradual change (no change month-to-month)
-maintains shape and pigment distribution, uniform darkening or lightening, uniform regression

Melanoma - rapid enlargement (>3 mm^2/ year), changes shape and pigment distribution, non-uniform darkening or lightening and regression

19
Q

What is greatest increased risk for melanoma?

A

Family Hx (10-30x), approx 10% of melanoma patients
~33% of melanoma-prone families have germline variants in CDKN2A

20
Q

What is the only way to document changes in nevi or melanoma?

A

Photography

-disadvantage - only monitoring known lesions

-most lesions de novo, so might miss new ones

21
Q

What is the only way to document changes in nevi or melanoma?

A

Photography

-disadvantage - only monitoring known lesions

-most lesions de novo, so might miss new ones

22
Q

What is diagnostic 2-GEP?

A

=Pigmented lesion assay
-tape-stripping
-collect cellular RNA from adhesive patch over lesions followed by quantitative PCR

-a 2 gene screening test for LINC00518 and PRAME
-both -> high risk (>90%)
-only one gene =moderate (10-50%)
-neither gene = low risk (1%)

23
Q

Primary melanoma tx

A

Excision
-margins based on tumor depth

24
Primary melanoma tx
Excision -margins based on tumor depth
25
How does immunotherapy work?
-utilize checkpoint inhibitors, which provide a negative signal to T cell so that it won't kill a cell -therapy provides a negative signal to the negative signal, allowing the T cell to kil the cell
26
What are the 2 phases of T cell activation?
1. priming phase: anti-CTLA4 2. Effector phase: anti-PD1
26
Driver mutations in melanoma
BRAF is most common (involved in RAS/MAPK pathway)
27
Targeted therapy for melanoma
-inhibits mutant BRAF -resistance very common, side effects -not given as first therapy (give immunotherapy first)
28
What is the best tx option for a patient w/ hx of mutant BRAF+ melanoma who develops distant metastases?
B. Immunotherapy -BRAF inhibitor + MEK inhibitor = too toxic -radiation not very effective for melanoma