Basal Cell Nevus Syndrome - PowerPoint PPT Presentation

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Basal Cell Nevus Syndrome

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DESIGN: Prospective, randomized study. SETTING: University dermatology departments ... Primary end point was clinically assessed lesion clearance at 3 months ... – PowerPoint PPT presentation

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Title: Basal Cell Nevus Syndrome


1
Basal Cell Nevus Syndrome
  • Daniel Berg M.D., FRCPC
  • Director, Dermatologic Surgery
  • University of Washington

2
Thank Goodness.. Shade at Last!
3
Basal Cell Nevus Syndrome
  • Autosomal Dominant
  • 50 risk of passing on
  • In the skin
  • Numerous Basal Cell Carcinomas
  • Beginning at young age
  • Sensitivity to Radiation Treatment
  • Palmar Pits

4
BASAL CELL CARCINOMA (BCC)
  • Commonest Cancer U.S. 800,000/yr
  • 99 in Caucasians
  • 95 between age 40-79
  • 85 on Head Neck
  • Risk of Metastasis Very Very Low
  • Main potential problem Local Invasion

5
EPIDEMIOLOGY
  • LIFETIME RISK OF BCC AND SCC
  • MEN 18.6
  • WOMEN 18
  • (based on B.C. data - lifespan 75 yrs.)

6
BCNS Time of Onset BCC
  • Before puberty 15
  • By age 22 50
  • By age 35 90
  • None over age 30 10

7
Remember this?
  • DNA molecules make up genes
  • Genes are blueprints for Proteins
  • Proteins are the building blocks of body
    functions
  • Some proteins control cell growth

P
M
D
  • Everyone has two copies of each gene
  • One each from Mum and Dad

8
Tumor Suppressors Proteins that normally act as
brake on cell growth.
P
Patched
Smo
Inhibits
Downstream Target Genes
Growth
Induces
9
Patched
P
P
Normal Cell
Cell at Risk
BCC Cell
10
UVB
Ultraviolet Light
11
Spring Break - circa 1900
12
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13
BASAL CELL CARCINOMA
  • CLINICAL PRESENTATION
  • Nodular
  • Superficial
  • Morpheaform
  • Pigmented

14
Nodular
15
Superficial
16
Pigmented
17
Morpheaform
18
Infiltrative
19
NonMelanoma Skin Cancer
  • Choice of Treatment
  • Balance
  • CURE RATE
  • FUNCTIONAL RESULT
  • COSMETIC RESULT

20
Choice of Treatment
  • Special Features in BCNS Patients
  • Numerous BCCs expected
  • Save more complicated surgery
  • Early detection more important
  • Size
  • Consequences if recurrence
  • Pathology
  • Patient Concerns

21
Treatments
  • Topical
  • 5FU (Effudex)
  • Superficial only
  • Imiquimod (Aldara)
  • Just approved by FDA 2004
  • Surgery
  • EDC (scrape and burn)
  • Excision
  • Mohs
  • Regular

22
Treatments
  • Radiation
  • Not in BCNS
  • Other
  • PDT

23
ED C (scrape burn)
  • CURE FOR SMALL PRIMARIES gt90
  • ADVANTAGES
  • Inexpensive
  • Outpatient Office Procedure
  • Quick
  • DISADVANTAGES
  • High Recurrence Rate for Difficult Tumors
  • Location, recurrent, deep

24
EDC
Initial Lesion (BCC)
Curettage (after biopsy)
25
EDC
Desiccation
Repeat X 3
26
Final Defect
EDC
Typical Scar
27
SURGICAL EXCISION
  • CURE FOR PRIMARY TUMORS gt 90
  • ADVANTAGES
  • Inexpensive
  • Often office or outpatient procedure
  • DISADVANTAGES
  • More difficult with recurrent, indistinct tumors
  • Margin control difficult in some locations

28
PDT
  • Not approved for BCC in USA
  • Combination of Drug Light Effect
  • Drug can be given as cream, by mouth or iv.
  • Currently two topicals approved in USA (AK)
  • Levulan Kerastick
  • Metvix
  • Some studies in BCC exist
  • Metvix - 70 Cure at 2 years (Arch Derm 2004)

29
PDT
PDT Pathway
PDT Selectivity
30
Topical Imiquimod (Aldara)
  • Approved FDA 2004 for Superficial BCC
  • 5 nights per week
  • Total 6 week course
  • Cure 70-85
  • Not tested in lesions lt1cm from eyes, nose,
    mouth, ears
  • Largest diameter 2cm
  • Side Effects
  • Significant irritation at site common

31
Topical Imiquimod
  • Possible role in nodular BCC
  • Cure Rates 12 weeks
  • Once daily 5nights per week 70
  • Twice daily 7 nights per week 76
  • Once daily 3 nights/ week 60
  • Cure Rates 6 weeks
  • Similar

32
MOHS MICROGRAPHIC SURGERY
  • Definition
  • The multistage excision of (non-melanoma skin)
    cancer using meticulous histologic examination of
    horizontal sections of removed tissue to guide
    the excision.
  • Allows maximal preservation of normal tissue with
    the highest published cure rates for selected
    tumors.

33
MOHS MICROGRAPHIC SURGERY
  • Useful for difficult tumors with lower cure rates
    with standard methods
  • Recurrent
  • Large
  • Difficult Anatomic Locations on Face
  • Clinically indistinct (ie margins difficult to
    ascertain)
  • Aggressive Pathology (Sclerosing)

34
WHERE TO CUT?
3 - 4mm margin
35
2. Excise Stage 1
1. Debulk
Mohs Micrographic Surgery
2. Excise Stage 1
Initial Defect
36
1. Debulk
3. Prepare Tissue
Initial Defect
37
Prepare Tissue (Patient Waits)
38
Taking residual Tumor - Stage II
Map Stage 1 Positive
39
Repairing Defect
Clear Margins
40
  • Hierarchy of Options
  • 2nd Intention
  • Primary Closure
  • Skin Graft
  • -FTSG
  • -STSG
  • Local Flap
  • -Advancement
  • -Rotation
  • -Transposition
  • -Pedicle
  • 2-Stage Local Flap
  • Combination Repair
  • Other
  • -Free Flap
  • -Tissue Expansion

41
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The End
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