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Skin Cancer and Melanoma
Chapter 24
Skin Cancer: How common is it?
 Skin cancer including melanoma,
basal and squamous cell skin cancers
[nonmelanoma]-most commonly
diagnosed of all types of cancers
 Other: Actinic or solar Keratosis
 Accounts for at least ½ of all cancers
 Melanoma cases have been
increasing over the yearsCopyright © 2014 by Mosby, an imprint of Elsevier Inc.
2
What is Skin Cancer?
 Skin-largest organ in
body
 3 layers & many cells
1. _________________
2. _________________
3. _________________
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
3
Skin Care
Health Promotion
 Avoidance of environmental hazards
 Adequate hygiene and nutrition
 Skin self-examination
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
4
Skin Care
Environmental Hazards
 Overexposure to sunlight
 Major cause of skin cancer
 Irritants and allergens
 Radiation
 Sleep
 Exercise
 Hygiene
 Nutrition Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
5
Pathophysiology
 Overexposure to
sunlight
 Ultraviolet radiation
(UV) to exposed area
 UV radiation changes
genetic (DNA)
material in cells
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
6
Wave Lengths of Sun & Effects on
Skin
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
7
Malignant Skin Neoplasms
 Self-examination
 ABCDE Rule
 Asymmetry
 Border irregularity
 Color change
 Diameter >6 mm
 Evolving in
appearance
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
8
Risk Factors
 Chronic UV light
exposure
 Fair skin, freckles,
light hair
 Family hx of skin CA
 Exposure to tar and
systemic arsenicals
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
9
Fitzpatrick Classification of Skin
Type
 Type I (very white or
freckled): Always
burn
 Type II (white):
Usually burn
 Type III (white to
olive): Sometimes
burn
 Type IV (brown):
Rarely burn
 Type V (dark brown):
Very rarely burn
 Type VI (black):
Never burn
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
10
Nonmelanoma Skin Cancers
 Basal cell or squamous cell-most common
 Actinic or solar keratosis
 Most common etiologic factor: ___________
 Develop in the __________________________
 Sites:
 __________________________
 _________________________________
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
11
Nonmelanoma Skin Cancers
 Actinic keratosis [____________]
 Premalignant skin lesions
 Common chronically sun damaged skin
 Population affected: _____________________
 Small [1-10 mm] macule or papule w/dry, rough
adherent yellow or brown scale
[_________________________]
 Clinical appearance:
 Irregularly shaped, flat or elevated, slightly erythematous
base with indistinct borders; hard keratotic scale or horn
 Distribution:
___________________________________________Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
12
Nonmelanoma Skin Cancers
 Actinic Keratosis
 Rx/Prognosis
 Cryosurgery [liquid nitrogen], chemical
peels, laser resurfacing
 Photodynamic therapy followed by
light irradiation
 Chemotherapy agents
 Fluorouracil [5-FU] topical & Imiquimod
[Aladara]Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
13
Nonmelanoma Skin CA
 Basal cell carcinoma [BCC]
 Arises from the basal cell layer of skin
 Population: __________________
 Metastasis is rare
 Risk factors: genetic skin type
disposition and chronic irritation [x-
ray, radiation, scars and some types of
nevi [moles];
 most common: _____________Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
14
Nonmelanoma Skin CA
 Clinical findings: BCC
 Nodular & ulcerative: small, slow
enlarging pearly papule w/central
crater and rolled waxy borders
 Borders semi-translucent or “pearly”
with overlying telangiectasia &
freckles visible on inspection
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
15
Nonmelanoma Skin CA
 Clinical findings: BCC
 Superficial: erythematous, pearly,
sharply defined, barely elevated
plaques
 Distribution:
 Sun-exposed areas
 ____________________________________
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
16
Nonmelanoma Skin CA
 Diagnostic: tissue bx-confirms
 Multiple Rx modalities
 Surgical excision, electrodessication,
curettage, cryosurgery, radiation
 Topical or systemic chemotherapy
 5-Fu and imiquimod: superficial lesions
 Vismodegib [Erivedgel]:
 Photodynamic therapy
 Small lesionsCopyright © 2014 by Mosby, an imprint of Elsevier Inc.
17
Basal Cell Carcinoma
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
18
Nonmelanoma Skin Cancers
 Squamous cell carcinoma [SCC]
 Malignant neoplasm of the epidermis
 Aggressive; potential to metastasize;
death if untreated
 Most frequent: __________________
 _____________: formation of lesions on
mouth and lips; ear and external
genitalia [more likely to invade &
spread] Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
19
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
20
Nonmelanoma Skin Cancers
 SCC
 Superficial: thin, scaly, red plaque
w/out invasion into dermis
 Early: firm nodules w/indistinct
borders, scaling and ulceration
 Late: lesion covered w/scale or horn
from keratinization ulceration;
indurated margins
 Distribution:___________________Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
21
Nonmelanoma Skin Cancers
 SCC
 Course: Rapid invasion w/mets via
lymphatics
 Tx
 Surgical excision, cryosurgery,
radiation, chemo, electrodessication,
curettage
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
22
Atypical/Dysplastic Nevus
 Dysplastic nevi (DN):
______________
 Greater than 5 mm
across; irregular borders
 Various shades
 Same ABCD
characteristics as
melanoma
 May be precursor of
malignant melanomaCopyright © 2014 by Mosby, an imprint of Elsevier Inc.
23
 Pigmented CA arising in melanin-producing epidermal
cells
 Irregularly shaped pigmented papule or plaque
w/varied colors: red, white and blue, black, gray or
brown; flat or elevated; eroded or ulcerated
 Highly metastatic; survival depends on early dx &
treatment
 Cause unknown
 Environmental factors
 Genetic factors
 1ST DEGREE relative: parent, sibling
Malignant Melanoma
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
24
Malignant Melanoma
 Distribution: anywhere on body/ or where
moles or birthmarks are evident
 Commonly found: ________________
_______________________________________
_________________________
 Course
 Horizontal growth pattern followed by vertical growth pattern
 Rapid invasion & mets w/high morbidity/mortality
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
25
 Risk factors
 Red or blonde hair
 Light-colored eyes; Fair skin that
freckles
 Chronic sun exposure
 Artificial sources of UV radiation
 Family history
 Use of immunosuppressive drugs and
hx of nevi: increase risk
Malignant Melanoma
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
26
 Diagnosis
 Suspicious, pigmented lesions: NOT
Shave-biopsied, shave-excised,
electrocauterized
 MelaFind
 Tumor thickness
 Breslow measurement:________________
 Clark level:___________________________
Malignant Melanoma
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
27
Breslow
Breslow measurement of tumor thickness. A,
Thin (0.08 mm) superficial spreading melanoma,
good prognosis. B, Thick nodular melanoma
with lymph node involvement, poor prognosis.
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
28
Copyright © 2014 by Mosby, an imprint of
Elsevier Inc.
 Collaborative care
 Treatment determined by
 Site of original tumor
 Stage of the cancer
 Patient’s age and general health
 Includes surgical incision and adjuvant therapy
[chemo, biologic therapy [i.e. interferon,
interleukin-2 or radiation]
 Chemo: dacarbazine [DTIC], temozolomide
[Temodar], procarbazine [Matulane], carmustine
[BCNU] and lomustine [CCNU]
 Newer t
Malignant Melanoma
29
Collaborative Care
 Assessment
 H&P
 Family hx of skin CA
 Hx past sx for removal of skin growths
 Recent changes in size, color or sensation of any mole, birthmark,
wart or scar
 Ask about geographical location of residence; occupational and
recreational activities
 Ask if severe skin injury has resulted in a scar
 Examine skin surface for any unusual lesions, moles, warts,
birthmarks and scars & Palpate lesions to determine surface
textue
 Document location, size/color/surface & subjective reports of
tenderness/itching
 Use ABCDE method to evaluateCopyright © 2014 by Mosby, an imprint of Elsevier Inc.
30
Collaborative Care
 Collaborative care
 Treatment determined by
 Site of original tumor
 Stage of the cancer
 Patient’s age and general health
 Includes surgical incision and adjuvant therapy [chemo, biologic
therapy [i.e. interferon, interleukin-2 or radiation]
 Chemo:
 dacarbazine [DTIC], temozolomide [Temodar], procarbazine [Matulane],
carmustine [BCNU] and lomustine [CCNU]
 Newer [metastatic]
 Ipilimumab [Yevoy]- monoclonal AB-locks onto CTL-4
 vemurafenib [Zelboral], dabrafenib [Tafinlar], trametinib
[Mekinist]:gene mutation BRAF V600
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
31
Collaborative Care
 Topical chemotherapy
 5-fluorouracil [5-Fu] cream
 Multiple actinic keratosis
 Widespread superficial BCC
 As lesions crust,ooze and erode: treated
areas more tender & inflamed
 Unsightly appearance
 Post D/C tx: coop com;resses
 Topical steroidCopyright © 2014 by Mosby, an imprint of Elsevier Inc.
32
 Tumor staging
 O–IV
 Tumor size
 Nodal involvement
 Metastasis
 T-N-M
Malignant Melanoma
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
33
Copyright © 2014 by Mosby, an imprint of
Elsevier Inc.
Diagnostic and Surgical Therapy
 Electrodesiccation
 Curettage
 Cryosurgery
 Excision—
 Mohs procedure or surgery
 Wide excision
34
Health Promotion & Maintenance
 Avoid or reduce exposure to sun
 Avoiding direct sunlight
 Using sunscreen
 Wear protective clothing [hats]
 TEACH ALL TO AVOID TANNING BEDS & SALONS
 Secondary prevention, early detection-critical-
 Teach to be aware of their skin markings
 Keep total body spot & lesion map
 Monthly total skin self-examination [TSSE]
 Teach ABCDE guide for melanoma
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
35
Copyright © 2014 by Mosby, an imprint of
Elsevier Inc.
Case Study
 E.N., a 45-year-old white female
with strawberry blonde hair and blue
eyes, works at a garden center.
 She has come to the dermatology
clinic because she noticed that the
mole on her left shoulder has
increased in size and darkened in
color.
Jupiterimages/Comstock/Thinkstock
36
Case Study
 You assess E.N.’s mole and note
that it is 5 mm x 8 mm in diameter,
shaped like a jagged pebble.
 She describes the changes she has
noticed: the color has changed from
brown to black and it has increased
in size and feels bumpy.
Jupiterimages/Comstock/Thinkstock
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
37
Case Study
 A shave biopsy is done on E.N.’s
mole.
 Diagnosis of malignant melanoma is
confirmed.
 What factors will determine the next
steps in treatment?
Jupiterimages/Comstock/Thinkstock
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
38
Case Study
 E.N. has her mole excised and her
axillary lymph nodes on the right
side are dissected to assess for
metastasis.
 Lymph nodes are negative for cancer
cells.
Jupiterimages/Comstock/Thinkstock
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
39
Case Study
 E.N. questions the type of surgery
that was performed and how it was
determined that all of the tumor was
excised.
 What type of surgical procedure was
likely used to excise the mole?
Jupiterimages/Comstock/Thinkstock
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
40
Case Study
 Postoperatively, E.N. examines her
shoulder.
 She tearfully expresses concern
regarding the size of the incision and
its location on her shoulder.
Jupiterimages/Comstock/Thinkstock
Copyright © 2014 by Mosby, an imprint of Elsevier Inc.
41

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Skin ca

  • 1. Skin Cancer and Melanoma Chapter 24
  • 2. Skin Cancer: How common is it?  Skin cancer including melanoma, basal and squamous cell skin cancers [nonmelanoma]-most commonly diagnosed of all types of cancers  Other: Actinic or solar Keratosis  Accounts for at least ½ of all cancers  Melanoma cases have been increasing over the yearsCopyright © 2014 by Mosby, an imprint of Elsevier Inc. 2
  • 3. What is Skin Cancer?  Skin-largest organ in body  3 layers & many cells 1. _________________ 2. _________________ 3. _________________ Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 3
  • 4. Skin Care Health Promotion  Avoidance of environmental hazards  Adequate hygiene and nutrition  Skin self-examination Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 4
  • 5. Skin Care Environmental Hazards  Overexposure to sunlight  Major cause of skin cancer  Irritants and allergens  Radiation  Sleep  Exercise  Hygiene  Nutrition Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 5
  • 6. Pathophysiology  Overexposure to sunlight  Ultraviolet radiation (UV) to exposed area  UV radiation changes genetic (DNA) material in cells Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 6
  • 7. Wave Lengths of Sun & Effects on Skin Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 7
  • 8. Malignant Skin Neoplasms  Self-examination  ABCDE Rule  Asymmetry  Border irregularity  Color change  Diameter >6 mm  Evolving in appearance Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 8
  • 9. Risk Factors  Chronic UV light exposure  Fair skin, freckles, light hair  Family hx of skin CA  Exposure to tar and systemic arsenicals Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 9
  • 10. Fitzpatrick Classification of Skin Type  Type I (very white or freckled): Always burn  Type II (white): Usually burn  Type III (white to olive): Sometimes burn  Type IV (brown): Rarely burn  Type V (dark brown): Very rarely burn  Type VI (black): Never burn Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 10
  • 11. Nonmelanoma Skin Cancers  Basal cell or squamous cell-most common  Actinic or solar keratosis  Most common etiologic factor: ___________  Develop in the __________________________  Sites:  __________________________  _________________________________ Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 11
  • 12. Nonmelanoma Skin Cancers  Actinic keratosis [____________]  Premalignant skin lesions  Common chronically sun damaged skin  Population affected: _____________________  Small [1-10 mm] macule or papule w/dry, rough adherent yellow or brown scale [_________________________]  Clinical appearance:  Irregularly shaped, flat or elevated, slightly erythematous base with indistinct borders; hard keratotic scale or horn  Distribution: ___________________________________________Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 12
  • 13. Nonmelanoma Skin Cancers  Actinic Keratosis  Rx/Prognosis  Cryosurgery [liquid nitrogen], chemical peels, laser resurfacing  Photodynamic therapy followed by light irradiation  Chemotherapy agents  Fluorouracil [5-FU] topical & Imiquimod [Aladara]Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 13
  • 14. Nonmelanoma Skin CA  Basal cell carcinoma [BCC]  Arises from the basal cell layer of skin  Population: __________________  Metastasis is rare  Risk factors: genetic skin type disposition and chronic irritation [x- ray, radiation, scars and some types of nevi [moles];  most common: _____________Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 14
  • 15. Nonmelanoma Skin CA  Clinical findings: BCC  Nodular & ulcerative: small, slow enlarging pearly papule w/central crater and rolled waxy borders  Borders semi-translucent or “pearly” with overlying telangiectasia & freckles visible on inspection Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 15
  • 16. Nonmelanoma Skin CA  Clinical findings: BCC  Superficial: erythematous, pearly, sharply defined, barely elevated plaques  Distribution:  Sun-exposed areas  ____________________________________ Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 16
  • 17. Nonmelanoma Skin CA  Diagnostic: tissue bx-confirms  Multiple Rx modalities  Surgical excision, electrodessication, curettage, cryosurgery, radiation  Topical or systemic chemotherapy  5-Fu and imiquimod: superficial lesions  Vismodegib [Erivedgel]:  Photodynamic therapy  Small lesionsCopyright © 2014 by Mosby, an imprint of Elsevier Inc. 17
  • 18. Basal Cell Carcinoma Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 18
  • 19. Nonmelanoma Skin Cancers  Squamous cell carcinoma [SCC]  Malignant neoplasm of the epidermis  Aggressive; potential to metastasize; death if untreated  Most frequent: __________________  _____________: formation of lesions on mouth and lips; ear and external genitalia [more likely to invade & spread] Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 19
  • 20. Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 20
  • 21. Nonmelanoma Skin Cancers  SCC  Superficial: thin, scaly, red plaque w/out invasion into dermis  Early: firm nodules w/indistinct borders, scaling and ulceration  Late: lesion covered w/scale or horn from keratinization ulceration; indurated margins  Distribution:___________________Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 21
  • 22. Nonmelanoma Skin Cancers  SCC  Course: Rapid invasion w/mets via lymphatics  Tx  Surgical excision, cryosurgery, radiation, chemo, electrodessication, curettage Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 22
  • 23. Atypical/Dysplastic Nevus  Dysplastic nevi (DN): ______________  Greater than 5 mm across; irregular borders  Various shades  Same ABCD characteristics as melanoma  May be precursor of malignant melanomaCopyright © 2014 by Mosby, an imprint of Elsevier Inc. 23
  • 24.  Pigmented CA arising in melanin-producing epidermal cells  Irregularly shaped pigmented papule or plaque w/varied colors: red, white and blue, black, gray or brown; flat or elevated; eroded or ulcerated  Highly metastatic; survival depends on early dx & treatment  Cause unknown  Environmental factors  Genetic factors  1ST DEGREE relative: parent, sibling Malignant Melanoma Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 24
  • 25. Malignant Melanoma  Distribution: anywhere on body/ or where moles or birthmarks are evident  Commonly found: ________________ _______________________________________ _________________________  Course  Horizontal growth pattern followed by vertical growth pattern  Rapid invasion & mets w/high morbidity/mortality Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 25
  • 26.  Risk factors  Red or blonde hair  Light-colored eyes; Fair skin that freckles  Chronic sun exposure  Artificial sources of UV radiation  Family history  Use of immunosuppressive drugs and hx of nevi: increase risk Malignant Melanoma Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 26
  • 27.  Diagnosis  Suspicious, pigmented lesions: NOT Shave-biopsied, shave-excised, electrocauterized  MelaFind  Tumor thickness  Breslow measurement:________________  Clark level:___________________________ Malignant Melanoma Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 27
  • 28. Breslow Breslow measurement of tumor thickness. A, Thin (0.08 mm) superficial spreading melanoma, good prognosis. B, Thick nodular melanoma with lymph node involvement, poor prognosis. Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 28
  • 29. Copyright © 2014 by Mosby, an imprint of Elsevier Inc.  Collaborative care  Treatment determined by  Site of original tumor  Stage of the cancer  Patient’s age and general health  Includes surgical incision and adjuvant therapy [chemo, biologic therapy [i.e. interferon, interleukin-2 or radiation]  Chemo: dacarbazine [DTIC], temozolomide [Temodar], procarbazine [Matulane], carmustine [BCNU] and lomustine [CCNU]  Newer t Malignant Melanoma 29
  • 30. Collaborative Care  Assessment  H&P  Family hx of skin CA  Hx past sx for removal of skin growths  Recent changes in size, color or sensation of any mole, birthmark, wart or scar  Ask about geographical location of residence; occupational and recreational activities  Ask if severe skin injury has resulted in a scar  Examine skin surface for any unusual lesions, moles, warts, birthmarks and scars & Palpate lesions to determine surface textue  Document location, size/color/surface & subjective reports of tenderness/itching  Use ABCDE method to evaluateCopyright © 2014 by Mosby, an imprint of Elsevier Inc. 30
  • 31. Collaborative Care  Collaborative care  Treatment determined by  Site of original tumor  Stage of the cancer  Patient’s age and general health  Includes surgical incision and adjuvant therapy [chemo, biologic therapy [i.e. interferon, interleukin-2 or radiation]  Chemo:  dacarbazine [DTIC], temozolomide [Temodar], procarbazine [Matulane], carmustine [BCNU] and lomustine [CCNU]  Newer [metastatic]  Ipilimumab [Yevoy]- monoclonal AB-locks onto CTL-4  vemurafenib [Zelboral], dabrafenib [Tafinlar], trametinib [Mekinist]:gene mutation BRAF V600 Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 31
  • 32. Collaborative Care  Topical chemotherapy  5-fluorouracil [5-Fu] cream  Multiple actinic keratosis  Widespread superficial BCC  As lesions crust,ooze and erode: treated areas more tender & inflamed  Unsightly appearance  Post D/C tx: coop com;resses  Topical steroidCopyright © 2014 by Mosby, an imprint of Elsevier Inc. 32
  • 33.  Tumor staging  O–IV  Tumor size  Nodal involvement  Metastasis  T-N-M Malignant Melanoma Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 33
  • 34. Copyright © 2014 by Mosby, an imprint of Elsevier Inc. Diagnostic and Surgical Therapy  Electrodesiccation  Curettage  Cryosurgery  Excision—  Mohs procedure or surgery  Wide excision 34
  • 35. Health Promotion & Maintenance  Avoid or reduce exposure to sun  Avoiding direct sunlight  Using sunscreen  Wear protective clothing [hats]  TEACH ALL TO AVOID TANNING BEDS & SALONS  Secondary prevention, early detection-critical-  Teach to be aware of their skin markings  Keep total body spot & lesion map  Monthly total skin self-examination [TSSE]  Teach ABCDE guide for melanoma Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 35
  • 36. Copyright © 2014 by Mosby, an imprint of Elsevier Inc. Case Study  E.N., a 45-year-old white female with strawberry blonde hair and blue eyes, works at a garden center.  She has come to the dermatology clinic because she noticed that the mole on her left shoulder has increased in size and darkened in color. Jupiterimages/Comstock/Thinkstock 36
  • 37. Case Study  You assess E.N.’s mole and note that it is 5 mm x 8 mm in diameter, shaped like a jagged pebble.  She describes the changes she has noticed: the color has changed from brown to black and it has increased in size and feels bumpy. Jupiterimages/Comstock/Thinkstock Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 37
  • 38. Case Study  A shave biopsy is done on E.N.’s mole.  Diagnosis of malignant melanoma is confirmed.  What factors will determine the next steps in treatment? Jupiterimages/Comstock/Thinkstock Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 38
  • 39. Case Study  E.N. has her mole excised and her axillary lymph nodes on the right side are dissected to assess for metastasis.  Lymph nodes are negative for cancer cells. Jupiterimages/Comstock/Thinkstock Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 39
  • 40. Case Study  E.N. questions the type of surgery that was performed and how it was determined that all of the tumor was excised.  What type of surgical procedure was likely used to excise the mole? Jupiterimages/Comstock/Thinkstock Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 40
  • 41. Case Study  Postoperatively, E.N. examines her shoulder.  She tearfully expresses concern regarding the size of the incision and its location on her shoulder. Jupiterimages/Comstock/Thinkstock Copyright © 2014 by Mosby, an imprint of Elsevier Inc. 41

Hinweis der Redaktion

  1. Skin cancer is the most commonly diagnosed cancer. Skin cancers are either nonmelanoma or melanoma. Highest among light-skinned people and older than 60 years of age Highest among those that work outdoors, live at higher altitudes or lower latitudes or spend significant amount of time sunbathing Occupational exposure to arsenic or other chemical carcinogens also increases risk Incidence of melanoma has increased during the past 30 years accounting for 2% of all cancers and 1% of all cancers deaths (ACS, 2011). A persistent skin lesion that does not heal is highly suspicious for malignancy and should be examined by a health care provider
  2. Skin cancers are name for the type of cell that become cancer. Three layers: Epidermis, Dermis and Subcutaneous tissue (fat or adipose tissue) Epidermis is the outermost skin layer. Attached to the basement membrane are the keratinocytes, the actual skin cells. The keratinocytes capable of cell division are the basal cells, which are located closest to the basement membrane and continuously divide to form new cells. Melanocytes are pigment-producing cells found at the basement membrane. Melanocytes are contained in the deep, basal layer (stratum germinativum) of the epidermis. These cells give color to the skin and account for the ethnic differences in skin tone. They contain melanin, a pigment that gives color to the skin and hair and protects the body from damaging ultraviolet (UV) sunlight. Sunlight and hormones stimulate the melanosome (within the melanocyte) to increase the production of melanin. Dermis (corium) is the layer above the fat layer. It is composed of connective tissue that contains no cells. The dermis is composed of collagen and elastic fibers that are interwoven to give the skin both flexibility and strength. Collagen forms the greatest part of the dermis and is responsible for the skin's mechanical strength. Subcutaneous fat (adipose tissue [fat]) is the innermost layer of the skin, lying over muscle and bone.
  3. Years of exposure to the sun are cumulative and damaging. The ultraviolet (UV) rays of the sun cause degenerative changes in the dermis, resulting in premature aging. Prolonged and repeated sun exposure is a major factor in precancerous and cancerous lesions. Actinic keratosis, basal cell carcinoma, squamous cell carcinoma, and malignant melanoma are dermatologic problems that are associated with direct or indirect sun exposure. Patients should recognize that sun safety guidelines include sun avoidance (especially during the midday hours), protective clothing, and sunscreen. Other factors that increase the possibility of sunburn include being at high altitude; being in snow, which reflects 80% of the sun’s rays; or being in or near water. Sunscreens can filter both UVA and UVB wavelengths. Patients can seek treatment for irritant or allergic dermatitis, which are two types of contact dermatitis. Irritant contact dermatitis is produced by direct chemical injury to the skin. Allergic contact dermatitis is an antigen-specific, type IV delayed hypersensitivity response. X-rays are valuable in both diagnosis and therapy but can cause serious side effects to the skin, including erythema, dry and moist desquamation, edema, and hypopigmentation and hyperpigmentation. Sleep is restorative to the skin, as well as to the rest of the body. Pruritic skin diseases often interfere with sleep. Adequate rest increases the patient’s ability to tolerate itching, thereby decreasing skin damage from the resultant scratching. Exercise increases circulation and dilates the blood vessels. In addition to the healthy glow produced by exercise, the psychologic effects can also improve one’s appearance and mental outlook. Hygienic practices are influenced by the skin type, lifestyle, and culture of the patient. The use of mild, moisturizing soaps (e.g., Ivory) and lipid-free cleansers, as well as avoiding hot water and vigorous scrubbing, can noticeably decrease local skin irritation and inflammation. A well-balanced diet adequate in all food groups can produce healthy skin, hair, and nails. Important elements include Vitamins A, B complex, C, D3, and K; protein and unsaturated fats.
  4. Specific wavelengths of the sun have different effects on the skin. Sunlight is composed of visible light and UV light. There are two types of UV light: UVA and UVB. UVA light is responsible for tanning and UVB for sunburn. Both types can damage the skin and increase the risk of skin cancer. Both UVA and UVB can cause collagen damage and accelerate the aging of skin. Tanning is the skin's response to injury and is caused by the increased production of melanin. When sun exposure is excessive, the turnover time of the skin becomes shortened, which can result in peeling. Fair-skinned persons should be especially cautious about excessive sun exposure because they have less melanin and thus less natural protection.
  5. Teach patients to self-examine their skin at least on a monthly basis. Cornerstone of skin self-examination: ABCDE Rule: The ABCDEs of melanoma. A, Asymmetry: one half unlike the other half. B, Border irregularity: edges are ragged, notched, or blurred. C, Color: varied pigmentation; shades of tan, brown, and black. D, Diameter: greater than 6 mm (diameter of a pencil eraser). E, (not pictured) Evolving; changing appearance (change in shape, size, color, or other characteristic is noted over time).
  6. Risk factors for skin malignancies include having a fair skin type (blond or red hair and blue or green eyes), history of chronic sun exposure, family history of skin cancer, and exposure to tar and systemic arsenicals. Environmental factors that increase the risk of skin malignancies include living near the equator, outdoor occupations, and frequent outdoor recreational activities. Risk factors are anything that can increase or decrease a person’s chance of getting the disease such as CA. There are many known risk factors for the more common forms of skin CA. Some cannot be changed [nonmodifiable] and others can be changed [modifiable]. Behavioral factors such as using indoor tanning booths and outdoor sunbathing are controllable risk factors for skin malignancies Risk for skin cancer is higher for light skin people versus darker skin people
  7. Fitzpatrick classification of skin type can assist you in determining how a patient will respond or react to facial treatments, and how likely they are to get skin cancer. This system classifies skin into six different skin types, skin color, and reaction to sun exposure.
  8. NM skin CA are either basal cell or squamous cell-Most common forms of skin cancer Nonmelanoma skin cancers develop in the epidermis. Most common etiologic factor is SUN EXPOSURE The most common sites for the development of nonmelanoma skin cancer are in sun-exposed areas and include the face, head, neck, back of the hands, and arms. They do not develop from melanocytes, the skin cells that make melanin as melanoma skin cancers do. They do have the potential for severe local destruction, permanent disfigurement and disability Avoid exposure to midday sun and the use of protective clothing and sunscreen beginning early in life to help prevent formation of skin malignancies later in life.
  9. Actinic keratosis, also known as solar keratosis, consists of hyperkeratotic papules and plaques occurring on sun-exposed areas. Actinic keratoses are premalignant skin lesions that affect nearly all of the older white population. Most common of all premalignant skin lesions The clinical appearance of actinic keratoses can be highly varied. The typical lesion is an irregularly shaped, flat, slightly erythematous papule with indistinct borders and an overlying hard keratotic scale or horn (Table 24-3). They can be verrucous [wartlike]. Adherent scale returns when removed. Often many in number. Increase in # with age. Thick, indurated keratosis more likely to be malignant Distribution: cheeks, temples, forehead, ears, neck, backs of hands and forearms May progress to Squamous cell CA if lesions are untreated.
  10. May disappear spontaneously or reappear after adequate Rx Slow progression to SCC
  11. Basal cell carcinoma (BCC) is a locally invasive malignancy arising from epidermal basal cells. Population: Middle-aged to older adults Most common risk factor: UV light exposure It is the most common type of skin cancer and also the least deadly. Clinical manifestations are described in Table 24-3. The cancerous cells of BCC almost never spread beyond the skin but if not treated can cause massive tissue destruction.
  12. Pearly papule with a central crater and rolled waxy borders Telangiectasis and pigment freckles visible on close inspection Normal skin markings are lost
  13. Sun-exposed areas: especially head, neck and central portion of face
  14. Surgical excision, electrodessication, curettage, cryosurgery, radiation-90% cure rate Metastasis is rare Vismodegib is for metastatic or recurrent locally invasive lesions.
  15. Squamous cell carcinoma (SCC) is a malignant neoplasm of keratinizing epidermal cells. It frequently occurs on sun-exposed skin at the base of an actinic keratosis or another lesion. Chronic skin damage from repeated injury or irritation also predisposes to this malignancy. SCC is less common than BCC. SCC can be highly aggressive, has the potential to metastasize, and may lead to death if not treated early and correctly. Pipe, cigar, and cigarette smoking contribute to the formation of SCC on the mouth and lips. Lesions on ear, lip and external genitalia are more likely to invade and spread than those found elsewhere on the body.
  16. Late: fixated to underlying tissue w/deep invasion Distribution: sun exposed areas especially head, neck, and lower lip; sites of chronic irritation or injury [scars, irradiated skin, burns, leg ulcers
  17. Occurs in 10% of cases Larger tumors are more prone to metastasis Untreated lesion may spread to regional lymph nodes and distant organs High cure rate w/early detection and treatment
  18. An abnormal nevus pattern called dysplastic nevus syndrome identifies an individual at increased risk of melanoma. Approximately 2% to 8% of the white population has moles classified as atypical or dysplastic nevi. Dysplastic nevi (DN), or atypical moles, are nevi that are larger than usual (greater than 5 mm across) with irregular borders and various shades of color: tan, bown, black, red or pink within single mole. Presence of at least one single flat portion often at edge of mole. Most common site: back or in uncommon sites such as scalp or buttocks These nevi may have the same ABCDE characteristics as melanoma, but they are less pronounced. May be precursor of malignant melanoma-Increased risk for Melanoma Requires careful monitoring of persons suspected of familial tendency to melanoma or dysplastic nevi Suspeicious lesions: excisional biopsy
  19. Malignant melanoma is a tumor arising in melanocytes, which are the cells producing melanin. Melanoma causes the majority of skin cancer deaths. Mets to any organ including brain and heart. Death rate ten times higher in whites then in AA Accounts for 2% of all CA and 1% of all cancer deaths Combination of environmental and genetic factors are involved. Environment: higher incidence among those who work outdoors, live at higher altitudes or lower altitudes or spend significant amount of time sunbathing Occupational exposure: arsenic or other chemical carcinogens Genetic: A person may be born with a genetic disposition toward getting melanoma. Between 5% and 10% of people who develop melanoma have a first-degree relative (e.g., parent, sibling) who developed melanoma. Risk increases if multiple relatives have a history of melanoma. Genetic mutation inherited in an autosomal dominant pattern has been found for some cases of familial melanoma. Occurs in a suppressor gene resulting in loss of control of cell growth. Two such genes are CDKN2A, CDK4 and BRAF
  20. Commonly found: Back [males] chest, neck ; lower legs then back [females] Soles of feed and palms in dark skinned individuals On skin, it is called cutaneous melanoma but can also occur in eye, meninges, lymph nodes, GI tract and anywhere else in body where melanocytes are found Course: Horizontal growth pattern followed by vertical growth pattern; rapid invasion and mets w/high morbidity and mortality
  21. Incidence highest among light-skinned races; older than 60 and those with red or blonde hair. Although UV radiation from the sun is the main cause of melanomas and other skin cancer, artificial sources of UV radiation, such as sunlamps and tanning booths, also play a role. UV radiation damages the DNA in skin cells, creating “misspellings” in their genetic code causing cells to be altered. Although anyone can develop melanoma, the risk is greatest for people who have red or blond hair, blue or light-colored eyes or BLUE, and light-colored skin that freckles easily.
  22. Pigmented lesions suspicious for melanoma should not be shave-biopsied, shave-excised, or electrocauterized. Handheld screening devices (e.g., MelaFind) can assist the health care provider to determine whether a lesion without the obvious ABCDE signs should be biopsied. The most important prognostic factor is tumor thickness at the time of diagnosis. Two methods to determine thickness are currently being used. The Breslow measurement indicates the depth of the tumor in millimeters (Figure 24-5), and the Clark level indicates the depth of invasion of the tumor; the higher the number, the deeper the melanoma.
  23. Treatment depends on the site of the original tumor, the stage of the cancer, and the patient’s age and general health. The staging of melanoma (stages 0 to IV) is based on tumor size (thickness), nodal involvement, and metastasis. In stage 0 the melanoma is confined to one place (in situ) in the epidermis. Melanoma is nearly 100% curable by excision if diagnosed at stage 0. The 5-year survival rate depends on sentinel node biopsy results, which indicate if metastasis has occurred. If metastasis to other organs is found (stage IV), treatment then becomes palliative Initial treatment of malignant melanoma is surgical excision, which may require a skin graft to close. Melanoma that has spread to the lymph nodes or nearby sites usually requires additional (adjuvant) therapy such as chemotherapy, biologic therapy (e.g., α-interferon, interleukin-2), and/or radiation therapy.
  24. A careful history is of prime importance in the diagnosis of skin problems. After a careful history and physical examination, inspect individual lesions. Based on the history, physical examination, and appropriate diagnostic tests, either medical, surgical, or combination therapy is planned. Skin that has been injured previously is at greater risk for cancer development, an effect known as Koebner's phenomenon. Ask the patient if he or she has ever experienced a severe skin injury that resulted in a scar. Examine all scarred skin areas for the presence of potentially cancerous lesions. Also examine hair-bearing areas of the body, such as the scalp and genitalia. Palpate lesions to determine surface texture. Document the location, size, color, and surface features of all lesions and any subjective reports of tenderness or itching. Use the ABCDE method of evaluating all lesions for possible melanoma.
  25. Biotherapy with interferon is now an accepted treatment after surgery for melanomas that are at stage III or higher. The patient is first started on high-dose (20,000,000 units/m2) IV interferon infusions daily for 5 days per week for 4 weeks after the surgical wound is well healed. Maintenance doses of 10,000,000 units/m2 are continued three times per week for 1 year. The maintenance doses are given subcutaneously, and the patient must learn to self-inject the drug. Agents that target lymphocyte control of tumor cell growth may be used for treatment of metastatic melanoma. The approved drug ipilimumab (Yervoy) and the experimental drug tremelimumab target the CTLA4 (cytotoxic T-lymphocyte–associated antigen 4) receptor and block it, resulting in greater activity of the lymphocyte. This allows the lymphocyte to attack melanoma cells. Because the receptor is present on certain lymphocytes, the side effects of these drugs include significant inflammation in many tissues. Ipilimumab, a type of immunotherapy, is a monoclonal antibody that locks onto CTLA-4, a protein that normally helps keep T cells in check. By blocking the action of CTLA-4, ipilimumab boosts the immune response against melanoma cells. Vemurafenib, dabrafenib, and trametinib are used for patients whose melanoma tumors express a gene mutation called BRAF V600.
  26. Prepare pt for an unsightly appearance during therapy and reassure him or her that the cosmetic effect will be positive After tx is d/c, cool compresses and topical steroids to help decrease inflammation and promote comfort.
  27. The staging of melanoma (stages 0 to IV) is based on tumor size (thickness), nodal involvement, and presence of metastasis. In stage 0, the melanoma is confined to one place (in situ) in the epidermis. Melanoma is nearly 100% curable by excision if diagnosed at stage 0. Melanoma is nearly 100% curable by excision if diagnosed at stage 0. The 5-year survival rate depends on sentinel node biopsy results, which indicate if metastasis has occurred. If metastasis to other organs is found (stage IV), treatment then becomes palliative.
  28. Surgical and nonsurgical interventions are combined for the effective management of skin cancer. Treatment is determined by the size and severity of the malignancy, the location of the lesion, and the age and general health of the patient. Surgical Management Surgical intervention is the most common means of managing any type of skin cancer. It can range from local removal of small lesions, with minimal discomfort and positive cosmetic results, to massive excision of large areas of the skin and underlying tissue for treatment of melanoma Curettage and electrodesiccation may be used for small lesions that are not melanoma. This method can destroy the cancerous cells while minimizing damage to the surrounding uninvolved tissue. After a local anesthetic is given, the surgeon uses a dermal curette to scrape away the cancerous tissue. After curettage is complete, the surgeon places an electric probe on the wound and remnants of the tumor are destroyed by thermal energy. Wounds created by this treatment heal by second intention, and scarring is usually minimal. Instruct patients in caring for the wound, including cleaning the wound, using prescribed antibacterial drugs, and applying dressings. Cryosurgery is the use of subfreezing temperatures to destroy epidermal lesions. Cryosurgery is a useful treatment for common benign, precancerous conditions including common and genital warts, cutaneous tags, thin seborrheic keratoses, lentigines, actinic keratoses, and nonmelanoma skin cancers. Topical liquid nitrogen (−196°-200 F) is the agent most commonly used for cryosurgery. Excision is used for biopsy of small lesions. When the diagnosis is melanoma, a sentinel node may be biopsied to determine whether tumor spread has started. If the size and location of the lesion permit, surgical excision with primary closure is the preferred method. If the tumor has already been removed several times or if radiation therapy has damaged the surrounding skin, healing by second intention is indicated. This procedure allows the wound to be monitored for cancer recurrence. Skin grafts and flaps are used to repair large defects if tissue destruction is deep A specific type of excision is Mohs surgery, which is a microscopically controlled removal of a cutaneous malignancy. Mohs’ surgery, a specialized form of excision, is used to treat basal and squamous cell carcinomas. The cancerous tissue is sectioned horizontally in layers, and each layer is examined histologically to determine the presence of residual tumor cells. Although the procedure is long and tedious, cure rates are high and there is less removal of healthy tissue compared with other surgical methods. Wide excision for deeper melanoma or other skin cancers that are large or invasive often involves removing full-thickness skin in the area of the lesion. Depending on tumor depth, subcutaneous tissues and lymph nodes may also be removed.
  29. The single most effective prevention strategy for skin cancer is avoiding or reducing skin exposure to sunlight. However, even when people understand the cause of skin cancer and the seriousness of the disease, preventive behaviors are not always practiced. Secondary prevention, early detection, is critical to survival with melanoma. Teach all people to be aware of their skin markings. Keeping a total body spot and lesion map can provide baseline information about suspicious lesions and help identify changes in a lesion or lesions earlier. Once a map is made, the person should systematically inspect his or her body monthly for new lesions and for changes in any existing lesions by performing thorough skin self-examination (TSSE). Often a partner is needed to help evaluate skin spots or lesions on the back. Some people find taking pictures of their skin on a regular basis makes identifying changes easier. Teach everyone to evaluate all skin lesions using the ABCDE guide for melanoma and to consult his or her health care provider to examine any lesion having unusual characteristics. When lesions, such as moles, are present, they should be monitored yearly by a dermatologist or other health care professional. Monthly TSSE is critically important for patients who have already had a melanoma lesion. A major positive influence for TSSE practice is working with a partner in this examination.
  30. We are now going to walk through a case study and follow a patient through the diagnosis and treatment of a skin problem. What are the risk factors for this patient: Strawberry blonde hair Blue eyes Sun exposure Possible chemical exposure at work
  31. What other questions would you ask E.N. regarding her mole? How would she describe the original size, shape, and color of the mole? When did she notice the mole beginning to change? Does she have any pain at the site to palpation? Does she have any other moles of concern? How would you document assessment of the mole utilizing the ABCDE Rule? Asymmetrical: 5 mm x 8 mm Border irregularity: shaped like a jagged pebble Color changes: brown to black Diameter > 6 mm to 8 mm Evolving in appearance: Patient describes increasing size plus color change and texture change
  32. What are the possible treatment options for E.N.? (See next slide.)
  33. How would you expect this mole to be classified in terms of staging of E.N.’s tumor: stage 0 Would you expect E.N. to require additional treatment after excision? This is not required for a stage 0 tumor in which the entire margin of the mole is excised and the lymph nodes are negative. E.N. asks if this means her cancer is gone. How would you respond? The surgeon discusses the final outcome of the surgery and biopsy results. After this information is conveyed, you will be able to reinforce that the cancer has been removed and she will need to be watchful and report any new changes in this or other areas.
  34. The surgical procedures that was likely used to excise E.N.’s mole: Mohs procedure would be used to excise the tumor in layers, examining each layer to determine whether the margin and the depth of the tumor have been reached.
  35. Have students role play therapeutic exploration of E.N.’s feelings and best responses to her concerns. What are some suggestions that you could make to assist E.N. in adapting and camouflaging her scar? Wearing short sleeve shirts rather than sleeveless to conceal the scar Adding scarves, shawls to a sleeveless dress or blouse Try using makeup to conceal the scar when wearing sleeveless shirts, bathing suits, etc.