Skin cancer is very common, with melanoma and non-melanoma skin cancers accounting for over half of all cancers. The main risk factor for skin cancer is overexposure to ultraviolet radiation from sunlight, which can damage skin cells' DNA. Early detection of skin cancers through monthly skin self-exams and recognition of warning signs like moles that change size or color is important for treatment and prevention of metastasis. Treatment options depend on the type and stage of skin cancer and may involve surgical excision, chemotherapy, radiation, or newer targeted therapies.
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
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.
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.
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.
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).
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
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.
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.
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.
May disappear spontaneously or reappear after adequate Rx
Slow progression to SCC
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.
Pearly papule with a central crater and rolled waxy borders
Telangiectasis and pigment freckles visible on close inspection
Normal skin markings are lost
Sun-exposed areas: especially head, neck and central portion of face
Surgical excision, electrodessication, curettage, cryosurgery, radiation-90% cure rate
Metastasis is rare
Vismodegib is for metastatic or recurrent locally invasive lesions.
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.
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
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
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
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
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
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.
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.
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.
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.
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.
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.
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.
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.
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.
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
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
What are the possible treatment options for E.N.? (See next slide.)
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.
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.
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.