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Recognizing Neoplastic Skin Lesions: A Photo Guide
- LEWIS C. ROSE, M.B., B.S.(LOND),
- University of Texas Health Science Center, San Antonio, Texas
A patient information handout on skin cancer, written by the author of this article, is provided on page 887.
Malignant lesions of the skin are common. Patients who develop squamous cell carcinoma and malignant melanoma often have recognizable precursor conditions. A few skin lesions resemble malignancies. Lesions that are growing, spreading or pigmented, or those that occur on exposed areas of skin are of particular concern. Knowing the similarities and differences between these lesions allows the primary physician to make a diagnosis in most cases by simple inspection and palpation. When in doubt, it is appropriate to perform an excisional biopsy of small lesions or punch biopsy of larger lesions. Removal of premalignant lesions will reduce the occurrence of malignant disease. Almost all skin cancers can be cured by early excision or destruction. For these reasons, physicians should be aware of the risk factors for skin cancer, educate patients about risk reduction and include skin inspection for premalignant and malignant lesions as a part of routine health maintenance examinations.
Primary neoplastic disease of the skin is common. Early recognition of such lesions is important because complete excision will cure almost all cases of skin cancer if performed in the early stages. A presumptive diagnosis can often be made by considering the patient's risk factors, the history of the lesion and its location, appearance and texture. The definitive diagnosis is made by histologic examination of biopsy specimens.
A complete skin examination performed at regular intervals is important in adults, since the early stages of skin cancer are often asymptomatic and inconspicuous. Factors that Contribute to Skin Cancer
Most primary skin neoplasms occur in skin that is exposed to adverse conditions. Ultraviolet light from sunlight is most often a contributing factor. Desert sunlight is particularly dangerous, but water and snow both reflect a high proportion of the ultraviolet light from the sky, increasing the risk for sailors, beach lovers and winter-sports enthusiasts. In farmers and ranchers, the skin of the face, neck and arms is also at high risk.
Exposure to immunosuppressive drugs or ionizing radiation is a less common cause.1 Use of organic arsenics and tars predisposes to skin cancer. A history of malignant melanoma in a first-degree relative or the presence of numerous melanotic nevi, which may be familial or sporadic, greatly increases the risk of developing malignant melanoma.2-4 Persons with fair or freckled skin that does not tan are at increased risk. Dark hair and skin provide some protection from skin cancer. Family physicians should educate their patients about these risks and encourage them to protect their skin.
Basal cell carcinomas account for most skin cancers. These lesions are usually located on the face and other exposed areas of the skin. Skin lesions come to the attention of the physician in three ways: (1) the patient may be aware of the lesion and consult the physician about it; (2) the physician may notice the lesion when examining the patient for some other reason; or (3) the physician inspects the entire skin surface for lesions as part of a pre-employment or health maintenance examination. A complete skin examination is important particularly in high-risk patients because, at the stage when they are curable, skin cancers are painless and often inconspicuous. The top of the head, the face, the neck, the shoulders and the extensor surfaces of the arms are particularly important, but the areola, the vulva and the foreskin are also areas of high risk. In black patients, the palms of the hands, soles of the feet and periungual areas are particularly vulnerable. A detailed description and measurement of all suspicious skin lesions should be documented in the patient's medical record.
Basal Cell Carcinoma
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Figure 1. Small basal cell carcinoma.![]()
Figure 2. Basal cell carcinoma with the characteristic shiny appearance.![]()
Figure 3. Ulcerating basal cell carcinoma.Comprising 60 percent of primary skin cancers, the basal cell carcinoma is a slow-growing lesion that invades tissue but rarely metastasizes. Most metastatic basal cell carcinomas arise from large tumors.5 Basal cell carcinomas that have recurred after excision may be at greater risk of metastasis.6 Basal cell carcinoma is common on the face and on other exposed skin surfaces but may occur anywhere (Figure 1). The common form first appears as a small round or oval area of skin thickening. Usually there is no itching, pain or change in skin color. The area very slowly extends circumferentially, creating a slightly raised edge, which may have a shiny, pearly or slightly translucent appearance (Figure 2).
As the lesion continues to grow, the central area becomes atrophic, leaving a hollow that is covered by thin skin, often with visible vessels, which eventually ulcerates (Figure 3). The growing edges become more irregular, and the shape becomes uneven. The base is also invasive and gradually erodes the underlying tissue, making it difficult to excise the lesion completely.
Less common forms include a superficial basal cell carcinoma that resembles a patch of dermatitis, a pigmented basal cell carcinoma that resembles a nodular malignant melanoma and an aggressive-growth basal cell carcinoma. Aggressive-growth basal cell carcinoma is an infiltrating sclerosing lesion that may appear similar to a scar with a firm or hard base. In patients younger than 35 years, basal cell carcinoma tends to adopt the more aggressive forms.7
No premalignant conditions precede basal cell carcinoma. Basal cell carcinoma and lesions of similar appearance are compared in Table 1.
Squamous Cell Carcinoma
Squamous cell carcinoma comprises 20 percent of all cases of skin cancer. It typically occurs on areas of the skin that have been exposed to sunlight for many years. It may also appear in areas that have been subjected to ionizing irradiation or in other locations in patients who have undergone treatment with immunosuppressive drugs1 or have been exposed to organic trivalent arsenic compounds or tars. Squamous cell carcinoma of the lip may be related to pipe smoking, as well as to sunlight exposure.
Human papillomavirus infection may be a precursor of keratoacanthoma and periungual, genital and other squamous cell carcinomas, especially in immunosuppressed patients.8 The affected area develops a slight redness, scaling, fissuring and an uneven surface. Superficial dilated vessels may be visible. The lesion often appears very dry and may bleed when stretched or abraded. It spreads laterally from the edges and may heap up irregularly. New lesions often appear near old ones. Clusters of lesions may occur as fleshy masses (Figure 4). The centers may become atrophic and develop raw patches or frank ulceration (Figure 5).
TABLE 1
Features of Basal Cell Carcinoma and Lesions of Similar AppearanceLesion
Location
Surface
Color
Outline
Other features
Basal cell carcinoma Most common on face, but can occur anywhere Raised, pearly, firm Normal skin color Round at first, irregular later May ulcerate Superficial basal cell carcinoma Any location Roughened Skin-colored or pink Round or irregular Resembles dermatitis Pigmented basal cell carcinoma Most commonly occurs on the face Nodule Growing area is dark brown or black Becomes irregular as growth progresses Looks like a nodular malignant melanoma Infiltrating basal cell carcinoma Any location Smooth Skin-colored Various Looks like a firm scar that grows aggressively Tricoepithelioma Any location Raised, pearly Normal skin color Round Does not become malignant Keloid Site of previous injury Raised, rounded, smooth Usually pink, may be skin-colored Varies, often linear Often large, but no growth after one year Molluscum contagiosum Face and hands of children, areas of sexual contact Raised, rounded central hollow
Soft, fleshySkin-colored Round Usually multiple, in clusters or scattered; contagious Dermatofibroma Often occurs on limbs, rarely on face Flat or slightly raised, edge not thickened or pearly Skin-colored, firm under the surface but not on the surface Usually round or oval Usually >5 mm diameter when first noticed Two other skin lesions are considered part of the squamous cell carcinoma spectrum. The first type, keratoacanthoma, is closely related to squamous cell carcinoma. Like squamous cell carcinoma, it appears on skin damaged by sunlight or chemicals. It often occurs at the site of trauma, especially in immunosuppressed patients. It is sometimes associated with human papillomavirus infection. Keratoacanthoma appears as a skin-colored or pink smooth lesion, which becomes dome-shaped during a period of very rapid growth. When mature, it is volcano-shaped, with protruding masses of keratin resembling lava. Classic keratoacanthoma is not malignant and regresses spontaneously, but atypical lesions may actually be squamous cell carcinoma.7 Many dermatopathologists include keratoacanthoma in the spectrum of squamous cell carcinoma9 (Figure 6).
The second type is verrucous carcinoma, a variant of squamous cell carcinoma that features an irregular warty surface (Figure 7).
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Figure 4. Squamous cell carcinoma showing clusters of lesions.
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Figure 6. Keratoacanthoma with typical volcano appearance.
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Figure 5. Ulcerating squamous cell carcinoma of the lip.
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Figure 7. Irregular warty surface of verrucous carcinoma.While metastasis of common sunlight-induced squamous cell carcinoma is unusual, lesions more likely to metastasize are lesions of the lip or ear, lesions that recur after previous therapy, lesions at the site of a burn and those that are more deeply invasive. Squamous cell carcinoma of the skin may be metastatic from other locations (Figure 8).
A variety of skin lesions are considered precursors of squamous cell carcinoma. Actinic keratosis appears very similar to the less severe lesions of squamous cell carcinoma. It is always found on skin that has received heavy exposure to sunlight.9,10 Actinic keratosis should be sought during routine inspection of the skin, especially in fair-skinned patients who have been exposed to sunlight frequently. Regular reexamination of affected skin and treatment of any areas showing growth or change can prevent neoplastic transformation or provide early treatment of malignancy11 (Figure 9).
Epidermodysplasia verruciformis is an uncommon autosomal recessive disorder that predisposes patients to the development of squamous cell carcinoma (Figure 10). Actinic cheilitis is a condition that is similar to actinic keratitis but occurs on the vermilion of the lips.
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Figure 8. Metastatic squamous cell carcinoma.
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Figure 9. Actinic keratosis.
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Figure 10. Epidermodysplasia verruciformis of the hand.
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Figure 11. Erythroplasia of Queyrat (Bowen's disease of the penis).
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Figure 12. Leukoplakia of the genital area.Bowen's disease is squamous cell carcinoma in situ that resembles a plaque of psoriasis. When Bowen's disease occurs on the penis, it is called erythroplasia of Queyrat (Figure 11). Leukoplakia of the mouth or genital area may be premalignant (Figure 12).
Human papillomavirus includes several strains that are associated with squamous cell carcinoma, especially in the genital areas.12 The virus may not be a precursor of squamous cell carcinoma but does increase the patient's risk for developing squamous cell carcinoma. In Table 2, squamous cell carcinoma and its variants are compared with other lesions of similar appearance (Figures 13 through 16).
TABLE 2
Features of Squamous Cell Carcinoma and Lesions of Similar AppearanceLesion
Location
Surface
Color
Outline
Other features
Squamous cell carcinoma Areas exposed to sunlight, radiation or arsenicals Rough, irregular, sometimes scaly, sometimes has visible vessels, sometimes warty or with fleshy masses Skin-colored at first, sometimes reddened later Vague New lesions may appear near old ones
Does not clear with cortico-steroid therapyKeratoacanthoma (a variant of squamous cell carcinoma) Exposed areas, especially face and hands Smooth dome, becoming volcano-shaped Skin-colored or slightly reddened Well-defined Goes through a period of very rapid growth, often regresses Eczema and atopic dermatitis (Figure 13) Atopic dermatitis behind ears, on flexure areas Reddened, slightly scaly, sometimes with vesicles Dry at first, fissured, may weep Indefinite Common in atopic persons and those exposed to irritants Contact dermatitis (Figure 14) Wherever skin comes in contact with an irritant Reddened, slightly scaly, sometimes with vesicles Dry at first, fissured, may weep Circumscribed Dermatitis clears with corticosteroid therapy Psoriasis (Figure 15) Elbows, knees, scalp, sacral cleft, nails Scaly with underlying reddened base White dry scales, smooth pink or red where scales are removed; may bleed Well-demarcated; round, irregular or confluent Often widespread, sometimes itchy; varies with season Seborrheic dermatitis (Figure 16) Scalp, forehead, nasolabial fold, midline trunk Raised, with scales Yellow or brown Well-demarcated Some lesions can be easily removed Malignant Melanoma
Although it comprises only 1 percent of skin cancers, malignant melanoma accounts for over 60 percent of skin cancer deaths.13 It metastasizes to remote sites early, and its metastases are characteristically unresponsive to treatment. Like the other skin cancers, malignant melanoma is more common on skin that has undergone excessive exposure to sunlight, but it can occur anywhere. Four types of malignant melanoma are identified.
The lesions of superficial spreading melanoma are dark brown or black. In the initial phase they have a slowly spreading irregular outline. Some areas may be a lighter shade. Vertical growth occurs later, penetrating into the dermis and causing some parts of the lesion to become raised. This is the most common kind of melanoma (Figure 17).
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Figure 13. Eczema dermatitis.
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Figure 14. Contact dermatitis.
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Figure 15. Psoriasis.
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Figure 16. Seborrheic dermatitis.
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Figure 17. Superficially spreading malignant melanoma.
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Figure 18. Lentigo maligna. Note the multiple nodules signaling invasiveness of the lesion.Nodular melanoma grows vertically from the start and is more likely to mestastasize early. It has little or no lateral extension, appearing as a shiny black dome.
Lentigo maligna melanoma occurs in a pre-existing lentigo maligna. The appearance of one or more nodules signals the change to an invasive lesion (Figure 18).
Acral lentiginous melanoma occurs on the palms of the hands, the soles of the feet, under the nails and on mucosal surfaces. It is uncommon, comprising only 5 percent of melanomas in pale-skinned persons. Dark-skinned persons rarely get melanomas, but if they do, the lesions are likely to be acral melanomas (Figure 19).
Since not all malignant melanomas are visibly pigmented, physicians should be suspicious of any lesion that is growing or that bleeds on minor trauma. If the diagnosis is in doubt, it is better to take one or more adequate full skin thickness biopsies for histologic examination.
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Figure 19. Acral lentiginous melanoma.
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Figure 20. Blue nevi.
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Figure 21. Common melanocytic nevi.
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Figure 22. Malignant melanoma.
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Figure 23. Pigmented basal cell carcinoma.
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Figure 24. Kaposi's sarcoma.Certain skin lesions are considered precursors of malignant melanoma. Blue nevi occasionally become the site of melanocytic malignant change. Suspicious features, such as location on the scalp of men in their forties, growth, bleeding on minor trauma and the occurrence of dark satellite lesions around the nevus, may signal this change. All blue nevi should be carefully monitored or excised (Figure 20).
Lentigo maligna (melanotic freckle of Hutchison) occurs on the face or other sun-exposed skin of older, fair-skinned persons. It is a brown macule with some color variation, spreading slowly and unevenly at the edges. Dark invasive lesions with irregular borders may grow from it (Figure 18). Congenital nevomelanocytic nevi are brown patches of skin that are present at birth or develop in infancy. They usually have an irregular surface, and they may be slightly raised and exhibit coarse hair. Lesions that are more than 20 cm across are more likely to undergo neoplastic change into malignant melanoma, often when the child is between three and five years of age.
The presence of 10 or more dysplastic nevi confers a 12-fold risk of developing malignant melanoma.2 Dysplastic nevi may appear de novo or may develop from common melanocytic nevi.3 They occur in 5 percent of the general white population, but in 30 to 50 percent of those with sporadic (nonfamilial) primary melanoma and in almost all patients with familial cutaneous melanoma.4
In Table 3, the common varieties of malignant melanoma are compared with lesions of similar appearance (Figures 21 through 23).
TABLE 3
Features of Four Forms of Malignant Melanoma and Lesions of Similar AppearanceLesion
Location
Surface
Color
Outline
Other features
Superficially spreading malignant melanoma Most common on sun-exposed skin, but can occur anywhere Smooth; vertical growth occurs later Dark brown or black, may be variegated Becomes more irregular as it grows May have a pink or reddish halo Nodular melanoma Most common on sun-exposed skin, but can occur anywhere Nodular form Dark brown or black, may be variegated May be regular or irregular Grows aggressively, invades early Lentigo maligna melanoma In a pre-existing lentigo maligna, usually facial Nodular against a smooth background Dark or black on pale brown background Irregular Acral lentiginous melanoma Nailbeds, palms of the hands, soles of the feet, mucosal areas Smooth Dark brown or black Irregular Occurs in both black and white persons Common melanocytic nevi (Figure 21) Widely scattered Smooth, flat or uniformly elevated Uniform light or dark brown Regular, round or oval, rarely >10 mm diameter Less common in black persons Lentigo (freckles) Mainly on sun-exposed surfaces Smooth, flat brown or tan Uniform light Round, oval or polyhedric Darken with sun exposure, lighten in winter Blue nevi (Figure 20) Most commonly occur on hands or feet; may occur anywhere Papules or nodules Blue, blue-gray, or blue-black Round or oval, usually <10 mm diameter Firm on palpation Pigmented basal cell carcinoma (Figure 23) Most common on the face Nodule Growing area is dark brown or black Becomes irregular as growth progresses Other Primary Malignancies of the Skin
Pigmented skin lesions can be evaluated using the "ABCD" rule: assymetry, border irregularity, color variation and diameter of 6 mm or greater. Kaposi's sarcoma appears as intensely red, nonblanching, slightly raised or nodular lesions of the skin and mucous membranes. Usually there are many lesions of various sizes. It occurs more frequently in patients with acquired immunodeficiency syndrome (Figure 24).
Sebaceous carcinoma has a nonspecific appearance similar to that of a squamous cell carcinoma of the skin, with nodularity, telangiectasias and hair loss (Figure 25).
Malignant eccrine spiradenoma is a slowly growing, deeply invasive sclerotic plaque that occurs on the face of older women. It is often painful (Figure 26).
Syringoid sweat duct carcinoma is a rare malignant condition that occurs on the face or scalp of elderly patients, causing local hair loss. The surface may be warty and secrete fluid (Figure 27).
Paget's disease of the nipple appears to be an unresponsive eczema of the areola but actually is a carcinoma in the ducts of the breast that grows outward to involve the skin.
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Figure 25. Sebaceous carcinoma at the outer angle of the left eye.
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Figure 26. Malignant eccrine spiradenoma.
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Figure 27. Syringoid sweat duct carcinoma. Note the characteristic warty appearance.
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Figure 28. Dysplastic nevi cascade.Pigmented lesions that appear suspicious can be evaluated by using the "ABCD" rules: asymmetry, border irregularity, color variation and diameter 6 mm or greater.14,15 Two other suspicious signs are more rapid growth than other lesions and the presence of a narrow pink halo around the lesion.
Squamous cell carcinoma may be treated by excision, cryotherapy or topical chemotherapy; it should be diagnosed by full skin thickness punch biopsies. For basal cell carcinoma and other skin malignancies, it is better to remove the lesion completely whenever possible, with lateral and deep margins of several millimeters of healthy tissue. If any of the ABCD signs are found in a new pigmented lesion or in a melanocytic nevus that was previously uniformly colored, smooth, flat, round or oval (Figure 28), an excisional biopsy should be performed. All suspicious lesions should be excised down to a connective tissue base with a 2- to 3-mm lateral margin.15
If a cosmetically acceptable result would be difficult to obtain after excisional biopsy, full skin thickness punch biopsy of several areas may be performed, including the margins and any raised areas. If a biopsy shows dysplasia, the whole lesion should be removed with 5-mm margins using plastic surgical techniques, and the site should be monitored for recurrence. Malignant melanoma also requires excision with a margin of at least 5 mm, and many dermatologists recommend a 2-cm margin. All other pigmented lesions that occur in these patients should be observed for change at least annually. Serial photographs may be valuable.16
Final Comment
Physicians should assist patients in reducing factors that increase the risk for developing skin cancer. A complete skin examination for premalignant and malignant lesions should be performed during periodic health evaluations and when other opportunities occur. By doing so, the vigilant physician can intervene and reduce the morbidity and mortality of malignant skin disease. Excisional biopsy with an adequate margin is recommended whenever possible. For a large lesion, multiple punch biopsies of selected areas, including the growing edge, is an acceptable method for reaching a diagnosis. In these cases the definitive excision will require plastic surgical techniques. Mohs' micrographic surgery is a technique in which the histology of each layer of tissue is determined before removing the next layer. This technique permits complete excision without excessively large margins.17,18
Figures 1, 3, 5, 7, 8, 10-12, 15-22, and 24-27 from the Division of Dermatology, Department of Medicine, University of Texas Health Science Center, San Antonio, Tex. Figures 2, 4, 6, 9, 13, 14, 23 and 28 from the American Academy of Family Physicians.
Each year members of a different family practice department develop articles for "Problem-Oriented Diagnosis." This series is coordinated by the Department of Family Practice at the University of Texas Health Science Center at San Antonio. Guest editors of the series are David A. Katerndahl, M.D., and Clinton Colmenares.
The Author
LEWIS C. ROSE, M.B., B.S.(LOND),
is an associate professor in the Department of Family Practice at the University of Texas Health Science Center at San Antonio. He received his medical training at University College Hospital Medical School, London, England. Dr. Rose is board certified in family practice in the United Kingdom, Canada and the United States.Address correspondence to Lewis C. Rose, M.B., B.S.(Lond), Department of Family Practice, University of Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78284. Reprints are not available from the author.
REFERENCES
- Shamanin V, zur Hausen H, Lavergne D, Proby CM, Leigh IM, Neumann C, et al. Human papillomavirus infections in nonmelanoma skin cancers from renal transplant recipients and nonimmunosuppressed patients. J Natl Cancer Inst 1996;88:802-11.
- Tucker MA, Halpern A, Holly EA, Hartge P, Elder DE, Sagebiel RW, et al. Clinically recognized dysplastic nevi. A central risk factor for cutaneous melanoma. JAMA 1997;227:1439-44.
- Swerdlow AJ, English J, Mackie RM, O'Doherty CJ, Hunter JA, Clark J, et al. Benign melanocytic naevi as a risk factor for malignant melanoma. Br Med J 1986;292:1555-9.
- Elder DE, Goldman LI, Goldman SC, Greene MH, Clark WH Jr. Dysplastic nevus syndrome: a phenotypic association of sporadic cutaneoous melanoma. Cancer 1980;46:1787-94.
- Snow SN, Sahl W, Lo JS, Mohs FE, Warner T, Dekkinga JA, et al. Metastatic basal cell carcinoma. Report of five cases. Cancer 1994;73:328-35.
- Tavin E, Persky MS, Jacobs J. Metastatic basal cell carcinoma of the head and neck. Laryngoscope 1995;105(8 Pt 1):814-7.
- Netscher DT, Wigoda P, Green LK, Spira M. Keratoacanthoma: when to observe and when to operate and the importance of accurate diagnosis. South Med J 1994;87:1272-6.
- de Villiers EM, Lavergne D, McLaren K, Benton EC. Prevailing papillomavirus types in non-melanoma carcinomas of the skin in renal allograft recipients. Int J Cancer 1997;73:356-61.
- Krunic AL, Garrod DR, Smith NP, Orchard GS, Cvijetic OB. Differential expression of desmosomal glycoproteins in keratoacanthoma and squamous cell carcinoma of the skin: an immunohistochemical aid to diagnosis. Acta Derm Venereol 1996;76: 394-8.
- Marks R. The role of treatment of actinic keratoses in the prevention of morbidity and mortality due to squamous cell carcinoma. Arch Dermatol 1991; 127:1031-3.
- Dodson J, DeSpain J, Hewett JE, Clark DP. Malignant potential of actinic keratoses and controversy over treatment. Arch Dermatol 1991;127:1029-31.
- Leffell D, Headington JT, Wong DS, Swanson NA. Aggressive-growth basal cell carcinoma in young adults. Arch Dermatol 1991;127:1663-7.
- Sauer GC, Hall JC, eds. Skin tumors. In: A manual of skin diseases. 7th ed. Philadelphia: Lippincot-Raven, 1996:342.
- Friedman RJ, Rigel DS, Kopf AW. Early detection of malignant melanoma: the role of the physician examination and self-examination of the skin. CA Cancer J Clin 1985;35:130-51.
- Roberson JK. A 28-year-old fair-skinned woman with multiple moles. JAMA 1997;278:1693-9.
- Shriner DL, Wagner RF Jr, Glowczwski JR. Photography for the early diagnosis of malignant melanoma in patients with atypical moles. Cutis 1992;50:358-62.
- Nelson BR, Railan D, Cohen S. Mohs' micrographic surgery for nonmelanoma skin cancers. Clin Plast Surg 1997;24:705-18.
- Zitelli JA, Brown CD, Hanusa BH. Surgical margins for excision of primary cutaneous melanoma. J Am Acad Dermatol 1997;37(3 Pt 1):422-9.
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Primary neoplastic disease of
the skin is common. Early recognition of such lesions is important because
complete excision will cure almost all cases of skin cancer if performed in the
early stages. A presumptive diagnosis can often be made by considering the
patient's risk factors, the history of the lesion and its location, appearance
and texture. The definitive diagnosis is made by histologic examination of
biopsy specimens.