Malignant Melanoma
Definition
Malignant melanoma is a type of skin tumor that is characterized by the cancerous growth of melanocytes, which are cells that produce a dark pigment called melanin.
Description
Overview
Cancer of the skin is the most common type of cancer and continues to grow in incidence. Skin cancer starts in the top layer of skin (the epidermis) but can grow down into the lower layers, the dermis and the subcutaneous layer. There are three main types of cells located in the epidermis, each of which can become cancerous. Melanocytes are the pigmented cells that are scattered throughout the skin, providing protection from ultraviolet (UV) light. Basal cells rest near the bottom of the epidermis and the layer of cells that continually grow to replace skin. The third type of epidermal cell is the squamous cells which make up most of the cells in human skin.
Melanoma
Malignant melanoma is the most serious type of skin cancer. It develops from melanocytes. Although melanoma is the least common skin cancer, it is the most aggressive. It spreads (metastasizes) to other parts of the body—especially the lungs and liver—as well as invading surrounding tissues. Melanomas in their early stages resemble moles. In Caucasians, melanomas appear most often on the trunk, head, and neck in men and on the arms and legs in women. Melanomas in African Americans, however, occur primarily on the palms of the hand, soles of the feet, and under the nails. Melanomas appear only rarely in the eyes, mouth, vagina, or digestive tract. Although melanomas are associated with exposure to the sun, the greatest risk factor for developing melanoma may be genetic. People who have a first-degree relative (parent, sibling or child) with melanoma have an increased risk up to eight times greater of developing the disease.
Basal cell cancer
Basal cell cancer is the most common type of skin cancer, accounting for about 75% of all skin cancers. It occurs primarily on the parts of the skin exposed to the sun and is most common in people living in equatorial regions or areas of high ozone depletion. Light-skinned people are more at risk of developing basal cell cancer than dark-skinned people. This form of skin cancer is primarily a disease of adults; it appears most often after age 30, peaking around age 70. Basal cell cancer grows very slowly. If it is not treated, however, it can invade deeper skin layers and cause disfigurement. This type of cancer can appear as a shiny, translucent nodule on the skin or as a red, wrinkled and scaly area.
Squamous cell cancer
Squamous cell cancer is the second most frequent type of skin cancer. It arises from the outer keratinizing layer of skin, so named because it contains a tough protein called keratin. Squamous cell cancer grows faster than basal cell cancer; it is more likely to metastasize to the lymph nodes as well as to distant sites. Squamous cell cancer most often appears on the arms, head, and neck. Fair-skinned people of Celtic descent are at high risk for developing squamous cell cancer. This type of cancer is rarely life-threatening but can cause serious problems if it spreads and can also cause disfigurement. Squamous cell cancer usually appears as a scaly, slightly elevated area of damaged skin.
Other skin cancers
Besides the three major types of skin cancer, there are a few other relatively rare forms. The most serious of these is Kaposi's sarcoma (KS), which occurs primarily in persons who have AIDS or older males of Mediterranean descent. When KS occurs with AIDS it is usually more aggressive. Other types of skin tumors are usually nonmalignant and grow slowly. These include:
- Bowen's disease. This is a type of skin inflammation (dermatitis) that sometimes looks like squamous cell cancer.
- Actinic or solar keratosis. This is a sunlight-damaged area of skin that sometimes develops into cancer.
- Keratoacanthoma. A keratoacanthoma is a domeshaped tumor that can grow quickly and appear like squamous cell cancer. Although it is usually benign, it should be removed.
Risk factors
SUN EXPOSURE. Most skin cancers are associated with the amount of time that a person spends in the sun and the number of sunburns received, especially if they occurred at an early age. Skin cancer typically does not appear for 10-20 years after the sun damage has occurred. Because of this time lag, skin cancer rarely occurs before puberty and occurs more frequently with age.
MOLES. The number of moles (nevi) on a person's skin is related to the likelihood of developing melanoma. There are three types of nevi: not cancerous (benign); atypical (dysplastic); or birthmark (congenital). All three types of nevi have been associated with a higher risk of developing melanoma. Sometimes the moles themselves can become cancerous. Usually, however, the cancer is a new growth that occurs on normal skin.
HEREDITY.The tendency to develop skin cancer also tends to run in families. As has already been mentioned, there appears to be a significant genetic factor in the development of melanoma.
Causes and symptoms
Skin cancer begins to develop when a change or mutation occurs in one of the cells of the skin, causing it to grow without control. This mutation can be caused by ultraviolet (UV) light; most skin cancers are thought to be caused by overexposure to UV light from the sun. The incidence of severe, blistering sunburns is particularly closely related to skin cancer, more so when these burns occur during childhood. Exposure to ionizing radiation, arsenic, or polycyclic hydrocarbons in the workplace also
appears to stimulate the development of skin cancers. The use of psoralen for treatment of psoriasis may be associated with the development of squamous cell cancer. Skin cancers are also more common in immunocompromised persons, such individuals with AIDS or those who have undergone organ transplants.
The first sign of skin cancer is usually a change in an existing mole, the presence of a new mole, or a change in a specific area of skin. Any change in a mole or skin lesion, including changes in color, size, or shape, tenderness, scaliness, or itching should be suspected of being skin cancer. Areas that bleed or are ulcerated may be signs of more advanced skin cancer. By doing a monthly self-examination, a person can identify abnormal moles or areas of skin and seek evaluation from a qualified health professional. The ABCD rule provides an easy way to remember the important characteristics of moles when one is examining the skin:
- Asymmetry. A normal mole is round, whereas a suspicious mole is unevenly shaped.
- Border. A normal mole has a clear-cut border with the surrounding skin, whereas the edges of a suspect mole are often irregular.
- Color. Normal moles are uniformly tan or brown, but cancerous moles may appear as mixtures of red, white, blue, brown, purple, or black.
- Diameter. Normal moles are usually less than 0.20 in (5 mm) in diameter. A skin lesion greater than 0.25 in (0.6 cm) across may be suspected as cancerous.
There are two systems used in staging melanomas. The first is Clark's, which bases staging on the level of invasion, or which tissues the tumor has penetrated (i.e. which skin layer). The other is the American Joint Committee on Cancer. The second system is sometimes called the TNM system, which stands for tumor-nodesmetastasis, after the three major phases in cancer progression. Most experts generally agree that the thickness of the tumor is more accurate than the level of invasion for predicting prognosis (the outcome of the disease and estimated chance of recovery) and choosing an appropriate treatment.
Diagnosis
A person who has a suspicious-looking mole or area of skin should consult a doctor. In many cases, the person's primary care physician will make a referral to a doctor who specializes in skin diseases (a dermatologist). The dermatologist will carefully examine the lesion for the characteristic features of skin cancer. If further testing seems necessary, the dermatologist will perform a skin biopsy by removing the lesion under local anesthesia. Because melanomas tend to grow in diameter, as well as downwards into the epidermis and fatty layers of skin, a biopsy sample that is larger than the mole will be taken. This tissue is then analyzed under a microscope by a specialist in diseased organs and tissues (a pathologist). The pathologist makes the diagnosis of cancer and determines how far the tumor has grown into the skin. The evaluation of the progression of the cancer is called staging. Staging refers to how advanced the cancer is and is determined by the thickness and size of the tumor. Additional tests will also be done to determine if the cancer has moved into the lymph nodes or other areas of the body. These tests might include chest x ray, computed tomography scan (CT scan), magnetic resonance imaging (MRI), and blood tests.
Treatment
Surgery
The primary treatment for skin cancer is to cut out (excise) the tumor or diseased area of skin. Surgery usually involves a simple excision using a scalpel to remove the lesion and a small amount of normal surrounding tissue. A procedure known as microscopically controlled excision can be used to examine each layer of skin as it is removed to ensure that the proper amount is taken. Depending on the amount of skin removed, the cut is either closed with stitches or covered with a skin graft. When surgical excision is performed on visible areas, such as the face, cosmetic surgery may also be performed to minimize the scar. Other techniques for removing skin tumors include burning, freezing with dry ice (cryosurgery), or laser surgery. For skin cancer that is localized and has not spread to other areas of the body, excision may be the only treatment needed.
Nonsurgical approaches
Although chemotherapy is the normal course of therapy for most other types of advanced cancer, it is not usually effective and not usually used for advanced skin cancer. For advanced melanoma that has moved beyond the original tumor site, the local lymph nodes may be surgically removed. Immunotherapy in the form of interferon or interleukin is being used more often with success for advanced melanoma. There is growing evidence that radiation therapy may be useful for advanced melanoma. Other treatments under investigation for melanoma include gene therapy and vaccination. Recent studies have shown that the use of a vaccine prepared from a person's own cancer cells may be useful in treating advanced melanoma. For people previously diagnosed with skin cancers, the chances of getting additional skin cancers are high. Therefore, regular monthly self-examination, as well as frequent examinations by a dermatologist, are essential.
Alternative treatment
There are no established alternative treatments for skin cancer. Immunotherapy, which strengthens the immune system, is an approach that may prove valuable in the future. Preventive measures that can be helpful include minimizing exposure to the sun and sunburn, eating a diet high in antioxidants and supplementation with antioxidant nutrients.
Prognosis
The prognosis for skin cancer depends on several factors, the most important of which are the invasiveness of the tumor and its location. The prognosis is good for localized skin cancers that are diagnosed and treated early. For basal cell cancer and squamous cell cancer, the cure rate is close to 100%, although most people with these forms will have recurrent skin cancer. For localized melanoma, the cure rate is approximately 95%. The prognosis worsens with larger tumors. Melanoma that has spread to the lymph nodes has a 5-year survival rate of 54%; advanced melanoma has a survival rate of only 13%. When melanoma has spread to other parts of the body, it is generally considered incurable. The median length of survival is six months.
Health care team roles
A physician makes an initial diagnosis. A dermatologist and pathologist may confirm the diagnosis. A surgeon removes most lesions. A plastic and reconstructive surgeon may repair or minimize surgical scars. Nurses and nurse practitioners will participate in prevention education with patients.
Prevention
Prevention is the best way to approach skin cancer. Avoiding unnecessary sun exposure, from such sources as sun lamps and tanning salons, is relatively simple. Parents of small children should protect them against the risk of sunburn. Precautions include avoiding high sun, when the rays of the sun are most intense (between 11 A.M. and 1 P.M.). In addition, persons living at high elevations need to take extra precautions because the intensity of UV radiation increases by 4% with every 1,000-ft (305-m) rise above sea level. When outdoors protective clothing should be worn, covering exposed skin. Sunglasses with UV protective coating should also be worn.
There is presently some debate about the ability of sunscreen to protect against skin cancer. Some scientists believe that gradual exposure to the sun, in order to develop a mild tan, may offer the best protection from skin cancer. Skin cancer has also been related to diets that are high in fat. Decreasing the amount of fat consumed may also help to decrease the risk of skin cancer.
KEY TERMS
Biopsy—Removal of a small piece of tissue for examination. This is done under local anesthesia and removed by either using a scalpel or a punch, which removes a small cylindrical portion of tissue.
Cryosurgery—The use of extreme cold to destroy tissue in treating skin cancer.
Dermatologist—A doctor who specializes in skin diseases.
Epidermis—The outermost layer of skin.
Interferon—A group of proteins that have an effect on immune function and appear to have an anti-tumor effect in some persons.
Melanin—A dark pigment that is found in certain skin cells and helps to protect the skin from ultraviolet light.
Melanocyte—A specialized skin cell that produces melanin.
Metastasis—The movement of cancer cells from one area of the body to another through the blood or the lymph vessels.
Pathologist—A specialist in diseased organs and tissues.
Staging—The process of classifying and evaluating the progression of a cancer.
TNM staging—A staging system for classifying cancers developed by the American Joint Committee on Cancer. The initials stand for tumor, nodes, and metastasis.
Resources
BOOKS
Balch, Charles M. Cutaneous Melanoma, 3rd ed. St. Louis, Quality Medical Publishing, 1998.
Buchan, John and Roberts, Daffyd Lloyd. Pocket Guide to Malignant Melanoma. New York, Blackwell Science, 2000.
Darmstadt, Gary L. "Tumors of the skin." In Nelson Textbook of Pediatrics, 16th ed., edited by Richard E. Behrman et al. Philadelphia: W.B. Saunders, 2000, 2051-2053.
Parker, Frank. "Skin diseases of general importance." In Cecil Textbook of Medicine, 21st ed., edited by Goldman, Lee and Bennett, J. Claude. Philadelphia: W.B. Saunders, 2000, 2276-2298.
Poole, Catherine M. and Guerry, DuPont. New Haven, CT, Yale University Press, 1998.
Schofield, Jill R. and Robinson, William A. What You Really Need to Know About Moles and Melanoma. Baltimore: Johns Hopkins University Press, 2000.
Smithson, William A. "Cancer of the skin." In Nelson Textbook of Pediatrics, 16th ed., edited by Richard E. Behrman et al. Philadelphia: Saunders, 2000, 1566-1567.
Sober, Arthur J., Koh, Howard K., Tran, N-LT and Washington, Carl V. "Melanoma and other skin cancers." In Harrison's Principles of Internal Medicine, 14th ed., edited by Anthony S. Fauci, et al. New York: McGraw-Hill, 1998, 543-549.
PERIODICALS
Bedikian A.Y., Plager C., Stewart J.R., O'Brian C.A., Herdman S.K., Ross M., Papadopoulos N., Eton O., Ellerhorst J., Smith T. "Phase II evaluation of bryostatin1 in metastatic melanoma." Melanoma Research 11, no. 2(2001): 183-188.
Hillner B.E., Kirkwood J.M., Agarwala S.S. "Burden of illness associated with metastatic melanoma." Cancer 91, no. 9 (2001): 1814-1821.
Lucci A., Citro H.W., Wilson L. "Assessment of knowledge of melanoma risk factors, prevention, and detection principles in Texas teenagers." Journal of Surgical Research 97, no. 2 (2001): 179-183.
Naylor M.F. "Melanoma vaccines." Dermatology Online Journal 6, no. 1 (2000): 5-9.
Shore R.E. "Radiation-induced skin cancer in humans." Medical and Pediatric Oncology 36, no. 5 (2001): 549-554.
Taran J.M., Heenan P.J. "Clinical and histologic features of level 2 cutaneous malignant melanoma associated with metastasis." Cancer 91, no. 9 (2001): 1822-1825.
ORGANIZATIONS
American Academy of Dermatology, 930 N. Meacham Road, PO Box 4014, Schaumburg, IL 60168-4014. (847) 330-0230. Fax: (847) 330-0050. <http://www.aad.org>.
American Melanoma Foundation, 3914 Murphy Canyon Road, Suite A132, San Diego, CA 92123. (858) 277-4426. <http://www.melanomafoundation.org/homepage.html>. sunsmartz@melanomafoundation.org.
Melanoma Education Foundation, 7 Jones Road, Peabody, MA 01960. <http://www.skincheck.com/#Site%20Content>. MEF@skincheck.org.
Melanoma Research Foundation, 23704-5 El Toro Rd., #206, Lake Forest, CA 92630. Phone/Fax: (800) 673-1290. mrf@melanoma.org.
National Cancer Institute, Building 31, Room 10A31, 31 Center Drive, MSC 2580, Bethesda, MD 20892-2580.(800) 422-6237 or (301) 435-3848. http://www.nci.nih.gov/.
Skin Cancer Foundation, 245 5th Avenue Suite 1403, New York, NY 10016. (800) 754-6490. Fax: (212) 725-5751. <http://www.skincancer.org/melanoma/>, info@skincancer.org.
OTHER
American Academy of Dermatology. <http://www.aad.org/SkinCancerNews/WhatIsSkinCancer/ABCDMel.... >.
Melanoma Foundation of Australia. <http://www.med.usyd.edu.au/medicine/melanoma/>.
National Library of Medicine. <http://www.nlm.nih.gov/medlineplus/melanoma.html>.
National Melanoma Foundation. <http://www.nationalmelanoma.org/>.
University of California-Davis. <http://matrix.ucdavis.edu/tumors/new/tutorial-intro.html>.
University of Maryland. <http://umm.drkoop.com/conditions/ency/article/001442.htm>.
University of Pennsylvania. <http://cancer.med.upenn.edu/disease/melanoma/>.
L. Fleming Fallon, Jr., M.D., Dr.P.H.
