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Melanoma is a very deadly form of Skin Cancer.
Please read the following Melanoma information provided by the MayoClinic. It just may save your life or the life of a loved one.
Melanoma is the most serious and deadly type of skin cancer. Melanoma develops in the cells that produce melanin — the pigment that gives your skin its color. Melanoma can also form in the eyes and, rarely, in internal organs, such as the intestines.
Although melanomas make up the smallest percentage of all skin cancers, they cause the greatest number of deaths. That's because they're more likely to spread to different parts of the body. And the incidence of melanoma is on the rise.
The exact cause of all melanomas isn't clear, but exposure to ultraviolet (UV) radiation from sunlight or tanning lamps and beds greatly increases the risk of developing melanoma.
Avoiding excessive sun exposure can prevent many melanomas. And knowing the warning signs of skin cancer can help ensure that cancerous changes are detected and treated before they have a chance to spread. Melanoma can be successfully treated if you catch it early.
Moles — the medical term is "nevi" — are clusters of pigmented cells. Normal moles are generally a uniform color, such as tan, brown or black, with a distinct border separating the mole from your surrounding skin. They're oval or round in shape and about 1/4 inch (6 millimeters) in diameter — the size of a pencil eraser.
Most people have between 10 and 40 moles. Many of these develop by age 20. Moles may change in appearance over time — and some may even disappear with age. Some people may have one or more large (more than 1/2 inch, or 12 millimeters, in diameter), flat moles with irregular borders and a mixture of colors, including tan, brown, and either red or pink. Known medically as dysplastic nevi, these moles are much more likely to become cancerous (malignant) than normal moles are.
What to look for
The first sign of melanoma is often a change in an existing mole or the development of a new, unusual-looking growth on the skin. To detect melanomas or other skin cancers, use the A-B-C-D skin self-examination guide, adapted from the American Academy of Dermatology:
What else to watch for
Other suspicious changes in a mole may include:
Malignant moles vary greatly in appearance. Some may show all of the changes listed above, while others may have only one or two unusual characteristics. Melanomas can develop anywhere on your body, but most often develop in areas that have had exposure to the sun, such as your back, legs, arms and face.
Hidden melanomas
Melanomas can also develop in areas of your body that have little or no exposure to the sun, such as the spaces between your toes and on your palms, soles, scalp or genitals. These are sometimes referred to as hidden melanomas because they occur in places most people wouldn't think to check. Hidden melanomas include:
Common types of melanomas
Most melanomas occur in more conspicuous places. The most common melanomas include:
Sometimes people mistake seborrheic keratoses for skin cancer. Seborrheic keratoses are waxy yellow, brown or black growths that look as if they've been pasted on your skin. What causes them is unknown, but they tend to be numerous and occur commonly in people over age 40. The growths are never cancerous, but they can closely mimic a skin cancer. You may want them removed if they become irritated by clothing or for cosmetic reasons.
Although it's common to think of skin in cosmetic terms — how soft, smooth or resilient it is — your skin is your body's largest organ and performs a number of essential functions, including regulating your body temperature and protecting your body's other organs from ultraviolet radiation, injury and infection.
Your skin consists of three layers — the epidermis, dermis and subcutis. The epidermis, the topmost layer, is as thin as a pencil line. It provides a protective layer of skin cells that your body continually sheds. Squamous cells lie just below the outer surface. Basal cells, which produce new skin cells, are at the bottom of the epidermis. The epidermis also contains cells called melanocytes, which produce melanin — the pigment that gives skin its normal color. When you're in the sun, these cells produce more melanin, which helps protect the deeper layers of skin. The extra melanin is what produces the darker color of a tan. The ability to produce melanin and the way it's distributed in the skin is genetically determined; people who sunburn easily simply form less pigment than do those who tan well.
Normally, skin cells within the epidermis develop in a controlled and orderly way. In general, healthy new cells push older cells toward the skin's surface, where they die and eventually are sloughed off. This process is controlled by DNA — the genetic material that contains the instructions for every chemical process in your body. But when DNA is damaged, changes occur in these instructions. One result is that new cells may begin to grow out of control and eventually form a mass of malignant cells. How well the body repairs DNA damage is genetically determined, but it also can be affected by certain medical conditions.
Just what damages DNA in skin cells and how this leads to melanoma is a matter of intense study. Cancer is a complex disease that often results from a combination of factors rather than from a single cause. Still, excessive exposure to ultraviolet (UV) radiation is a leading factor in the development of melanoma, whether the radiation is from the sun or from tanning lamps and beds.
UV radiation and skin cancer
UV radiation is a wavelength of sunlight in a range too short for the human eye to see. Commercial tanning lamps and tanning beds also produce UV radiation. UV light is divided into three wavelength bands — ultraviolet A (UVA), ultraviolet B (UVB) and ultraviolet C (UVC). Only UVA and UVB rays reach the earth — UVC radiation is completely absorbed by atmospheric ozone, a naturally occurring substance that filters UV radiation.
At one time scientists believed that only UVB rays played a role in the development of melanoma. And UVB light does cause harmful changes in skin cell DNA, including the development of oncogenes — a type of gene that can turn a normal cell into a malignant one. But UVA light may damage melanocytes. Tanning lamps and beds mainly produce UVA radiation.
UV radiation is most intense at the equator and at high elevations, but no matter where you live, your skin absorbs UV radiation whenever you're outdoors unless you wear protective clothing and sunscreen.What's more, exposure to occasional periods of intense sunlight puts you at risk of melanoma even more than does spending long hours in the sun. An initial high dose of UV radiation will severely damage melanocytes, but not destroy them. When these damaged cells are subjected to further intense bouts of UVA light, they have little capacity to repair their DNA and so are more likely to become malignant.
Other factors in melanoma
Chronic sun exposure doesn't explain all melanomas, and recent studies suggest that sun-induced melanomas may not be as aggressive as melanomas from other causes. Other factors that may lead to melanoma include:
As with other types of cancer, it's likely that many melanomas result from a combination of environmental and genetic factors.
Factors that may increase your risk of skin cancer include:
Fair skin. Having less pigment (melanin) in your skin means you have less protection from damaging UV radiation. If you have blond or red hair, light-colored eyes and you freckle or sunburn easily, you're more likely to develop melanoma than is someone with a darker complexion. Fair-skinned people of Northern European ancestry are particularly at risk. Queensland, Australia, has the highest skin cancer rate in the world because it has unusually high levels of UV radiation and because most of its inhabitants are of English or Irish descent.
Though less common, melanoma can develop in people with darker complexions, including Hispanics and blacks. For these people, melanoma is often diagnosed in the later stages, when the lesions are deeper and more advanced. Survival from melanoma is related almost entirely to the depth of invasion at the time of diagnosis. So it's important that people of all ethnic backgrounds be aware of melanoma and take precautions against UV radiation.
The American Cancer Society (ACS) recommends skin exams every three years for adults between ages 20 and 40 and yearly exams after age 40. These screening exams involve a head-to-toe inspection of your skin by someone qualified to diagnose skin cancer, such as a dermatologist or nurse specialist. If you have risk factors for skin cancer — fair skin, a history of severe sunburns, one or more dysplastic moles, or a family history of melanoma — talk to your doctor about more frequent screenings. Sometimes frequent screenings are recommended for all close family members of a person with melanoma.
In addition, the ACS recommends monthly self-exams for everyone older than 18. This helps you learn the moles, freckles and other skin marks that are normal for you, so you can notice any unusual changes. It's best to do this standing in front of a full-length mirror while using a hand-held mirror to inspect hard-to-see areas. Be sure to check the fronts, backs and sides of your arms and legs; your groin, scalp and fingernails; and your soles and the spaces between your toes.
If you notice a new skin growth, a change in an existing mole or a sore that doesn't heal in two weeks, see your doctor. Sometimes cancer can be detected simply by looking at your skin, but the only way to accurately diagnose melanoma is with a biopsy. In this procedure, your doctor or dermatologist removes all or part of the suspicious mole or growth, and a pathologist analyzes the sample.
If the mole is small, your doctor is likely to perform an excisional biopsy — such as a punch biopsy or an elliptical excision. In this procedure, the entire mole or growth is removed, along with a small border of normal-appearing skin. An incisional biopsy is more likely to be used for large moles, or for those on your hands or face, where scars are more obvious. In that case, only the most irregular part of a mole or growth is taken for laboratory analysis. Contrary to common belief, incisional biopsies don't cause melanoma to spread.
Staging
If you receive a diagnosis of melanoma, the next step is to determine the extent, or stage, of the cancer. Melanoma is staged using these criteria:
Melanoma is staged using the numbers 0 through IV:
The best treatment depends on your stage of cancer and your age, overall health and personal preferences. Typically, melanomas that haven't spread beyond the skin are surgically removed.
When melanoma has spread to another part of the body, options may include surgery, chemotherapy, radiation therapy, biological therapy, experimental therapy or a combination. It's important to understand the different treatments and their potential risks and side effects. Don't be afraid to discuss any questions you may have with your treatment team. You may also want to consider seeking a second opinion, especially from doctors who specialize in treating melanoma. In some cases, after weighing your options you may choose not to treat the melanoma itself but rather to try to relieve any symptoms the cancer may cause.
Treating early-stage melanomas
The best treatment for early-stage melanomas is surgical removal (simple excision). Very thin melanomas may have been entirely removed during the biopsy and require no further treatment. Otherwise, your surgeon will excise the cancer as well as a small border of normal skin and a layer of tissue beneath the skin. In almost every case this eliminates the cancer.
At one time, surgery for more invasive early-stage tumors involved cutting out the cancer along with a large border of normal skin (wide local excision). This usually meant having a skin graft — a procedure in which skin from another part of the body is used to replace the skin that's removed. But taking smaller amounts of normal skin in some cases of invasive melanomas may be just as effective in treating cancer and may eliminate the need for skin grafts.
Treating melanomas that have spread beyond the skin
The best news about melanoma is that many cases of skin cancer can be prevented simply by following these precautions:
Wear sunscreen year-round. Sunscreens don't filter out all harmful UV radiation, especially the radiation that can lead to melanoma. But they play a major role in an overall sun-protection program. Be sure to use a broad-spectrum sunscreen with a sun protection factor (SPF) of at least 15 when you go outside, year-round. Use a generous amount of sunscreen on all exposed skin, including your lips, the tips of your ears, and the backs of your hands and neck.
For the most protection, apply sunscreen 20 to 30 minutes before sun exposure and reapply it every two hours throughout the day, as well as after swimming or exercising. Apply sunscreen to young children before they go outdoors, and teach older children and teens how to use sunscreen to protect themselves. Keep a bottle of sunscreen in your car as well as with your gardening tools and sports and camping gear to remind yourself and your family to use it.
In July 2006, the Food and Drug Administration (FDA) approved a new over-the-counter sunscreen that will be marketed in the United States as Anthelios SX. The new sunscreen offers better protection from UVA rays than do traditional broad-spectrum sunscreens, according to the manufacturer. This may help reduce the risk of various types of skin cancer — including melanoma and basal and squamous cell carcinomas. Better UVA protection also may reduce sun-related skin wrinkling. But the added protection may come at a cost. Although U.S. prices aren't yet available, similar products sold in Canada cost about twice as much as traditional sunscreens — or even more.
Medical Articles describing appropriate protocall for 1mm biopsy Melanoma
| (1) | Department of Surgery, Turku University Hospital, P.O. Box 52, 20521 Turku, Finland |
| (2) | Department of Pathology, Turku University Hospital, Turku, Finland |
Received: 20 January 2005 Accepted: 28 June 2005 Published online: 29 July 2005
1 mm), the indication of SLNB is controversial since the risk of nodal metastasis is low. The aim of this study was to assess if SLNB detects occult nodal metastases among patients with thin melanomas.Melanomas that have not spread beyond the site at which they developed are highly curable. Most of these are thin lesions that have not invaded beyond the papillary dermis (Clark’s level I-II; Breslow thickness ≤1 mm). The treatment of localized melanoma is surgical excision with margins proportional to the microstage of the primary lesion; for most lesions 2 mm or less in thickness, this means 1 cm radial re-excision margins.[1,2]
Melanomas with a Breslow thickness of 2 mm or more are still curable in a significant proportion of patients, but the risk of lymph node and/or systemic metastasis increases with increasing thickness of the primary lesion. The local treatment for these melanomas is surgical excision with margins based on Breslow thickness and anatomic location. For most melanomas more than 2 mm to 4 mm in thickness, this means 2 cm to 3 cm radial excision margins. These patients should also be considered for sentinel lymph node biopsy followed by complete lymph node dissection if the sentinel node(s) are microscopically or macroscopically positive. Sentinel node biopsy should be performed prior to wide excision of the primary melanoma to ensure accurate lymphatic mapping. Patients with melanomas that have a Breslow thickness more than 4 mm should be considered for adjuvant therapy with high-dose interferon.
Some melanomas that have spread to regional lymph nodes may be curable with wide local excision of the primary tumor and removal of the involved regional lymph nodes.[3-6] In a prospective randomized controlled trial, adjuvant high-dose interferon was shown to increase relapse-free survival and overall survival (OS) when compared to observation.[7] A subsequent randomized trial conducted by the same group of investigators using the same high-dose interferon regimen confirmed the relapse-free survival but not the OS advantage.[8] A third randomized trial again demonstrated both a disease-free survival and OS advantage to high-dose interferon when compared to a ganglioside vaccine.[9] Clinicians should be aware that high-dose interferon regimens have substantial side effects, and patients should be monitored closely. Adjuvant therapy with lower doses of interferon have not been consistently shown to have an impact on either relapse-free survival or OS.[10] Adjuvant chemotherapy does not improve survival. A multicenter phase III randomized trial of patients with high-risk primary limb melanoma did not show a benefit from isolated limb perfusion with melphalan in regard to disease-free survival or OS when compared to surgery alone.[11]
Melanoma that has spread to distant sites is rarely curable with standard therapy, though high-dose interleukin-2 (IL-2) has been reported to produce durable responses in a small number of patients.[12,13] In patients with systemic metastasis confined to one anatomic site, long-term survival is occasionally achieved by complete resection of all metastatic disease.[14-17] All patients with distant metastasis are appropriately considered candidates for clinical trials exploring new forms of treatment, including combination chemotherapy, biological response modifiers (such as specific monoclonal antibodies, interferons, IL-2, or tumor necrosis factor-α), vaccine immunotherapy, or biochemotherapy (chemoimmunotherapy).
Malignant melanoma has been reported to spontaneously regress; however, the incidence of spontaneous complete regressions is less than 1%.[18]
Patients with all stages of melanoma may be considered candidates for ongoing clinical trials. Information about ongoing clinical trials is available from the NCI Web site.
The designations in PDQ that treatments are “standard†or “under clinical evaluation†are not to be used as a basis for reimbursement determinations.
What is melanoma? Can you explain my pathology report and tell me how serious my melanoma is? Breslow thickness: a measurement in millimeters (mm) of how deep the cancer has penetrated. One millimeter is approximately 1/25 inch. A thickness of less than 1.0 mm is considered a thin or early melanoma. Melanomas between 1.0 – 4.0 mm are generally considered intermediate thickness. Melanomas more than 4.0 mm are considered thick. Clark level: this is indicated by a Roman numeral from I-V. These numbers correspond to the different layers of the skin. Clark’s level I is the top layer (epidermis) of the skin, and melanomas confined to this layer are considered non-invasive and have not spread. Clark’s levels II-V are located in the dermis of the skin and are considered invasive with a tendency to spread. At level V, the melanoma has penetrated all the layers of the dermis into the subcutaneous fatty tissue. The Clark level is used for revised staging of patients with thin melanomas. What is the best treatment for primary melanoma? For melanomas 1mm or more in thickness, a larger area around the site is often removed. While many of these wider excisions can still be directly closed, in some cases a skin graft is necessary. Your surgeon will discuss this with you. Melanomas 1mm or more in thickness are considered somewhat more serious than thin melanomas, and may spread to nearby lymph nodes. A wide local excision is often done together with a sentinel lymph node biopsy to check for possible spread.
Melanoma is the most serious of the common skin cancers. The cancerous cells arise from melanocytes (nevi or mole cells), which gives your skin its color. Everyone has these pigment cells, but they can sometimes change, either spontaneously or when damaged by sun exposure. With time, this damage can result in cancer.
What causes melanoma?
Most melanomas are caused by sun damage. The greatest risk for developing melanoma probably comes from sunburns. People with fair skin or those who tend to burn easily are more at risk for sun damage as well as for melanoma. Other factors may also increase the risk, such as a genetic (inherited) tendency. There are rare types of melanomas that occur on places other than the skin, such as the lining of the inside of the eye, mouth, or rectum. Occasionally the site of origin of a melanoma in an individual patient cannot be found. In these melanomas, the cause is unknown.
Can you explain intra-operative lymphatic mapping and sentinel lymph node biopsy?
For patients with primary melanoma of the skin, the single most important part of the pathology report is the Breslow thickness. The likelihood that a person will be cured of melanoma after surgery is strongly related to this measurement. Your surgeon will recommend treatment based in part on your melanoma’s Breslow thickness as well as other factors:
The main treatment for primary melanoma is surgery. A thin melanoma is usually treated with a wide local excision of the skin. In this procedure, an area surrounding the melanoma site is removed. For thin melanomas, this area is usually 1cm, or about 3/8 inch. The excision is carried down through the fatty tissue to the covering over the muscle (the fascia). The incision is usually made so that the wound can be easily closed. In order to do this, the wound usually needs to be lengthened in one direction at least 3 times its maximum width. For example, a 1cm margin excision can result in a linear or curved scar at least 6cm (2.4 inches) in length.
This procedure is usually done at the same time as wide local excision for intermediate or thick melanomas. A small amount of radioactive material and blue dye is injected at the melanoma site. The lymphatic system picks up this tracer material and carries it to the lymph nodes close to the primary melanoma. These lymph nodes (called sentinel lymph nodes) are the ones most likely to contain cancer cells if the melanoma has metastasized (spread). The tracer will collect in one or more of these lymph nodes, which are then surgically removed through a small incision and examined under the microscope. The process of checking the lymph nodes for spread of melanoma can take up to two weeks.
After surgery, what is the next step?
For patients with thin melanomas who have a wide local excision alone, no further treatment is recommended if the pathology report is normal. Patients with successful surgical treatment for thin melanomas still need to be checked regularly with physical exams, lab work, and a chest
X-ray. Your melanoma health care team will discuss your follow-up schedule.
Patients with a wide local excision together with a negative sentinel lymph node biopsy (which showed no spread of melanoma) also generally need no further treatment. However, regular checkups are strongly recommended.
If you have a lymph node removed that indicates the melanoma has spread, your surgeon will recommend additional surgery to remove the rest of the lymph nodes in that area. This surgery is called lymphadenectomy or lymph node dissection. In addition, patients with spread of melanoma to lymph nodes sometimes take additional treatments (adjuvant therapy) after recovery from surgery to help prevent recurrence or further spread. These treatments can include medications, such as interferon-alpha; vaccine treatments; chemotherapy; or radiation therapy. Your health care team will discuss these options with you when indicated.
When will my surgery be scheduled?
Most procedures are scheduled within two to four weeks of your first clinic visit. It will not be done the same day as your first visit with your surgeon, but it will be scheduled in a timely manner. Please be aware that other patients are awaiting surgery as well. Your surgeon will not put your health in danger by postponing surgery.
How long will I need to be in the hospital for my surgery?
If you are having a wide local excision, this will be an outpatient procedure and you can go home the same day. This procedure is performed under local anesthesia. Sometimes, medications to relax you (sedation) are given through an IV tube.
If you are having a wide local excision with intra-operative lymphatic mapping and sentinel lymph node biopsy, you may stay in the hospital overnight. This surgery often is done under general anesthesia. If you have no side effects from the anesthesia and are feeling well, you may go home the same day.
If you are having an axillary lymph node dissection, which is done under general anesthesia, you will stay overnight.
If you are having a groin (or inguinal) lymph node dissection, you will stay in the hospital at least 3 days. This surgery is done under general anesthesia.
After surgery, you will be instructed on how to care for your incision. You will get an appointment to return to the Melanoma and Skin Center for a wound check, for drain or suture removal (if necessary), to discuss the results of your final pathology report, and make plans for any additional care. Most patients return to the Center about 1-4 weeks following surgery.
What about my other skin lesions?
People who develop one melanoma are at risk for developing additional melanomas. During your first visit, your skin will be checked for other suspicious lesions. If any look suspicious, a biopsy will be performed. Once you are diagnosed with melanoma, it's important that you become familiar with your skin to get a good idea of what your existing lesions look like. Every time you come for a check-up, we will examine your skin as well as your surgery site. However, you should still perform monthly skin self-exams. There are 5 things to check for, called the ABCDEs of melanoma.
What are the ABCDEs of melanoma?
Asymmetry. Look for lesions that look different when one side is compared to the other. If you draw a line down the center of the lesion, do the two sides look the same?
Border. Look at the edges of the lesion. Are the borders smooth or jagged?
Color. Look for changes in the color of the lesion. Is it getting darker, is part of it changing color, or does it contain several different colors?
Diameter. Look at the size of the lesion. Is it more than 6 mm in diameter (the size of a pencil eraser)?
Elevation. Look for signs of the lesion becoming raised. Is it growing in height?
How can I prevent future melanomas?
Risk of developing melanoma is related in part to sun damage. Prior sun exposure, a natural tendency to develop melanomas, or both, can sometimes cause melanoma patients to develop a separate, new melanoma elsewhere on their body. You cannot necessarily prevent this from happening. However, with regular skin self-exams, you may be able to identify suspicious moles in a very early stage. Individuals who have had melanoma should also limit their sun exposure. It is most important to avoid sunburn. We recommend that you limit your sun exposure during the peak periods of ultraviolet light exposure (10:00 a.m.-3:00 p.m.). When outdoors, wear a sunscreen rated at least SPF 30, a broad brimmed hat and a long-sleeved shirt. You may also consider special sun protective clothing.
We also recommend you practice monthly self-skin examinations, and that you keep all of your follow-up appointments with your melanoma health care team and your dermatologist.

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©2007 The University of Texas M. D. Anderson Cancer Center |