Skin cancer is a group of malignant skin tumours that develop when skin cells begin to divide uncontrollably and form a tumour. It is not one specific tumour and does not refer only to melanoma. The most common types of skin cancer are basal cell carcinoma, also known as basalioma, squamous cell carcinoma and melanoma. Less common malignant skin tumours include Merkel cell carcinoma, cutaneous lymphomas, Kaposi sarcoma and other tumours.
Skin cancer can have many different appearances. It may resemble a mole, but in other cases it can appear as a pale, pink, skin-coloured, rough, scaly, bleeding or non-healing skin lesion. It is therefore important to recognise not only the signs of melanoma but also the possible manifestations of non-melanoma skin cancer, particularly basal cell carcinoma and squamous cell carcinoma.
Skin cancer is often associated with prolonged or intense exposure to ultraviolet radiation. The main sources of UV radiation are sunlight and artificial UV sources such as sunbeds. The risk is higher in people with fair skin, frequent sunburn, numerous moles, a weakened immune system, a family history of skin cancer or a previous skin cancer diagnosis. However, skin cancer can also develop in people without obvious risk factors and on skin that previously appeared completely normal.
The positive aspect is that some skin cancers can be detected early because they develop on the surface of the skin and may be visible. Early diagnosis substantially improves treatment options, reduces the risk of tissue damage and, in melanoma, can be decisive for the prognosis.
Skin cancer is a malignant tumour that develops from different types of skin cells. The skin consists of several layers and multiple cell types. The type of skin cancer that develops depends on which cells become malignant.
Basal cell carcinoma develops from basal cells located in the deepest part of the outer layer of the skin, known as the epidermis. Squamous cell carcinoma develops from squamous cells that form the upper layers of the epidermis. Melanoma develops from melanocytes, the pigment-producing cells that create melanin and give colour to the skin, hair and moles. Merkel cell carcinoma is a rare and aggressive form of skin cancer whose tumour cells display neuroendocrine characteristics.
Skin cancer is not always melanoma. In fact, most skin cancers belong to the non-melanoma skin cancer group. This group most commonly includes basal cell carcinoma and squamous cell carcinoma. Melanoma is less common but is generally more dangerous because, when not detected early, it has a greater risk of spreading to the lymph nodes and other organs.
Understanding the different types of skin cancer is important because they vary in appearance, growth rate, risk of spreading and treatment approach. This article provides an overview, while detailed information about each diagnosis is available in separate Medart encyclopaedia articles.
Basal cell carcinoma is the most common type of skin cancer. It usually grows slowly and most often develops on sun-exposed areas such as the face, nose, forehead, ears, neck or scalp. It may appear as a non-healing ulcer, a pearly or shiny nodule, a pink patch, a repeatedly bleeding skin lesion or a scab that does not disappear.
Basal cell carcinoma usually has a low risk of metastasis, but it is nevertheless a malignant tumour. If left untreated, it can locally damage the skin, cartilage, bone and surrounding tissues, particularly when located on the nose, ears, eyelids or other anatomically complex areas.
Squamous cell carcinoma is a skin cancer that develops from squamous skin cells. It frequently develops on sun-damaged skin but can also arise in chronic wounds, scars or areas of persistent inflammation. It may appear as a rough, scaly, thickened or painful lesion, an ulcer, a crust or a bleeding area of skin.
Squamous cell carcinoma has a greater risk of spreading than basal cell carcinoma, particularly when the tumour is located on the lips, ears, scars or chronic wounds, or when the person has a weakened immune system. Suspicious rough, scaly or bleeding skin lesions should therefore be assessed without unnecessary delay.
Melanoma is a skin cancer that develops from pigment-producing cells known as melanocytes. It may arise from an existing mole but can also appear as a new lesion on previously normal skin. Melanoma is often associated with a dark or multicoloured mole, although it is not always black. Some melanomas may be pink, red or pale.
Melanoma is less common than basal cell carcinoma and squamous cell carcinoma, but it is particularly important because it has a greater risk of spreading if it is not detected early. Suspicious signs include asymmetry, irregular borders, multiple colours, enlargement and any change over time.
Actinic keratosis is not yet an invasive skin cancer, but it is a precancerous change caused by sun damage that may, in some cases, progress to squamous cell carcinoma. It usually appears as a rough, scaly, dry, pink or brownish patch on sun-exposed skin, including the face, forehead, nose, ears, scalp, hands or forearms.
Actinic keratosis is important because some lesions may develop into squamous cell carcinoma. It should not be regarded merely as “dry skin” or a cosmetic concern. A rough patch that does not disappear, repeatedly returns or becomes tender should be examined by a dermatologist.
Merkel cell carcinoma is a rare but aggressive form of skin cancer. It may appear as a rapidly growing, usually painless pink, red, bluish or purple nodule. It occurs more commonly in older adults, on sun-damaged skin and in people with a weakened immune system.
Although Merkel cell carcinoma is much less common than melanoma, basal cell carcinoma or squamous cell carcinoma, it is medically important because it can grow and spread rapidly. Such a lesion requires prompt medical assessment.
Non-melanoma skin cancer is a general term for skin cancers other than melanoma. It most commonly refers to basal cell carcinoma and squamous cell carcinoma. These tumours generally develop from keratinocytes, the main cells of the epidermis, and are therefore also known as keratinocyte carcinomas.
Basal cell carcinoma and squamous cell carcinoma most frequently develop on sun-exposed areas such as the face, nose, ears, lips, scalp, neck, hands and forearms. However, they may also occur elsewhere. Basal cell carcinoma generally grows slowly and rarely metastasises, but it can cause substantial local tissue damage if left untreated. Squamous cell carcinoma can be more aggressive and may, in some cases, spread to the lymph nodes or other organs.
Skin cancer is not an infection. It cannot be transmitted from one person to another through touching the skin, sharing towels, swimming in a pool or ordinary everyday contact. It is therefore more accurate to refer to the mechanism of skin cancer development rather than a mechanism of infection.
Skin cancer develops when damage accumulates in the genetic material, or DNA, of skin cells. DNA acts as the cell’s instruction system, determining when the cell should divide, stop dividing and die. If DNA damage affects the mechanisms controlling cell growth, cells may begin to divide uncontrollably. Over time, these cells can form a malignant tumour.
Ultraviolet radiation is one of the most important causes of DNA damage. UV radiation can directly damage cellular DNA and promote the accumulation of mutations. The body has DNA-repair mechanisms and immune surveillance that help identify and eliminate damaged cells. However, when damage is extensive, repeated over many years or accompanied by a weakened immune system, the risk of a malignant tumour increases.
Genetic predisposition, skin type, previous sunburn, chronic wounds, scars, exposure to certain chemicals, immunosuppression and a previous skin cancer diagnosis may also contribute to the development of skin cancer. In melanoma, the number of moles and the presence of atypical moles are also relevant.
Skin cancer does not usually develop within a single day. In most cases, it is a long-term process in which cellular damage accumulates gradually. The patient usually notices only the visible stage, such as a new lesion, a changing mole, a non-healing wound or a bleeding area of skin.
DNA damage develops in skin cells. The skin may still look normal, or signs of sun damage such as pigmentation, wrinkles and roughness may appear.
Some damaged cells are repaired or destroyed, while others retain mutations. Actinic keratosis, new skin patches or changing lesions may appear.
Cells become atypical, but invasive cancer has not yet developed. A person may notice a persistent rough or scaly patch, particularly on the face, ears, scalp or hands.
A malignant tumour develops within the superficial layers of the skin. It may appear as a non-healing ulcer, pearly nodule, pink patch, changing mole, bleeding lesion or persistent crust.
The tumour may grow deeper, damage surrounding tissues or spread. The lesion may enlarge, become painful, bleed, ulcerate or thicken, and enlarged lymph nodes may appear.
Skin cancer symptoms are not identical in every patient. Different tumours may have different appearances, and the lesion may initially seem insignificant. It is particularly important to notice changes over time: a lesion may grow, change colour, bleed, fail to heal, itch, become painful or look different from a person’s other skin lesions.
A dermatologist should assess the skin if any of the following signs are present:
For practical purposes, it is helpful to remember several signs that should not be observed at home for a prolonged period without medical assessment.
Basal cell carcinoma and squamous cell carcinoma may present as a skin lesion that does not heal or repeatedly forms a crust.
Repeated bleeding without a clear cause may indicate a malignant or precancerous process.
Changes in size, shape, colour, borders or sensation are important warning signs of melanoma.
This may be a sign of actinic keratosis or squamous cell carcinoma, particularly on sun-exposed skin.
The “ugly duckling” principle helps identify a lesion that does not match the usual pattern of a person’s moles or skin lesions.
Skin cancer may be painless and cause no symptoms at first. This is one reason why people sometimes delay seeing a doctor. However, skin cancer may also itch, tingle, become tender or painful, bleed or repeatedly form a crust. The absence of symptoms does not mean that a lesion is safe, and pain alone does not mean that it is cancer. The appearance of the lesion, changes over time and medical assessment are the most important factors.
No. Melanoma may often be dark or multicoloured, but this is not always the case. Some melanomas are pink, red or pale. Basal cell carcinoma and squamous cell carcinoma are often not dark and may appear pink, skin-coloured, pearly, scaly, ulcerated or similar to a non-healing wound. Skin cancer should therefore not be associated only with a black mole.
Skin cancer develops more commonly on areas that have received substantial UV exposure over a lifetime. Typical locations include the face, nose, ears, lips, forehead, scalp, neck, shoulders, back, chest, hands, forearms and lower legs.
However, skin cancer can also occur in areas that receive little sunlight. Melanoma may develop on the soles, palms, beneath the nails, on mucous membranes or in other less visible locations. A skin self-examination should therefore include not only the face and hands, but also the back, scalp, feet, spaces between the toes, nails and skin folds.
Melanoma may develop from an existing mole, but it can also arise as a completely new lesion on previously normal skin. It is therefore important to monitor not only existing moles but also new pigmented or unusual lesions.
The ABCDE principle is widely used when assessing moles:
Another practical principle is the “ugly duckling” sign. It means that attention should be paid to a lesion that looks different from a person’s other moles. If most moles are similar but one is noticeably darker, larger, more irregular or otherwise different, it should be examined by a dermatologist.
Detailed information about melanoma signs is available in the article “Melanoma”. Practical information about mole assessment is available in “Mole examination”. Information about examination using a specialised optical instrument is available in “Dermoscopy”.
The risk of skin cancer increases when a person is repeatedly or chronically exposed to UV radiation and when the body has a reduced ability to repair or eliminate damaged cells. Risk is not the same for everyone but may be increased in the following situations:
Fair skin increases the risk because it contains less melanin, a pigment that provides partial protection from UV radiation. However, skin cancer can also occur in people with darker skin and may be diagnosed later if it is not recognised promptly.
Most cases of skin cancer are not directly inherited in a simple manner. However, risk-related characteristics may run in families, including skin type, the number of moles, a tendency to develop atypical moles or certain genetic mutations. If a first-degree relative has had melanoma or several family members have had skin cancer, individual risk should be discussed with a dermatologist.
The body does not develop immunity to skin cancer in the way it may develop protection against certain infections following illness or vaccination. A person cannot “recover from” skin cancer and become protected from developing it in the future. On the contrary, a person who has previously had skin cancer may have an increased lifetime risk of developing another skin cancer.
The immune system nevertheless plays an important role in tumour surveillance. A healthy immune system can recognise and destroy some damaged or atypical cells. When the immune system is suppressed, for example after organ transplantation or because of certain treatments, the risk of squamous cell carcinoma and other skin tumours may be increased. Modern oncology also uses the immune system’s ability to recognise cancer cells: in some advanced skin cancers, a doctor may prescribe an immunotherapy-type treatment.
You should consult a dermatologist if a skin lesion is new, changing, non-healing, bleeding, itchy, painful, rapidly growing or looks different from other lesions. Medical assessment should not be delayed if the lesion is located on the face, nose, ears, lips, scalp, genital area, sole or beneath a nail, or if the patient has previously had skin cancer.
A medical consultation is also advisable for people with numerous or atypical moles, a family history of melanoma, repeated sunburn or regular sunbed exposure. In higher-risk patients, the dermatologist may recommend regular preventive skin examinations.
The diagnosis of skin cancer begins with a dermatological examination. The doctor assesses the lesion’s appearance, location, size, colour, borders, surface, symptoms and changes over time. Information about previous sunburn, sunbed use, family history, previous skin tumours and immune status is also important.
Dermoscopy is the examination of a skin lesion using a specialised instrument known as a dermatoscope. It allows the doctor to assess structures under magnification that cannot be seen with the naked eye. Dermoscopy helps distinguish benign lesions from suspicious ones, but a final cancer diagnosis is usually confirmed by histological examination.
If a lesion is suspicious, the doctor may recommend a biopsy or surgical removal. A biopsy involves taking a tissue sample for laboratory analysis. Histological examination means examining the tissue under a microscope to determine whether malignant cells are present, identify the tumour type and assess other features important for treatment.
Not every skin lesion needs to be removed. Some benign lesions can be monitored, while others may be removed for cosmetic or mechanical reasons. Suspicious lesions, however, must be examined using a medically appropriate method. If melanoma is suspected, the removal method must be selected particularly carefully so that accurate histological assessment is not compromised.
An experienced dermatologist can often assess whether a lesion appears benign, suspicious or highly suspicious. However, the final diagnosis frequently depends on histology. This means that the doctor may have a well-founded clinical suspicion of skin cancer, but laboratory examination of the tissue is required for confirmation.
There is no single universal examination interval suitable for everyone. The frequency of checks is determined according to individual risk. People with numerous moles, atypical moles, a family history of melanoma, previous skin cancer, fair skin, immunosuppression or significant UV exposure may be advised by a dermatologist to attend regular examinations at defined intervals.
Regardless of the scheduled preventive examination, medical advice should be sought sooner if a new, changing, bleeding, rapidly growing or non-healing lesion appears.
Skin cancer treatment depends on the tumour type, size, depth, location, histological characteristics, the patient’s age and general health, and whether the tumour is localised or has spread. The treatment plan is determined by a doctor, often in cooperation with a dermatologist, surgeon, oncologist or other specialists.
Main treatment approaches may include:
Specific prescription medicines are not listed in this article because treatment selection is individual and must be determined by a doctor after assessing the diagnosis, histology, stage and the patient’s overall health.
Many skin cancers detected at an early stage can be treated successfully. The prognosis for basal cell carcinoma is generally favourable when it is diagnosed and treated promptly, although an untreated tumour may cause substantial damage to surrounding tissues. The prognosis for squamous cell carcinoma depends on the tumour’s size, depth, location and risk features. The prognosis for melanoma largely depends on how deeply the tumour has grown into the skin and whether it has spread.
The earlier skin cancer is detected, the greater the possibility of treating it with a smaller intervention and achieving a better outcome. A person should not wait until a lesion becomes large, painful or obviously dangerous.
Surgery is a very common and effective treatment for skin cancer, but it is not always the only option. In selected cases, particularly for superficial lesions or precancerous changes, the doctor may choose another method. However, when invasive skin cancer or melanoma is suspected, histological assessment of the tissue is essential, and the treatment method must be selected so that diagnostic accuracy and patient safety are not compromised.
Certain superficial skin changes and precancerous lesions can sometimes be treated using local methods, including prescription medicines or procedures selected by a doctor. However, lasers and creams are not universal treatments for skin cancer. Attempting to burn, dissolve or remove a suspicious lesion without medical supervision can delay diagnosis and interfere with histological examination.
A scar usually remains after surgical removal of a skin lesion because the skin is cut and must heal. The size and appearance of the scar depend on the lesion’s size and location, the selected method, individual healing characteristics and postoperative care. The doctor’s aim is to treat the tumour fully while preserving function and achieving the best possible cosmetic result, particularly on the face and other visible areas.
Yes. Skin cancer can recur, particularly if the tumour was high-risk, located in an anatomically difficult area or could not be removed completely. In addition, a person who has previously had skin cancer may have an increased risk of developing a new skin cancer elsewhere. Follow-up appointments and regular skin self-examination are therefore important after treatment.
The degree of risk varies substantially between different types of skin cancer. Basal cell carcinoma usually grows slowly and rarely spreads but can cause significant local tissue damage. Squamous cell carcinoma can be more aggressive and may metastasise in certain cases. Melanoma is particularly dangerous when diagnosed late because it can spread to the lymph nodes and other organs. Merkel cell carcinoma is rare but is an aggressive form of skin cancer.
Skin cancer can be fatal, particularly in late-stage melanoma, advanced squamous cell carcinoma or Merkel cell carcinoma. However, skin cancer detected at an early stage can often be treated successfully. Early recognition, accurate diagnosis and timely treatment are therefore essential.
Untreated skin cancer may continue to grow. Basal cell carcinoma may invade more deeply and damage surrounding tissues, particularly on the nose, ears, eyelids and other anatomically complex areas. Squamous cell carcinoma may enlarge, ulcerate, become painful and, in some cases, spread to the lymph nodes. Untreated melanoma may spread through the body and become life-threatening. A suspicious lesion should therefore not be observed for a prolonged period without medical assessment.
The risk of skin cancer cannot be reduced to zero, but it can be substantially lowered by limiting UV-related skin damage and arranging prompt assessment of suspicious lesions.
Main preventive measures include:
A sunscreen should provide broad-spectrum protection, meaning protection against both UVA and UVB radiation. A sufficiently high SPF should be used in daily life and particularly during summer. For people with a high risk, fair skin, previous skin tumours or intense sun exposure, a doctor may recommend SPF 50+ protection. Sunscreen should not be treated as permission to remain in the sun longer but as one part of combined protection that also includes shade, protective clothing and limiting excessive UV exposure.
Yes. UV radiation can reach the skin even when the weather is cloudy. Clouds reduce visible sunlight but do not always reduce UV exposure sufficiently. Sun protection remains important during prolonged outdoor activity, particularly in spring and summer, even when the sun is not directly visible.
Sunbeds are not a safe way to achieve a “healthy tan” and do not prevent skin cancer. Artificial UV radiation damages the DNA of skin cells and increases the risk of skin cancer. Even occasional sunbed use cannot be considered safe, particularly for people with fair skin, numerous moles, a family history of melanoma or previous sunburn.
Skin self-examination helps identify new or changing lesions. It should be performed in good lighting, using a mirror or asking another person to help examine areas that are difficult to see.
During a self-examination, check:
It is particularly important to monitor changes over time. A suspicious lesion may be photographed under similar conditions for comparison, but a photograph does not replace a medical examination.
Yes. Children’s skin is sensitive to sunburn, and sunburn during childhood may increase the risk of skin cancer later in life. Shade, appropriate clothing, a hat, sunglasses and age-appropriate sunscreen are important for children. Babies and young children should be protected particularly carefully from direct sunlight.
Protection from UV radiation becomes especially important after a skin cancer diagnosis. This does not mean that a person cannot go outdoors, but deliberate tanning, sunbeds and sunburn should be avoided. A doctor can provide individual recommendations based on the type of skin cancer, treatment and future risk.
It is well established that UV radiation from the sun and sunbeds is an important risk factor for skin cancer. The importance of early diagnosis is also strongly supported: the earlier a suspicious lesion is assessed and treated, the better the treatment options usually are.
Dermoscopy is an important dermatological diagnostic method that helps assess skin lesions more accurately. Histological examination remains the main method for confirming a diagnosis of skin cancer.
Several innovations are developing in the field of skin cancer. These include digital dermoscopy, total-body skin mapping, artificial-intelligence-supported image analysis and personalised risk assessment. Artificial intelligence may help identify suspicious lesions, but it does not replace a dermatologist because diagnosis requires clinical context and often histological examination.
In oncology, immunotherapy and targeted-therapy approaches continue to develop for advanced melanoma, high-risk squamous cell carcinoma and other aggressive skin tumours. Researchers are also seeking better ways to distinguish low-risk lesions from those requiring rapid and more intensive treatment, with the aim of improving patient safety while avoiding unnecessary procedures.
The information provided in this article is intended for informational and educational purposes only and does not replace medical consultation, diagnosis or treatment. Self-assessment of skin lesions can be inaccurate because skin cancer may resemble a benign lesion, while benign lesions may sometimes appear suspicious. If you notice a new, changing, bleeding, painful, itchy, non-healing or otherwise suspicious skin lesion, consult a dermatologist, dermato-oncologist or another appropriate specialist. Do not attempt to treat, burn, cut or remove suspicious lesions yourself. If symptoms deteriorate rapidly, the lesion grows quickly, bleeds heavily, causes severe pain, develops purulent inflammation or is accompanied by enlarged lymph nodes, urgent medical assessment is required.
Skin cancer is a group of malignant skin tumours that develop when skin cells begin to grow uncontrollably.
No. The most common types are basal cell carcinoma, squamous cell carcinoma and melanoma.
The main types are basal cell carcinoma, squamous cell carcinoma, melanoma and, less commonly, Merkel cell carcinoma.
It is skin cancer that is not melanoma. Most commonly it is basal cell carcinoma or squamous cell carcinoma.
The most common is basal cell carcinoma.
Of the most common types, melanoma is generally the most dangerous, as it can spread throughout the body.
It may appear as a non-healing sore, a pink spot, a rough patch, a nodule or a changing mole.
No. Skin cancer can also be pink, red, skin-coloured, pearly or scaly.
Not always. It may not cause pain, but can also become tender, painful or inflamed.
Yes, skin cancer can sometimes itch, but itching alone is not a specific sign of cancer.
Yes. Repeated bleeding from a skin lesion is a sign that should be checked by a dermatologist.
Yes. A non-healing sore or wound can be a sign of basal cell carcinoma or squamous cell carcinoma.
It is a principle for evaluating moles: asymmetry, border, colour, diameter and evolution.
It is a lesion that looks different from the person's other moles or skin lesions.
No. Melanoma can develop both from an existing mole and on previously normal skin.
Yes. The face, nose, ears and lips are common locations for skin cancer.
Yes. Melanoma can also appear under a nail as a dark streak or a changing pigmented area.
A significant cause is DNA damage caused by UV radiation, but genetics, immunity and other factors also play a role.
Yes. The artificial UV radiation from sunbeds damages the skin and increases the risk of skin cancer.
People with fair skin, sunburn history, many moles, a family history, weakened immunity or a previous skin cancer.
Through a dermatologist's examination, dermoscopy and, if necessary, biopsy or excision with histology.
Dermoscopy is the examination of a skin lesion under magnification using a specialised device.
A biopsy is needed when the doctor considers the lesion to be suspicious and tissue examination under a microscope is required.
Skin cancer detected early can often be treated successfully.
Treatment may include surgery, local methods, radiation therapy, immunotherapy or targeted therapy.
Only in certain cases and with prescription medicines prescribed by a doctor. Self-treatment is not safe.
A scar usually remains after surgical removal, but the doctor chooses the method to achieve a safe and aesthetically acceptable result.
Yes. It can recur or a new skin cancer can develop in another location.
Limit UV exposure, avoid sunbeds, use sun protection and have your skin checked regularly.
If a lesion changes, grows, bleeds, does not heal, itches, hurts or looks different from the others.
| Qualification | Clients of the clinic | First visit |
|---|---|---|
| Doctor | 45 € | 55 € |
| Highly qualified doctor | 52.25 € | 55 € |
| Dr. Med. | 66.50 € | 70 € |
The final price of a skin lesion examination consists of the consultation fee and the fee for each additional skin lesion examined dermatoscopically, if more than one skin lesion is examined (please note that the consultation fee depends on the doctor’s qualification).
An in-depth examination with a dermatoscope is offered only for medium-risk and high-risk lesions.
For example, if during the consultation a dermatologist (doctor’s consultation fee — 55 €) observes two suspicious skin lesions, and the patient agrees to have both skin lesions examined with a dermatoscope (examination of the first skin lesion is included in the consultation fee + 10 € for each additional one), the total cost of the consultation will be 65 € (55 € + 10 €).
| Doctor’s qualification | Consultation fee |
|---|---|
| Doctor | 55 € |
| Highly qualified doctor | 55 € |
| Dr. med. | 70 € |
| Procedure | Price per item |
|---|---|
| Examination of one skin lesion | included in the consultation fee |
| For each additional one | 10 € |
Dermatologist Dr. Med. assistant professor Māra Rone-KupfereAsk a question Make an appointment |
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Dermatologist Dr. med. Dace BuileAsk a question Make an appointment |







