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Malignant skin tumours are among the most common types of cancer; in most cases they develop on areas of skin exposed to the sun (insolation). The disease is common among people who work outdoors, athletes and people who overindulge in sunbathing; its incidence is inversely related to the melanin content of the skin, and patients with a fair skin type are at the greatest risk. Malignant skin tumours may also develop years after exposure to sunlight or contact with carcinogens (for example, after ingesting arsenic).
As a rule, the disease is asymptomatic at first. The most common sign is a red or pigmented lesion with irregular outlines that does not go away. Any growing lesion should be excised and examined histologically — regardless of whether it is painful or inflamed, crusted or has bled. Treated early, skin cancer is curable in most cases.
Thorough diagnostics are the cornerstone of treatment. Highly professional clinical expertise becomes the most important part of the work-up. It is particularly valuable in dermatology, which demands considerable diagnostic experience of the specialist — yet at times even that is not enough.
From surgery to remove the tumour through to drug therapy and radiotherapy — specialised centres offer every melanoma treatment method currently available anywhere in the world. Patients also have access to new options within clinical trials. Where necessary, dermato-oncologists coordinate treatment with other specialist departments. Every patient's case is discussed at a weekly multidisciplinary conference, and the most suitable therapy is chosen on an interdisciplinary basis according to evidence-based criteria. If required, metastases in other organs are operated on in the surgical departments, radiotherapy is delivered by the radiology department, and pain syndromes are managed in the outpatient clinic.
Basalioma — basal cell carcinoma — is the most common type of skin cancer. It develops most often in people with fair skin and a history of sun exposure, and only very rarely in people with dark, pigmented skin.
A superficial, slow-growing papule or nodule arises from cells of the epidermis — basaloid keratinocytes. Metastases are rare, but local growth may be accompanied by marked tissue destruction. The diagnosis is established by histological examination. Treatment depends on the characteristics of the lesion and may involve:
The clinical picture and biological behaviour of basaliomas are extremely variable. They may appear as:
Basal cell carcinomas usually present as shiny, slow-growing papules that, after several months or years, acquire a border of shiny, pearl-like papules with dilated, blood-filled vessels (telangiectasias) on the surface and a central depression or ulcer. Recurrent crusting or bleeding is not typical.
Basaliomas rarely metastasise, but they can invade healthy tissue. Occasionally people die because of damage to vital structures (for example, the eyes, ears, oral cavity, bones or dura mater)or orifices as the tumour grows into tissues and organs.
Almost 25% of patients with a history of basalioma develop a new one within 5 years of the first; they should have an annual examination by a dermatologist.
Local treatment is indicated. The clinical picture, size, location and histological subtype determine the choice of strategy – curettage and electrocoagulation, surgical removal of the lesion, cryotherapy, chemotherapy with topical agents (imiquimod or 5-fluorouracil) and photodynamic therapy, or sometimes radiotherapy.
For recurrent, incompletely removed or large lesions, for sites prone to recurrence (for example, on the head or neck) and for the morphoeaform type of basalioma with indistinct margins, excision with microscopic margin control according to Mohs is often performed, in which the margins of the wound are excised step by step until the tissue samples are free of malignant cells
(rapid analysis under the microscope during the excision procedure).
In metastatic or locally advanced tumours, surgery or radiotherapy may not be feasible (for example, because of extensive involvement, recurrence or metastasis); here the indicated treatment is vismodegib (Vismodegib)). The drug vismodegib, developed by Roche, , has proven itself well in advanced basal cell carcinoma. Vismodegib inhibits the “hedgehog” signalling pathway, blocking the development of cancer cells. As a result of vismodegib treatment the size of the tumour is significantly reduced and visible lesions heal in patients with locally advanced and with metastatic BCC.
Besides excessive sun exposure, which is the main risk factor for skin cancer, there are others:
skin phototype I: fair skin with freckles, red or blond hair, light-coloured eyes;
age > 50 years;
living in an area with high levels of solar radiation;
sunburn in the past;
precancerous skin conditions (actinic keratosis);
a history of skin cancer;
skin cancer in close relatives.
In recent decades a steady rise has been recorded worldwide in the incidence of non-melanoma skin cancers, which include basal cell and squamous cell carcinoma. Actinic keratosis is biologically regarded as a “precancerous condition” and, on histological examination, may prove to be an early squamous cell carcinoma.
Routine screening for skin cancer is carried out by the patient through self-examination of the skin in a mirror, by the doctor during an examination, or by both.
Since many forms of skin cancer appear to be linked to ultraviolet (UV) exposure, a number of measures are recommended to reduce the harmful effect of the sun on the skin. You should:
avoid sun exposure: stay in the shade, keep outdoor activity to a minimum between 10 a.m. and 4 p.m. (when the sun's rays are strongest), and avoid sunbathing and the use of tanning beds;
wear protective clothing (long-sleeved shirts, trousers and wide-brimmed hats);
use sunscreens with a sun protection factor (SPF) of 30 or higher and broad-spectrum UVA/UVB protection, and apply them as instructed (that is, reapply every 2 hours or after swimming or sweating);
sunscreens must not be used as a way of prolonging time spent in the sun.
The data currently available are insufficient to assess the effect of these measures on the incidence of and mortality from melanoma; in non-melanoma skin cancers (basal cell carcinoma and squamous cell carcinoma) sun protection measures do reduce the number of new cases.
The treatment of actinic keratosis and “non-melanoma” skin cancer is a highly topical issue: incidence is high, the disease tends to recur, lesions are frequently located on exposed areas of skin and especially on the face, existing treatments are not effective enough, and they leave significant cosmetic defects. One of the most effective and gentlest treatments for “non-melanoma” skin cancer is photodynamic therapy.
Photodynamic therapy (PDT) is an effective non-invasive treatment for skin cancer, based on the selective accumulation of a photosensitising agent in tumour cells and their subsequent photodynamic destruction through chemical reactions triggered by light of a particular spectrum.
The key component of this reaction is the photosensitiser (PS) - a substance that increases the sensitivity of diseased tissue to light: the tumour or affected tissue is destroyed when it is irradiated with low-intensity light. Using a photosensitiser rules out the risk of uncontrolled thermal damage to tissues and organs and effectively destroys the altered areas of skin while preserving the surrounding healthy tissue as far as possible.
For photodynamic therapy, Metvix® cream is used as the topical photosensitiser, together with the unique Aktilite® photodynamic lamp. The lamp emits cold visible light in the red part of the spectrum. Applying Metvix® cream leads to a selective increase in the porphyrin content of tumour cells. These photoactive particles make the tumour cells sensitive to light. In healthy cells the porphyrin content is very low. Once the cell membranes and altered tissues have been activated by the photosensitiser, they are bombarded with light particles and completely destroyed. The replacement of the dead tumour cells by healthy ones gives an excellent cosmetic result. Photodynamic therapy with Metvix® is therefore a world-leading option for the treatment and long-term management of patients with “non-melanoma” types of skin cancer and actinic keratosis.
actinic keratosis of the face and scalp;
superficial and/or nodular basal cell skin cancer (cutaneous basalioma);
squamous cell carcinoma of the skin in situ (Bowen's disease).
hypersensitivity to the components of the preparation;
morphoeaform basal cell skin cancer;
porphyria;
allergic reactions to peanut oil;
pregnancy.
preparation stage: anaesthesia, mechanical cleansing of the lesion, removal of scales and crusts;
application of Metvix cream; the treated area is covered with an occlusive dressing for 3 hours;
light exposure: irradiation lasts 7-10 minutes.
The effect of treatment should be assessed 3 months after the procedure.
Actinic keratosis is treated with a single session of photodynamic therapy. Three months later the result of treatment is assessed and, if necessary, a second session is carried out.
Basalioma and Bowen's disease require two sessions with an interval of 7 days between them.
Photodynamic therapy is a unique method of treating skin cancer that has a great many advantages:
non-invasive treatment of the tumour-affected area of skin only;
treatment of skin cancer in areas that are difficult to reach surgically (the nose, the ears);
photodynamic therapy (PDT) can be repeated many times;
treatment is possible for elderly patients and for patients with severe comorbidities;
treatment can be given on an outpatient basis;
several lesions can be treated in a single session.
Its selective anti-tumour action sets photodynamic therapy (PDT) apart from the conventional treatments used in cancer patients.
Photodynamic anti-tumour therapy (PDT) compares favourably with conventional treatments because of its selective action. It is a local chemotherapy that is activated by light. The mechanism of PDT is that the light-sensitive substance accumulates specifically in cancer cells and, under light quanta of a particular wavelength, photochemical reactions take place that lead to the death of the tumour cells
In the treatment of disseminated melanoma and basal cell carcinoma, PDT has proved excellent thanks to its ability to destroy the tumour completely with minimal damage to the surrounding healthy tissue, the preservation of organ function, the option of repeat sessions and good cosmetic results.
It may be indicated for tumours in awkward locations (the corner of the eye, the ear, the ala of the nose, the nasolabial fold and so on), as well as for tumours that are resistant to conventional treatment.
urgent arrangement of an appointment with leading German oncology experts;
diagnosis and treatment exclusively at certified university cancer centres;
innovative diagnostic techniques;
accurate pathological diagnosis at certified institutes of pathology;
treatment starting without delay once the work-up is complete;
selection of the optimal individual therapy by a multidisciplinary tumour board (surgeons, dermatologists, radiologists, haematologists, chemotherapists, pathologists and nuclear medicine specialists);
adherence to international treatment protocols;
innovative methods of treating cancer;
non-invasive treatment of the tumour-affected area of skin only;
the use of minimally invasive surgical techniques wherever possible;
implantation of a port system for chemotherapy to avoid damage to the peripheral veins;
the use of photodynamic therapy in “non-melanoma” skin cancer (the topical photosensitiser Metvix® cream and the unique Aktilite® photodynamic lamp);
continuous monitoring of the tumour's response to the drugs, allowing oncologists to change the regimen in good time and select more effective agents, which ensures a high survival rate for cancer patients even at an advanced stage;
supportive therapy to minimise the side effects of chemotherapy;
treatment with genuine, latest-generation cytostatic drugs;
an individually tailored radiotherapy plan.
University Hospital Aachen (Uniklinik RWTH Aachen)
University Hospital Halle
University Hospital Cologne
University Hospital Münster
University Hospital Bonn (Universitätsklinikum Bonn)
University Hospital Düsseldorf
University Hospital, Kiel
For a consultation or to order medicines, message our operator.
If the messenger did not open, add us via the phone number:
+4915208811019