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Malignant melanoma — in Germany commonly called “schwarzer Hautkrebs”, black skin cancer — arises from the pigment cells of the skin, the melanocytes. Some melanomas grow out of an existing mole, most of them on skin that looked unremarkable. It often spreads across the surface first, but it can then grow into the depths and send out secondaries. That is why time is the decisive factor here: spotted early and removed completely, the outlook is usually very good.¹,²
Moles are normal; what is suspicious is not how many you have but change. Melanoma is often lumped together with non-melanoma skin cancer: that form is more common, grows more slowly and only rarely spreads. Melanoma is rarer, but it can metastasise earlier — which is why a new, dark, changing patch means an appointment soon.²,³
The ABCDE rule is the core of early detection. It does not replace a diagnosis, but it answers the question: do I need to take this to a dermatology practice? A patch does not have to meet every criterion — one point that clearly applies is enough.
Once a month, in good light, with a hand mirror and a wall mirror — systematically.
Melanomas are classified by their growth pattern — which matters, because not every type fits the “dark patch” picture.¹,⁴
| Type | Typical appearance | Preferred sites |
|---|---|---|
| Superficial spreading | Flat patch, irregularly coloured | Trunk, back, legs — the most common type |
| Nodular | Raised, fast-growing nodule | Anywhere; grows into the depths early |
| Lentigo maligna | Large, blurred patch developing over years | Face, older age |
| Acral lentiginous | Blurred patch or a streak in a nail | Palms, soles of the feet, nails |
| Amelanotic | Barely pigmented, reddish | Anywhere; often mistaken for a wart |
The report will later state the Breslow tumour thickness in millimetres — how deep the tumour has grown into the skin. It counts as the single most important prognostic factor; the safety margin and the sentinel lymph node procedure are guided by it as well. A stage is a statement of probability for groups, not a prediction for you personally.¹
The most important cause you can influence is UV radiation — though not in the way many people assume: for melanoma, what counts above all is occasional, intense exposure with sunburn, rather than the lifetime total dose.²,³
People with statutory health insurance are generally entitled to a skin cancer screening every two years from the age of 35 — a whole-body examination of the skin including the hairy scalp, with no co-payment. If your risk is increased, closer checks are possible.³
Treatment depends on tumour thickness and stage; the first step, and in early stages usually the only one, is surgery. Everything beyond that is as a rule discussed in a tumour board — and always decided together with you.¹
This is the part that takes the most organising and gets talked about the least: after a melanoma, treatment does not end with the last stitch. The German S3 guideline provides for risk-adapted follow-up over around ten years — close together at the start, at longer intervals afterwards. The reason is twofold: relapses usually occur early, and anyone who has had a melanoma carries an increased risk of a second, independent one.¹
| Period | What usually happens | What you contribute |
|---|---|---|
| First years | Shortest intervals: the whole skin, the scar and the lymph nodes, with ultrasound depending on the stage | Monthly self-check, photos, noting down symptoms |
| Middle phase | Longer intervals, the same scope, less equipment-based diagnostics | Book appointments early — waiting times are often long |
| Up to around year ten | Mainly skin checks, to catch a second tumour early | Keep up sun protection, keep the medication list current |
Ask for the plan in writing and enter the appointments straight away. The most common failure is not a lack of motivation but the appointment that quietly disappears in year three. The follow-up folder should hold the histology report, the operation report, the follow-up plan, photos and an up-to-date medication list.
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This is where melanoma prevention and medication management touch — and it is exactly the point that regularly gets lost in consultations. A number of common medicines increase the skin’s sensitivity to light (photosensitisation): you burn faster than you otherwise would. And sunburn is the risk factor you can actually influence.²,⁵
| Active substance | Typical use | What to watch out for |
|---|---|---|
| Doxycycline | Antibiotic for respiratory and skin infections, acne | Marked photosensitisation is possible. Avoid direct sun, use a high sun protection factor — even on short courses |
| Isotretinoin | Severe acne | The skin becomes thinner and considerably more sensitive to light. Consistent sun protection for the whole of the treatment; on top of that, strict requirements in pregnancy |
| Hydrochlorothiazide | Diuretic for high blood pressure, often in fixed combinations | Increases sensitivity to light. For non-melanoma skin cancer a link with long-term use has been described; for melanoma the evidence is less clear-cut — skin checks make sense |
| Other groups | Certain antibiotics, anti-inflammatory drugs, psychiatric medicines, St John’s wort | The package leaflet lists it under “sensitivity to light”. If in doubt, ask at the pharmacy |
Typically this shows as a sunburn-like skin rash on exposed areas, often with itching and more severe than the time in the sun would lead you to expect. Details in the guide medications and sun.
The immune system clears out degenerate cells continuously. If it is permanently dampened, that works less well — which is why people on long-term immunosuppression develop skin tumours more often. The effect is clearest after organ transplantation; it is better established for non-melanoma skin cancer than for melanoma.²,⁴
These medicines are given for good reasons, and the benefit usually clearly outweighs the risk. The right response is not to stop them but closer skin checks plus UV protection. Say at your appointment that you take them — that often changes the interval between checks.
And a word about the mind: after a melanoma diagnosis, fear of every new patch is normal. What helps is a clear framework — a fixed self-check, fixed follow-up appointments, and deliberately not looking all the time in between. If worry starts to run your day, psycho-oncological support is part of the treatment.
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