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Concierge dermatology · London

Mole mapping, total-body photography plus digital dermoscopy for high-risk mole surveillance.

Mole mapping combines total-body photography (typically FotoFinder / MoleMax) with digital dermoscopy of high-risk lesions. Serial imaging over time detects new or changing moles — the modern standard for people at high melanoma risk.

See key facts
A consultant dermatologist performing digital dermoscopy during a mole-mapping session in a private London clinic

Why patients choose us

  • 01

    The right hands

    We route you to a consultant dermatologist — with mole mapping expertise, who images you and who reports it decides the answer.

  • 02

    Serial imaging that catches change

    Total-body photography plus digital dermoscopy — the modern standard for high-risk melanoma surveillance.

  • 03

    Independent, and free

    We are paid by no clinic, so the recommendation is impartial and costs you nothing.

Key facts

Mole mapping at a glance.

The essentials — what mole mapping is, which systems are used, and who benefits.

  • Definition

    Total-body photography plus digital dermoscopy of high-risk lesions.

  • Systems used

    FotoFinder, MoleMax or VECTRA total-body imaging platforms.

  • Why serial imaging

    Detects new lesions and change in existing moles — the pattern melanoma follows.

  • Who it is for

    High melanoma risk — family history, dysplastic-naevus syndrome, prior melanoma.

  • Interval

    Annual, or 6-monthly for the highest-risk patients.

  • Reporting

    Consultant dermatologist with dermoscopy expertise.

The problem

Early melanoma is a change story, not a single-image story.

A single skin check catches obvious lesions. Serial imaging catches new and changing moles — the pattern early melanoma follows. We route you to a consultant dermatologist with dermoscopy expertise, not a generalist.

  • Family history of melanoma?

    We build the baseline image set and set the surveillance interval to your risk.

  • Dysplastic-naevus syndrome?

    AI-assisted change detection over years is the standard of care.

  • Prior melanoma?

    Serial imaging picks up second primary melanomas — a real, avoidable risk.

Diagnosis steps

From consultation to surveillance plan — what happens, in order.

One consultant from first message to report — usually within a week.

  1. 01

    Before

    Consultation and consent

    A short, confidential form. Personal and family melanoma history, prior lesions, skin type, sun-exposure history.

  2. 02

    Before

    We come back with a recommendation

    Within one working day: whether mole mapping is the right test, which clinic, indicative price. If a single-lesion mole check is a better first step, we say so.

  3. 03

    Before

    We arrange the appointment

    Often same or next week, including evenings and Saturdays. Insurer pre-authorisation handled.

  4. 04

    On the day

    Undress to underwear

    You undress to underwear in a private, chaperoned room — that is the whole preparation.

  5. 05

    On the day

    Total-body photography and digital dermoscopy

    30–45 minutes. Total-body photography (FotoFinder, MoleMax or VECTRA) followed by digital dermoscopy of high-risk moles. AI-assisted change detection compares against prior images.

  6. 06

    On the day

    Straight home

    No recovery time. Drive, eat and work as normal.

  7. 07

    After

    Consultant report and surveillance plan

    A written consultant dermatologist report usually within a week, with a structured surveillance interval and onward pathway if any lesion needs excision.

Typical end-to-end: 1–2 weeks. Urgent cases: same week.

What it shows

When mole mapping is the right test.

Mole mapping answers a specific question — is anything on your skin new or changing since baseline. These are the situations we see most.

  • New lesion detection

    Serial imaging flags moles that were not there at baseline.

  • Change in existing lesion

    Shape, colour or size change picked up against the prior image set.

  • Atypical (dysplastic) naevus

    Characterises borderline lesions that need closer monitoring.

  • Early melanoma

    The earliest melanomas are found by change detection, not by a single look.

  • Baseline for future comparison

    One high-quality image set becomes the reference for every future visit.

  • High-risk-group serial monitoring

    Structured surveillance for family-history and dysplastic-naevus patients.

  • Post-melanoma follow-up

    Detects second primary melanomas — a real risk after a first diagnosis.

  • Red flag: EFG lesion — evolving, firm, growing — urgent excision

    An EFG lesion is not for surveillance. Same-week excision is the answer.

Treatment options

What follows a mole-mapping visit.

Every finding maps to a concrete next step — reassurance, excision, adjusted interval or onward MDT.

  • Reassurance for stable pattern

    When the image set is unchanged, the answer is a structured surveillance interval — not intervention.

  • Excision of new or changing lesion

    Any new or changed lesion that meets dermoscopic criteria is excised for histology.

  • Photographic surveillance interval

    Annual for most, 6-monthly for the highest-risk patients — the interval is set to your risk.

  • Sun-protection advice

    Personalised UV-protection advice for your skin type and exposure pattern.

  • Vitamin D discussion

    Practical guidance on maintaining vitamin D while minimising melanoma risk.

  • Family cascade screening

    For dysplastic-naevus syndrome or a strong family history, first-degree relatives are offered screening.

  • Melanoma MDT for confirmed cancer

    If histology confirms melanoma, referral into a specialist skin-cancer MDT with staging and wide local excision.

  • Structured dermatology follow-up

    A named consultant, a named interval, and a written plan — not ad-hoc appointments.

Our vetted London network

A small panel of clinics, we picked them.

Partners across central, north, west and south London. Not listed publicly — introductions are made privately, once we understand your case.

Selection criteria

How we choose every clinic in our network.

A modern London dermatology room with a current-generation total-body imaging platform
Consultant dermatologists
  • Consultant dermatologists with total-body photography and dermoscopy expertise

  • FotoFinder, MoleMax or VECTRA total-body imaging platforms

  • AI-assisted change detection against prior image sets

  • Onward skin-cancer MDT pathway if excision confirms melanoma

Red flags and safety

Non-invasive — but the red flags matter.

Mole mapping is safe and painless. The practical points are which lesions bypass surveillance and go straight to excision, and where photography does not go.

  • Non-invasive, radiation-free

    Photography and dermoscopy — no needles, no radiation, no dye.

  • Chaperoned, private room

    Every session is chaperoned. You undress only to underwear.

  • A new pigmented lesion in an adult is a red flag

    Any new mole after age 40 deserves a dermatology opinion, not a photograph alone.

  • Rapidly changing mole — do not wait

    A visibly changing lesion needs a same-week dermatology appointment, not the next surveillance slot.

  • EFG lesion — evolving, firm, growing

    EFG lesions bypass surveillance. Direct-to-excision is the answer.

  • Nail-bed and mucosal melanoma

    Melanoma can arise under a nail or on a mucous membrane. These are checked at every visit.

  • Amelanotic melanoma

    A minority of melanomas have little or no pigment — dermoscopy remains essential.

  • Immunosuppressed and post-transplant

    Skin-cancer risk is materially raised. Surveillance intervals are shortened accordingly.

  • Photographs do not replace an examination

    Mole mapping supports — it does not replace — a hands-on consultant skin examination.

Reading your report

A mole-mapping report can look intimidating. It isn’t.

Whatever the finding, the report keeps to the same four parts.

A consultant dermatologist reviewing digital dermoscopy images on a clinical workstation at a UK private clinic

A quiet reminder

The report is written for your doctor, not for you — and that’s normal.

If you would like us to talk you through it before your follow-up, just ask.

  1. 01 Header

    Indication and risk factors

    Your details, personal and family melanoma history, skin type, and the reason for surveillance.

  2. 02 Technique

    Imaging platform and dermoscopy

    Which total-body system (FotoFinder / MoleMax / VECTRA), which lesions had digital dermoscopy, and how AI-assisted change detection was applied.

  3. 03 Findings

    New, changed and stable lesions

    Lesion-by-lesion description: new moles, changed moles, atypical dermoscopic features and stable comparators.

  4. 04 Impression

    The conclusion: read this first

    Stable pattern, surveillance interval, and any lesion recommended for excision — read this first.

Recognised by major UK insurers

BupaAXA HealthVitalityAvivaWPACignaHealixBupaAXA HealthVitalityAvivaWPACignaHealixBupaAXA HealthVitalityAvivaWPACignaHealix

Cover depends on your policy and clinic; we confirm with your insurer before booking.

Frequently asked

Everything we get asked about mole mapping.

Quick answers on who benefits, how it differs from a mole check, how often to repeat, referrals, pregnancy and safety.

  • What does mole mapping show?

    Mole mapping combines total-body photography with digital dermoscopy of high-risk lesions. Serial images over time detect new moles and change in existing ones — the pattern early melanoma follows.

  • What is the difference between a mole check and mole mapping?

    A mole check is a consultant examination of one or a few lesions of concern. Mole mapping is total-body photography plus digital dermoscopy, designed for serial surveillance of high-risk patients over years.

  • Who should have mole mapping?

    Anyone at high melanoma risk — a personal or strong family history of melanoma, dysplastic-naevus syndrome, many atypical moles, prior melanoma, or long-term immunosuppression. We will say up front if a single mole check is a better first step.

  • How often should mole mapping be repeated?

    Annual for most high-risk patients; 6-monthly for the highest-risk groups (post-melanoma, dysplastic-naevus syndrome, transplant patients). The interval is a consultant decision, not a fixed rule.

  • Do I need a referral?

    Most clinics accept self-referral for mole mapping. We can arrange a fast-track private GP if a formal referral is needed for insurance or onward pathway.

  • Is mole mapping safe in pregnancy?

    Entirely safe — photography and dermoscopy use light, not radiation, and are appropriate at any stage of pregnancy.

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In practice, in London

Why private mole mapping moves differently in London

With mole mapping, the London question is usually about report turnaround and the radiologist reading it — not whether the scan is available. On the NHS, mole mapping typically sits behind a triage step and a wait that can stretch from a few weeks into months. In London’s private sector, the same appointment often lands within days. That speed matters when symptoms are disrupting work, sleep, or a plan you’d already committed to — and it’s the single most common reason people call us in the first place.

The mechanics are straightforward: a consultant appointment, any tests done at a nearby CQC-registered site, and a written report back within a few days. London’s density of private diagnostics — Marylebone, the City, Chelsea, Canary Wharf — means most patients can find something that fits around work without a cross-town trek. For mole mapping specifically, the difference between a routine report and a sub-speciality read is where private care earns its keep.

The value of going through a concierge for mole mapping isn’t access — anyone with an insurer or a credit card can get a private appointment in London. The value is knowing which consultant reads this particular presentation best, which unit turns reports around fastest, and which pathway won’t hit a dead end if the findings point somewhere unexpected.

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