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Living with Large congenital melanocytic nevus

A condition present from birth with a very large, dark, noncancerous skin patch made of pigment cells.

Understanding Large congenital melanocytic nevus

Large (giant) congenital melanocytic nevus is a skin condition with an unusually dark, noncancerous patch of pigment-producing cells present from birth.

The patch may be small in infants but grows with the body and will eventually be at least 40 cm (about 16 inches) across. It is often on the trunk or limbs. Color ranges from tan to black, and the surface can be flat, rough, raised, or bumpy. The skin may be dry, itchy, thin, or hairy. Some people have additional smaller nevi. Some have neurocutaneous melanosis, with pigment cells in the tissue covering the brain and spinal cord. The look of the nevus may cause worry or stress.

Signs & symptoms

Symptoms vary from person to person. GARD lists these among the most common:

  • Large, dark skin patch present from birth
  • Dry, itchy skin in the patch
  • Extra hair growth in the patch
  • Thin skin in the patch
  • Additional smaller moles
  • Poor wound healing

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Specialists who may be involved include cancer specialists, genetic specialists and skin, hair, and nail specialists.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

  4. Connect with expert centers

    Melanoma Research Foundation may keep lists of experts for this condition.

Care & treatment

Care team
Cancer specialists (oncologists); Genetic specialists (geneticists); Skin, hair, and nail specialists (dermatologists)
Expert care
Expert lists: Melanoma Research Foundation
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Melanoma Research Foundation and other patient organizations
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
Is my child at risk for neurocutaneous melanosis, and should an MRI be done?
How often should the nevus be checked by a skin specialist?
What emotional support is available for my child?

Quick facts

Symptoms usually startNewborn and as an Infant

GARD says changes in genes (also called variants) cause this condition. It does not name specific genes or describe inheritance.

GeneticSkin

Also known as: bathing trunk nevus; cmns; congenital giant melanocytic nevus; congenital giant pigmented nevus; congenital melanocytic nevi; congenital melanocytic nevus

Patient organizations

Source: NIH GARD · Large congenital melanocytic nevusGARD ID 2469 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Large congenital melanocytic nevus.

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