Congenital Dermal Melanocytosis

(FORMERLY KNOWN AS MONGOLIAN BLUE SPOT)

What are the aims of this leaflet?

This leaflet has been written to help you understand more about congenital dermal melanocytosis. It tells you what it is, what causes it, what can be done about it, and where you can find out more about it.

What is congenital dermal melanocytosis?

Congenital dermal melanocytosis is a common, harmless, pigmented birthmark. It is sometimes also called lumbrosacral dermal melanocytosis, and is sometimes still referred to by its old name of a Mongolian Blue Spot. It is
usually seen at birth or shortly afterwards. It typically disappears before the age of 6.

What causes congenital dermal melanocytosis?

During the baby’s development in the womb, cells called melanocytes move from deeper in the skin (a layer called the dermis) to the top layer of the skin (the epidermis) by the 20th week of pregnancy. Melanocytes produce
melanin, which is the pigment responsible for skin, hair and eye colour. In congenital dermal melanocytosis, these cells remain in the dermis at birth and continue to produce melanin. The reason for this is unknown. Melanin in the
dermis appears blue-grey through the skin, which is why congenital dermal melanocytosis looks like a blue-grey patch on the skin.

Is congenital dermal melanocytosis hereditary?

There may be an underlying inherited cause for this condition, as they are very common in children of Asian, African, Middle Eastern, or Mediterranean descent. They are rare in children with fair skin.

What are the symptoms of congenital dermal melanocytosis?

There are no physical symptoms associated with congenital dermal melanocytosis. The affected areas of skin are not itchy or painful.

What does congenital dermal melanocytosis look like?

They are flat, blue-grey, non-raised patches that can appear anywhere on the skin, but most commonly on the lower back and buttocks. They occur rarely on the abdomen and limbs, and very rarely on the face and scalp. It can be
seen as a single patch or multiple patches close together.

Where a very large amount of skin is affected, very rarely this may be associated with inborn errors of metabolism (rare inherited disorders where the body cannot adequately break down food). Your doctor will arrange further
tests if they think this could be a possibility.

How is congenital dermal melanocytosis diagnosed?

Congenital dermal melanocytosis is usually diagnosed by a doctor, based on its characteristic typical appearance at birth or shortly after. No other diagnostic investigations are required.

Due to the colour and location, they can be mistaken for bruises, which can happen with non-accidental injury. Therefore, it is important that your doctor or midwife record the presence of congenital dermal melanocytosis in the
baby and maternal records at initial assessment, to avoid misdiagnosis as bruising at a later date.

How can congenital dermal melanocytosis be treated?

Congenital dermal melanocytosis does not require any treatment as the majority disappear by the age of 6. In rare cases, they can persist into puberty and very rarely indefinitely. If the patches do not fade and are causing distress, then options like skin camouflage can be considered where the skin is visible.

Where can I get more information about congenital dermal melanocytosis?

Web links to detailed leaflets:

https://dermnetnz.org/topics/lumbosacral-dermal-melanocytosis/
http://www.pcds.org.uk/clinical-guidance/mongolian-spot

Links to patient support groups:

Birthmark Support Group
Tel: 07825 855 888
Email: info@birthmarksupportgroup.org.uk
Web: http://www.birthmarksupportgroup.org.uk/

Changing Faces
Tel: 0300 012 0275 (for support and advice)
Tel: 0300 012 0276 (for the Skin Camouflage Service)
Email: skincam@changingfaces.org.uk
Web: www.changingfaces.org.uk

British Association of Skin Camouflage (NHS and private practice)
Tel: 01254 703 107
Email: info@skin-camouflage.net
Web: www.skin-camouflage.net

For details of source materials used please contact the Clinical Standards Unit (clinicalstandards@bad.org.uk).

This leaflet aims to provide accurate information about the subject and is a consensus of the views held by representatives of the British Association of Dermatologists: individual patient circumstances may differ, which might alter both the advice and course of therapy given to you by your doctor.

This leaflet has been assessed for readability by the British Association of Dermatologists’ Patient Information Lay Review Panel

BRITISH ASSOCIATION OF DERMATOLOGISTS
PATIENT INFORMATION LEAFLET
PRODUCED JANUARY 2021
REVIEW DATE JANAURY 2024

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