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This is a PatientPlus article. PatientPlus articles are written for doctors and so the language can be technical, however some people find that they add depth to the patient information leaflets. You may find the abbreviations record helpful.

Synonyms: Tièche-Jadassohn naevus,1 Jadassohn-Tièche naevus,1 common blue naevus, cellular blue naevus, chromatophoroma, melanofibroma.

A blue naevus is a small blue- or grey-coloured lesion of the skin, with an appearance similar to a mole. They derive their blue colour from their pigmentation with melanin and relatively deep position within the epidermis. One theory of their origin is that they represent embryonic neural crest cells that have failed to migrate into the epidermis in the usual fashion.2 There are two forms:

  • Common blue naevus:
    • Commonest form, 2–7 mm in diameter.
    • Slightly raised and smooth lesion with macular, papular or plaque-like appearance.
    • Grey-blue to bluish-black in colour.
    • Does not have any malignant potential.
    • Usually a solitary lesion with a predilection for head (especially scalp), neck, sacral area and dorsum of the hands/feet.
  • Cellular blue naevus:
    • Much rarer than the common form.
    • Larger lesion, often 1–3 cm in diameter.
    • Raised lesions with a smooth surface.
    • Same colour as common form.
    • Often solitary and found on buttocks, sacral region and back of hands/feet.
    • May represent a subgroup of atypical melanoma, but this is uncertain, although the potential of the cellular form to undergo malignant transformation has been observed rarely.3
Epidemiology
  • They are present from a young age, but relatively unusual at birth (estimated prevalence ~1 in 1,000).2
  • Commonest in Asian populations with a prevalence of 3–5% among adults. Prevalence in white populations is roughly 1–2%.
  • Around twice as common in women compared to men.2
Visual appearance

Classical appearance of a common blue naevus
BLUE NAEVUS -CLOSE UP (DIS16.jpg)

Presentation
  • Usually arise during the second decade and do not change in shape or size thereafter.
  • They can rarely be present from birth.
  • If the cellular form of the lesion undergoes malignant transformation this usually manifests as a precipitate increase in size or, more rarely, ulceration.2
  • Can be found as pigmented lesions at unusual sites, e.g. female genito-urinary tract,4 oral mucosa,5 beneath nails, spermatic cord, bronchus, lymph nodes and prostate.
Differential diagnosis6
Associated diseases
  • Carney's syndrome/complex is a rare association of blue naevi with further abnormalities of the skin and other organs, inherited in an autosomal dominant fashion.
  • It causes cardiac, endocrine, cutaneous and neural myxomatous tumours, plus a variety of pigmented lesions of the skin and mucosae.7
Investigations
  • None usually required.
  • If the nature of a lesion is uncertain then dermoscopy may be performed by a dermatologist to distinguish it from melanomatous lesions.
Management
  • Typical lesions that have the appropriate history, that have not changed in size or shape and where there are no other features that would suggest an alternative diagnosis, or the presence of melanoma, can be left alone, and the patient reassured.
  • However, as for any pigmented lesion, where there is doubt as to the diagnosis it is safest to perform excision biopsy or refer for dermatological advice.
  • Where the history is atypical, or the lesion has changed, refer for advice or perform excision biopsy.
  • There are occasional reports of recurrence of the lesion in a satellite form after excision; such lesions must be examined by further excision biopsy, preferably with dermatological opinion, to exclude malignant transformation.2
Complications
  • Common blue naevi do not have any complications, are benign, and persist unchanged throughout life.
  • Cellular blue naevi are also usually benign but may rarely undergo malignant transformation.
  • Cellular naevi are larger and so more likely to present and undergo excision biopsy.
Prognosis
  • The prognosis for both types of lesion is excellent.
  • In the rare cases where cellular naevi become malignant then prognosis is improved by earlier diagnosis, as for melanoma.


Document references
  1. Whonamedit.com, Tieche-Jadassohn naevus.; Historical and biographical information on the lesion's eponymous discoverers.
  2. Roth R, Acker S; Blue Nevi; eMedicine, March 2009.
  3. Aloi F, Pich A, Pippione M; Malignant cellular blue nevus: a clinicopathological study of 6 cases. Dermatology. 1996;192(1):36-40. [abstract]
  4. Rochanawutanon M; Blue nevus of the uterine cervix. J Med Assoc Thai. 1992 Jan;75 Suppl 1:94-7. [abstract]
  5. Buchner A, Hansen LS; Pigmented nevi of the oral mucosa: a clinicopathologic study of 32 new cases and review of 75 cases from the literature. Part II. Analysis of 107 cases. Oral Surg Oral Med Oral Pathol. 1980;49(1):55-62. [abstract]
  6. Univ. Iowa; Dept. of Dermatology - College of Medicine, Dermatology Differential Diagnosis by Morphology, Differential by colour (blue).
  7. OMIM: On-line Mendelian Inheritance in Man, Carney complex 1.

Internet and further reading Acknowledgements EMIS is grateful to Dr Colin Tidy for writing this article and to Dr Sean Kavanagh for earlier versions. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
Document ID: 4063
Document Version: 22
Document Reference: bgp25996
Last Updated: 27 Jul 2009
Planned Review: 27 Jul 2011

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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