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Halo Naevus

Synonyms: Sutton's naevus, leukoderma acquisita centrifugum.

Description

This is a benign skin lesion that is a result of a common melanocytic naevus undergoing an inflammatory process, such that a zone of depigmentation surrounds the mole. There is an infiltration of T-lymphocytes and macrophages and possibly some antibody-mediated autoimmunity. The aetiology and pathophysiology of the immune reaction to the presence of an aggregate of melanocytes is poorly understood.

The lesion can cause significant anxiety in its sufferers due to its characteristic and striking appearance. The central naevus may undergo involution leaving a grey or white halo that can resemble melanoma that has undergone regression, leaving the clinician with a diagnostic dilemma, on ocassions.1

Visual appearance

Typical early appearance of a halo naevus

HALO NAEVUS -CLOSE UP (DIS44.jpg)

Epidemiology

They are common lesions and estimated to have a prevalence in the general population of about 1% in the US.1 Turner's syndrome patients have a higher prevalence of halo naevi than the general population.2 Some families may have a tendency to the lesions.1

Presentation
  • Halo naevi most commonly affect younger people and the average age of onset is about 15 years.1
  • They are usually asymptomatic lesions, apart from the cosmetic disturbance that they cause.
  • The central naevus may involute and then subsequently repigment, over a period of years.
  • There may be occasional inflammatory crusting within the depigmented zone.
  • The lesion may be solitary but may occur multiply on occasion.
  • They are most commonly found on the trunk but can occur at any site.
  • They usually consist of a central uniformly pigmented naevus, usually round or oval in shape, with a surrounding area of depigmentation of uniform width from the naevus's edge.
  • Where the naevus has undergone involution there may just be an isolated white circular/oval macule.
Differential Diagnosis

The lesion has a characteristic appearance that usually means it is not confused with other diagnoses. The following problems can present with a similar appearance and should be considered as the cause of a depigmented lesion, but should usually be able to be discriminated on the grounds of their history or appearance:

Investigations
  • None are required if the lesion has a typical history and appearance.
  • A Wood's UV lamp may be used to distinguish diagnoses such as tinea/pityriasis versicolor.
  • Dermoscopy may be used to demonstrate characteristic patterns of pigmentation associated with benign melanocytic naevi.3
  • If there is any uncertainty as to the nature of the lesion, consider dermatological referral or excision biopsy to exclude melanoma.
  • Features that would prompt the need for excision biopsy include:
    • Irregularity of the margin of the pigmented or depigmented zones
    • Non-uniformity of overall shape
    • Papular component that is not centrally located
    • Rapid growth of the lesion
    • Rapid increase in pigmentation of the pigmented zone
    • Irritation, bleeding or ulceration of the lesion.
Associated Diseases

Turner's syndrome.2

Management

Halo naevi are benign lesions that require no active management other than reassurance of the patient.

Complications

There are no complications as such, unless the lesion is misdiagnosed, or there are problems associated with excision biopsy.

Prognosis

Excellent.


Document References
  1. Zabawski E, Cockerell C, eMedicine, Halo Nevus, 2005.
  2. Brazzelli V, Larizza D, Martinetti M, et al; Halo nevus, rather than vitiligo, is a typical dermatologic finding of turner's syndrome: clinical, genetic, and immunogenetic study in 72 patients. J Am Acad Dermatol. 2004 Sep;51(3):354-8. [abstract]
  3. Kolm I, Di Stefani A, Hofmann-Wellenhof R, et al; Dermoscopy patterns of halo nevi. Arch Dermatol. 2006 Dec;142(12):1627-32. [abstract]

Internet and Further Reading
  • NICE, Improving Outcomes for People with Skin Tumours including Melanoma, Guidance, 2006.
Acknowledgements EMIS is grateful to Dr Sean Kavanagh for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2007.
DocID: 4066
Document Version: 20
DocRef: bgp25999
Last Updated: 21 Feb 2007
Review Date: 20 Feb 2009

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