1. Cornbleet T, Bernstein R, Kroll C. Observations on leukoderma acquistum centrifugum. Arch Dermatol. 1960;82:1011-2. 2. Meyerson KB. A peculiar papulosquamous eruption involving pigmented naevi. Arch Dermatol. 1971;103:510-2. 3. Del Río E, Aguilar A, Gallego MA. Targetoid halo nevus. J Am Acad Dermatol. 1993;29:267-8. 4. Fabrizi G, Massi G. Halo naevus with histological changes resembling epi...

Le naevus bleu cellulaire atypique est une entité pathologique rare et sa localisation au niveau du poignet est exceptionnelle. Il est Considéré comme une Variante à des caractéristiques intermédiaires entre le naevus bleu cellulaire typique et le naevus bleu malin, dont l'évolution est incertaine. Le but de notre travail est d'attirer l'attention sur cette variété lésionnelle rare et de discut...

Epidermolysis bullosa naevi are large, eruptive melanocytic naevi which frequently arise in areas of former blisters in patients suffering from inherited epidermolysis bullosa. Morphologically, these naevi are similar to malignant melanoma, although so far no malignant transformation has been observed. To investigate the pathogenesis of these moles we documented their clinical evolution and the...

Epidermal naevi are hamartomas that are characterized by hyperplasia of the epidermis and adnexal structures and may be associated with serious disfiguration. Management of epidermal naevi is challenging. We present here our experience with cryosurgery in the treatment of verrucous epidermal naevi. The aim of this study was to determine the efficacy and safety of cryosurgery for the treatment o...

The occasional occurrence of hypertrophy of a limb associated with cutaneous naevi or haemangiomata, together with congenital or developmental defects of the arteries and veins, has long been recognized. In 1858 Adams described a 'singular case of Hypertrophy of the Right Lower Extremity with Superficial Cutaneous Naevus of the Same Side.' This appears to be the first description of such a cond...

White sponge naevus occurred in association with coloboma of the iris in six members of one family, across three generations. The association of these two dominantly inherited conditions has not to our knowledge previously been described.