Anais Brasileiros de Dermatologia (Jan 2017)

Porokeratotic eccrine and hair follicle nevus: a report of two cases and review of the literature

  • Alfredo Daniel Agulló-Pérez,
  • Miguel Ángel Resano-Abarzuza,
  • Alicia Córdoba-Iturriagagoitia,
  • Juan Ignacio Yanguas-Bayona

DOI
https://doi.org/10.1590/abd1806-4841.20176536
Journal volume & issue
Vol. 92, no. 5 suppl 1
pp. 121 – 125

Abstract

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Abstract: Porokeratotic eccrine and hair follicle nevus is a very rare non-hereditary disorder of keratinization with eccrine and hair follicle involvement with only 9 cases described in the literature. In 2009 the term porokeratotic anexial ostial nevus was proposed to comprehend porokeratotic eccrine and hair follicle nevus and a related and more common process without follicular involvement: porokeratotic eccrine ostial and dermal duct nevus Recent findings suggest that both entities may be produced by a mutation in GJB2 gene, which is associated to KID syndrome. Herein we report 2 cases of porokeratotic eccrine and hair follicle nevus and review the existing cases in the Spanish and English literature.

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