Anais Brasileiros de Dermatologia (Jun 2015)

Laugier-Hunziker syndrome - Case report

  • Jovan Lalosevic,
  • Dubravka Zivanovic,
  • Dusan Skiljevic,
  • Ljiljana Medenica

DOI
https://doi.org/10.1590/abd1806-4841.20153840
Journal volume & issue
Vol. 90, no. 3 suppl 1
pp. 223 – 225

Abstract

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AbstractLaugier-Hunziker syndrome is a rare, acquired disorder characterized by lenticular hyperpigmentation of the oral mucosa and longitudinal melanonychia. We present the case of a 63-year-old female with progressive, asymptomatic hyperpigmentation of buccal mucosa and a 7-year history of hyperpigmentation in several fingernails. Laugier-Hunziker syndrome was diagnosed based on the clinical features presented, dermoscopic findings and exclusion of underlying systemic diseases. Laugier-Hunziker syndrome is regarded as a diagnosis of exclusion. By identifying Laugier-Hunziker syndrome, other, more severe syndromes associated with hyperpigmentations can be excluded, namely Addison’s disease and Peutz-Jeghers syndrome.

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