Laugier-Hunziker syndrome - Case report

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 hyperpi...

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Main Authors: Jovan Lalosevic, Dubravka Zivanovic, Dusan Skiljevic, Ljiljana Medenica
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2015-06-01
Series:Anais Brasileiros de Dermatologia
Subjects:
Online Access:http://www.scielo.br/pdf/abd/v90n3s1/0365-0596-abd-90-03-s1-0223.pdf
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author Jovan Lalosevic
Dubravka Zivanovic
Dusan Skiljevic
Ljiljana Medenica
author_facet Jovan Lalosevic
Dubravka Zivanovic
Dusan Skiljevic
Ljiljana Medenica
author_sort Jovan Lalosevic
collection DOAJ
description 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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spelling doaj.art-02842ac35f3d435191d1685041a9ae6d2022-12-21T19:23:31ZengSociedade Brasileira de DermatologiaAnais Brasileiros de Dermatologia0365-05962015-06-01903 suppl 122322510.1590/abd1806-4841.20153840Laugier-Hunziker syndrome - Case reportJovan LalosevicDubravka ZivanovicDusan SkiljevicLjiljana MedenicaAbstractLaugier-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.http://www.scielo.br/pdf/abd/v90n3s1/0365-0596-abd-90-03-s1-0223.pdfHyperpigmentationMouth mucosaNails
spellingShingle Jovan Lalosevic
Dubravka Zivanovic
Dusan Skiljevic
Ljiljana Medenica
Laugier-Hunziker syndrome - Case report
Anais Brasileiros de Dermatologia
Hyperpigmentation
Mouth mucosa
Nails
title Laugier-Hunziker syndrome - Case report
title_full Laugier-Hunziker syndrome - Case report
title_fullStr Laugier-Hunziker syndrome - Case report
title_full_unstemmed Laugier-Hunziker syndrome - Case report
title_short Laugier-Hunziker syndrome - Case report
title_sort laugier hunziker syndrome case report
topic Hyperpigmentation
Mouth mucosa
Nails
url http://www.scielo.br/pdf/abd/v90n3s1/0365-0596-abd-90-03-s1-0223.pdf
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AT ljiljanamedenica laugierhunzikersyndromecasereport