Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteria

ABSTRACT Laugier-Hunziker syndrome (LHS) is a rare mucocutaneous disorder, of unknown etiology, characterized by multiple hyperpigmented macules, dispersed mostly on the oral mucosa, occasionally associated with longitudinal ridging of the nails. The diagnosis requires exclusion of other conditions,...

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Main Authors: Luiz Arthur B. Silva, Rodrigo P. Mafra, Patrícia T. Oliveira, Ana Miryam C. Medeiros, Leão P. Pinto, Éricka Janine D. Silveira
Format: Article
Language:English
Published: Sociedade Brasileira de Patologia Clínica 2018-02-01
Series:Jornal Brasileiro de Patologia e Medicina Laboratorial
Subjects:
Online Access:http://www.scielo.br/pdf/jbpml/v54n1/1676-2444-jbpml-54-01-0052.pdf
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author Luiz Arthur B. Silva
Rodrigo P. Mafra
Patrícia T. Oliveira
Ana Miryam C. Medeiros
Leão P. Pinto
Éricka Janine D. Silveira
author_facet Luiz Arthur B. Silva
Rodrigo P. Mafra
Patrícia T. Oliveira
Ana Miryam C. Medeiros
Leão P. Pinto
Éricka Janine D. Silveira
author_sort Luiz Arthur B. Silva
collection DOAJ
description ABSTRACT Laugier-Hunziker syndrome (LHS) is a rare mucocutaneous disorder, of unknown etiology, characterized by multiple hyperpigmented macules, dispersed mostly on the oral mucosa, occasionally associated with longitudinal ridging of the nails. The diagnosis requires exclusion of other conditions, such as Addison's disease and Peutz-Jeghers syndrome. We report a case of a 34-year-old male patient, presenting with hyperpigmented macules on the lips, buccal mucosa and palate, as well as mild dark striations on toenails. After careful clinical and laboratorial investigations, the diagnosis of LHS was established. Given the lack of aesthetic complaints and symptoms, no treatment was necessary.
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spelling doaj.art-d4e55d96f8c244f8b0ddede6543260712022-12-22T04:09:20ZengSociedade Brasileira de Patologia ClínicaJornal Brasileiro de Patologia e Medicina Laboratorial1678-47742018-02-01541525610.5935/1676-2444.20180011Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteriaLuiz Arthur B. SilvaRodrigo P. MafraPatrícia T. OliveiraAna Miryam C. MedeirosLeão P. PintoÉricka Janine D. SilveiraABSTRACT Laugier-Hunziker syndrome (LHS) is a rare mucocutaneous disorder, of unknown etiology, characterized by multiple hyperpigmented macules, dispersed mostly on the oral mucosa, occasionally associated with longitudinal ridging of the nails. The diagnosis requires exclusion of other conditions, such as Addison's disease and Peutz-Jeghers syndrome. We report a case of a 34-year-old male patient, presenting with hyperpigmented macules on the lips, buccal mucosa and palate, as well as mild dark striations on toenails. After careful clinical and laboratorial investigations, the diagnosis of LHS was established. Given the lack of aesthetic complaints and symptoms, no treatment was necessary.http://www.scielo.br/pdf/jbpml/v54n1/1676-2444-jbpml-54-01-0052.pdfhyperpigmentationmouth mucosaskin abnormalities
spellingShingle Luiz Arthur B. Silva
Rodrigo P. Mafra
Patrícia T. Oliveira
Ana Miryam C. Medeiros
Leão P. Pinto
Éricka Janine D. Silveira
Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteria
Jornal Brasileiro de Patologia e Medicina Laboratorial
hyperpigmentation
mouth mucosa
skin abnormalities
title Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteria
title_full Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteria
title_fullStr Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteria
title_full_unstemmed Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteria
title_short Oral pigmentations in Laugier-Hunziker syndrome: a case report and review of diagnostic criteria
title_sort oral pigmentations in laugier hunziker syndrome a case report and review of diagnostic criteria
topic hyperpigmentation
mouth mucosa
skin abnormalities
url http://www.scielo.br/pdf/jbpml/v54n1/1676-2444-jbpml-54-01-0052.pdf
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