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Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment

The present report describes a case of Laugier-Hunziker syndrome (LHS), a rare benign condition. A patient with LHS develops acquired melanotic pigmentation of the lips and buccal mucosa, often with pigmentation of the nails occurring. No systemic symptoms are associated with this syndrome. Normally...

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Autores principales: Ergun, Sertan, Saruhanoğlu, Alp, Migliari, Dante-Antonio, Maden, Ilay, Tanyeri, Hakkı
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866833/
https://www.ncbi.nlm.nih.gov/pubmed/24367727
http://dx.doi.org/10.1155/2013/561040
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author Ergun, Sertan
Saruhanoğlu, Alp
Migliari, Dante-Antonio
Maden, Ilay
Tanyeri, Hakkı
author_facet Ergun, Sertan
Saruhanoğlu, Alp
Migliari, Dante-Antonio
Maden, Ilay
Tanyeri, Hakkı
author_sort Ergun, Sertan
collection PubMed
description The present report describes a case of Laugier-Hunziker syndrome (LHS), a rare benign condition. A patient with LHS develops acquired melanotic pigmentation of the lips and buccal mucosa, often with pigmentation of the nails occurring. No systemic symptoms are associated with this syndrome. Normally, no treatment is required for this condition, unless for aesthetic reason, mainly due to pigmentation on the lip mucosa. We present a case of LHS, 37-year-old female, whose pigmentations on her lip and in the oral cavity were treated with an Er:YAG laser. At the postoperative 12th month followup, the lesions recurred. The effects of any surgical attempt to treat pigmentations associated with LHS were discussed.
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spelling pubmed-38668332013-12-23 Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment Ergun, Sertan Saruhanoğlu, Alp Migliari, Dante-Antonio Maden, Ilay Tanyeri, Hakkı Case Rep Dent Case Report The present report describes a case of Laugier-Hunziker syndrome (LHS), a rare benign condition. A patient with LHS develops acquired melanotic pigmentation of the lips and buccal mucosa, often with pigmentation of the nails occurring. No systemic symptoms are associated with this syndrome. Normally, no treatment is required for this condition, unless for aesthetic reason, mainly due to pigmentation on the lip mucosa. We present a case of LHS, 37-year-old female, whose pigmentations on her lip and in the oral cavity were treated with an Er:YAG laser. At the postoperative 12th month followup, the lesions recurred. The effects of any surgical attempt to treat pigmentations associated with LHS were discussed. Hindawi Publishing Corporation 2013 2013-12-03 /pmc/articles/PMC3866833/ /pubmed/24367727 http://dx.doi.org/10.1155/2013/561040 Text en Copyright © 2013 Sertan Ergun et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ergun, Sertan
Saruhanoğlu, Alp
Migliari, Dante-Antonio
Maden, Ilay
Tanyeri, Hakkı
Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment
title Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment
title_full Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment
title_fullStr Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment
title_full_unstemmed Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment
title_short Refractory Pigmentation Associated with Laugier-Hunziker Syndrome following Er:YAG Laser Treatment
title_sort refractory pigmentation associated with laugier-hunziker syndrome following er:yag laser treatment
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866833/
https://www.ncbi.nlm.nih.gov/pubmed/24367727
http://dx.doi.org/10.1155/2013/561040
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