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Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation
Laugier‐Hunziker syndrome is a rare and benign disorder characterized by hyperpigmentation of the lips and buccal mucosae with associated longitudinal melanonychia of nails. Clinical correlation is needed to rule out other pigmentary disorders.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813034/ https://www.ncbi.nlm.nih.gov/pubmed/33489178 http://dx.doi.org/10.1002/ccr3.3522 |
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author | Toedtling, Verena Crawford, Fiona Carol |
author_facet | Toedtling, Verena Crawford, Fiona Carol |
author_sort | Toedtling, Verena |
collection | PubMed |
description | Laugier‐Hunziker syndrome is a rare and benign disorder characterized by hyperpigmentation of the lips and buccal mucosae with associated longitudinal melanonychia of nails. Clinical correlation is needed to rule out other pigmentary disorders. |
format | Online Article Text |
id | pubmed-7813034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78130342021-01-22 Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation Toedtling, Verena Crawford, Fiona Carol Clin Case Rep Case Reports Laugier‐Hunziker syndrome is a rare and benign disorder characterized by hyperpigmentation of the lips and buccal mucosae with associated longitudinal melanonychia of nails. Clinical correlation is needed to rule out other pigmentary disorders. John Wiley and Sons Inc. 2020-11-16 /pmc/articles/PMC7813034/ /pubmed/33489178 http://dx.doi.org/10.1002/ccr3.3522 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Toedtling, Verena Crawford, Fiona Carol Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation |
title | Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation |
title_full | Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation |
title_fullStr | Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation |
title_full_unstemmed | Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation |
title_short | Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation |
title_sort | clinical and histopathological differential diagnosis of laugier‐hunziker syndrome: an extremely rare case with unusual extensive oral hyperpigmentation |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813034/ https://www.ncbi.nlm.nih.gov/pubmed/33489178 http://dx.doi.org/10.1002/ccr3.3522 |
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