Laugier–Hunziker syndrome: a report of three cases and literature review View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2012-12

AUTHORS

Wen-Mei Wang, Xiang Wang, Ning Duan, Hong-Liu Jiang, Xiao-Feng Huang

ABSTRACT

Laugier-Hunziker syndrome (LHS) is an acquired pigmentary condition affecting lips, oral mucosa and acral area, frequently associated with longitudinal melanonychia. There is neither malignant predisposition nor underlying systemic abnormality associated with LHS. Herein, we present three uncommon cases of LHS with possibly new feature of nail pigmentation, which were diagnosed during the past 2 years. We also review the clinical and histological findings, differential diagnosis, and treatment of the syndrome in published literature. More... »

PAGES

ijos201260

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ijos.2012.60

DOI

http://dx.doi.org/10.1038/ijos.2012.60

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1028158058

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/23174847


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