Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation

Verena Toedtling; Fiona Carol Crawford

doi:10.1002/ccr3.3522

Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation

Verena Toedtling, Fiona Carol Crawford

Research output: Contribution to journal › Article › peer-review

Abstract

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.

Original language	English
Pages (from-to)	309-313
Journal	Clinical case reports
Volume	9
Issue number	1
Early online date	16 Nov 2020
DOIs	https://doi.org/10.1002/ccr3.3522 https://doi.org/10.1002/ccr3.v9.1
Publication status	Published - 18 Jan 2021

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10.1002/ccr3.v9.1

https://onlinelibrary.wiley.com/doi/10.1002/ccr3.3522

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title = "Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation",

abstract = "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.",

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AB - 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.

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Clinical and histopathological differential diagnosis of Laugier‐Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation

Abstract

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