Laugier-Hunziker-Syndrom: Eine seltene Differenzialdiagnose der mukokutanen Hyperpigmentierung

Laugier–Hunziker syndrome (LHS) is characterized by lentiginous hyperpigmentation of the oral mucosa and lips. In addition, longitudinal melanonychia and palmoplantar hyperpigmented lesions may occur. LHS is a clinical diagnosis of exclusion. Herein, we report the case of a 66-year-old woman with LH...

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Detalles Bibliográficos
Autores principales: Korsing, Sören, Boede, Marcel, Ebrahimsade, Schokufe, Meier, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2021
Materias:
Kasuistiken
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964554/
https://www.ncbi.nlm.nih.gov/pubmed/34170334
http://dx.doi.org/10.1007/s00105-021-04845-x
Descripción
Sumario:Laugier–Hunziker syndrome (LHS) is characterized by lentiginous hyperpigmentation of the oral mucosa and lips. In addition, longitudinal melanonychia and palmoplantar hyperpigmented lesions may occur. LHS is a clinical diagnosis of exclusion. Herein, we report the case of a 66-year-old woman with LHS. The clinical and histopathologic features of LHS are presented and important differential diagnoses are discussed.

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