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Case Reports
. 2005 Sep-Oct;71(5):354-6.
doi: 10.4103/0378-6323.16790.

Laugier-Hunziker pigmentation

C Ajith  1 , Sanjeev Handa
Affiliations
Case Reports

Laugier-Hunziker pigmentation

C Ajith et al. Indian J Dermatol Venereol Leprol. 2005 Sep-Oct.

Abstract

Laugier-Hunziker pigmentation (LHP) is an acquired disorder of hypermelanosis characterized by mucocutaneous hyperpigmentation. LHP may resemble various disorders characterized by mucocutaneous pigmentation. A 58-year-old lady presented with progressively increasing number of variable sized, hyperpigmented macules over the lips, fingers, toes and nails. There was no family history of similar illness. Systemic examination and all relevant investigations were within normal limits. Histopathology of a skin lesion had features consistent with LHP. The diagnosis of LHP must be made only after relevant investigations to rule out any associated systemic involvement. This case further highlights that LHP is not restricted to European countries.

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