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2024, Number 5

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Rev ADM 2024; 81 (5)

Laugier-Hunziker syndrome.

Tobón SJM, Maya GIA, Acuña GGR, Ordoñez CGC, Carrillo SJJ
Full text How to cite this article 10.35366/118114

DOI

DOI: 10.35366/118114
URL: https://dx.doi.org/10.35366/118114

Language: Spanish
References: 16
Page: 295-299
PDF size: 442.00 Kb.


Key words:

Laugier-Hunziker syndrome, idiopathic lenticular mucocutaneous pigmentation, hyperpigmentation, melanonychia.

ABSTRACT

Introduction: benign hereditary mucocutaneous hyperpigmentation with melanonychia in 2/3 of the patients. Objective: dissemination of an infrequent clinical case in oral cavity. Case presentation: patient F/18 years old attends in Diagnostic Clinic at the Faculty Dentistry, UAC 2019; with a previous diagnosis of "oral moniliasis" by Internal Medicine at five years of evolution without improvement despite multiple treatment. During the extraoral examination, macules are detected in axillary/abdomen area and intraorally, there are multiple dark brown to black macules on both cheeks, ventral, and dorsal areas of the tongue with a "whitish plaque" that superficially covers the back of the tongue. Conclusion: there are infrequent entities characterized by "white plaques" of a genetic nature in oral cavity. The knowing them avoids diagnostic error and inappropriate treatment.


REFERENCES

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Rev ADM. 2024;81