Journal of Japanese Society of Oral Medicine
Online ISSN : 2186-6155
Print ISSN : 2186-6147
ISSN-L : 2186-6147
Case Reports
Two Cases of Laugier-Hunziker Syndrome
Takuya ASAKATougo TANABETakumi SHIMURAHaruhisa WATANABEKen-ichiro SAKATANoritaka OHGAJun SATOIkuya MIYAMOTO
Author information
JOURNAL FREE ACCESS

2025 Volume 31 Issue 1 Pages 1-6

Details
Abstract
Laugier-Hunziker-Baran syndrome (LHBS) is a rare disorder characterized by multiple and melanin hyperpigmentation of the lips and oral mucosa, often associated with pigmentation of the nails and fingertips. The two patients were elderly women, in whom pigmentation of the lips, buccal mucosa and fingers was confirmed. Advance of the pigmentation was observed during long-term follow-up survey of both cases. They were systemically healthy and had no family history of abnormal pigmentation. Differential diagnosis from Addison disease and Peutz-Jeghers syndrome was ruled out. It is necessary for oral clinicians to recognize this syndrome as one of the diseases that causes oral pigmentation to develop, and to distinguish it from other cases of abnormal pigmentation.
Content from these authors
© 2025 Japanese Society of Oral Medicine
Next article
feedback
Top